US20020137179A1 - Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof - Google Patents
Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof Download PDFInfo
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- US20020137179A1 US20020137179A1 US09/813,133 US81313301A US2002137179A1 US 20020137179 A1 US20020137179 A1 US 20020137179A1 US 81313301 A US81313301 A US 81313301A US 2002137179 A1 US2002137179 A1 US 2002137179A1
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
- C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
- C12N9/6424—Serine endopeptidases (3.4.21)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention is in the field of protease proteins that are related to the carboxypeptidase subfamily, recombinant DNA molecules, and protein production.
- the present invention specifically provides novel peptides and proteins that effect protein cleavage/processing/turnover and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.
- the proteases may be categorized into families by the different amino acid sequences (generally between 2 and 10 residues) located on either side of the cleavage site of the protease.
- protease activity regulate many different cell proliferation, differentiation, and signaling processes by regulating protein turnover and processing. Uncontrolled protease activity (either increased or decreased) has been implicated in a variety of disease conditions including inflammation, cancer, arteriosclerosis, and degenerative disorders.
- proteolysis An additional role of intracellular proteolysis is in the stress-response.
- Cells that are subject to stress such as starvation, heat-shock, chemical insult or mutation respond by increasing the rates of proteolysis.
- One function of this enhanced proteolysis is to salvage amino acids from non-essential proteins. These amino acids can then be re-utilized in the synthesis of essential proteins or metabolized directly to provide energy.
- Another function is in the repair of damage caused by the stress. For example, oxidative stress has been shown to damage a variety of proteins and cause them to be rapidly degraded.
- protease for the subset of peptide bond hydrolases (Subclass E.C 3.4.).
- protease is synonymous with peptidase.
- Peptidases comprise two groups of enzymes: the endopeptidases and the exopeptidases, which cleave peptide bonds at points within the protein and remove amino acids sequentially from either N or C-terminus respectively.
- proteinase is also used as a synonym word for endopeptidase and four mechanistic classes of proteinases are recognized by the IUBMB: two of these are described below (also see: Handbook of Proteolytic Enzymes by Barrett, Rawlings, and Woessner AP Press, NY 1998). Also, for a review of the various uses of proteases as drug targets, see: Weber M, Emerging treatments for hypertension: potential role for vasopeptidase inhibition; Am J Hypertens November 1999; 12(11 Pt 2):139S-147S; Kentsch M, Otter W, Novel neurohormonal modulators in cardiovascular disorders.
- SP serine proteases
- the serine proteases are a large family of proteolytic enzymes that include the digestive enzymes, trypsin and chymotrypsin, components of the complement cascade and of the blood-clotting cascade, and enzymes that control the degradation and turnover of macromolecules of the extracellular matrix. SP are so named because of the presence of a serine residue in the active catalytic site for protein cleavage. SP have a wide range of substrate specificities and can be subdivided into subfamilies on the basis of these specificities.
- the main sub-families are trypases (cleavage after arginine or lysine), aspases (cleavage after aspartate), chymases (cleavage after phenylalanine or leucine), metases (cleavage after methionine), and serases (cleavage after serine).
- a series of six SP have been identified in murine cytotoxic T-lymphocytes (CTL) and natural killer (NK) cells. These SP are involved with CTL and NK cells in the destruction of virally transformed cells and tumor cells and in organ and tissue transplant rejection (Zunino, S. J. et al. (1990) J. Immunol. 144:2001-9; Sayers, T. J. et al. (1994) J. Immunol. 152:2289-97). Human homologs of most of these enzymes have been identified (Trapani, J. A. et al. (1988) Proc. Natl. Acad. Sci. 85:6924-28; Caputo, A. et al. (1990) J.
- the CTL-SP share three distinguishing features: 1) the presence of a catalytic triad of histidine, serine, and aspartate residues which comprise the active site; 2) the sequence GDSGGP which contains the active site serine; and 3) an N-terminal IIGG sequence which characterizes the mature SP.
- the SP are secretory proteins which contain N-terminal signal peptides that serve to export the immature protein across the endoplasmic reticulum and are then cleaved (von Heijne (1986) Nuc. Acid. Res. 14:5683-90). Differences in these signal sequences provide one means of distinguishing individual SP.
- This sequence varies in different SP according to the biochemical pathway and/or its substrate (Zunino et al, supra; Sayers et al, supra).
- Other features that distinguish various SP are the presence or absence of N-linked glycosylation sites that provide membrane anchors, the number and distribution of cysteine residues that determine the secondary structure of the SP, and the sequence of a substrate binding sites such as S′.
- the S′ substrate binding region is defined by residues extending from approximately +17 to +29 relative to the N-terminal I (+1). Differences in this region of the molecule are believed to determine SP substrate specificities (Zunino et al, supra).
- trypsinogens are serine proteases secreted by exocrine cells of the pancreas (Travis J and Roberts R. Biochemistry 1969; 8: 2884-9; Mallory P and Travis J, Biochemistry 1973; 12: 2847-51).
- trypsinogen-1 also called cationic trypsinogen
- trypsinogen-2 or anionic trypsinogen.
- the trypsinogen proenzymes are activated to trypsins in the intestine by enterokinase, which removes an activation peptide from the N-terminus of the trypsinogens.
- trypsinogens show a high degree of sequence homology, but they can be separated on the basis of charge differences by using electrophoresis or ion exchange chromatography.
- the major form of trypsinogen in the pancreas and pancreatic juice is trypsinogen-1 (Guy C O et al., Biochem Biophys Res Commun 1984; 125: 516-23).
- trypsinogen-1 In serum of healthy subjects, trypsinogen-1 is also the major form, whereas in patients with pancreatitis, trypsinogen-2 is more strongly elevated (Itkonen et al., J Lab Clin Med 1990; 115:712-8).
- Trypsinogens also occur in certain ovarian tumors, in which trypsinogen-2 is the major form (Koivunen et al., Cancer Res 1990; 50: 2375-8). Trypsin-1 in complex with alpha-1 -antitrypsin, also called alpha-1 -antiprotease, has been found to occur in serum of patients with pancreatitis (Borgstrom A and Ohlsson K, Scand J Clin Lab Invest 1984; 44: 381-6) but determination of this complex has not been found useful for differentiation between pancreatic and other gastrointestinal diseases (Borgstrom et al., Scand J Clin Lab Invest 1989; 49:757-62).
- Trypsinogen-1 and -2 are closely related immunologically (Kimland et al., Clin Chim Acta 1989; 184: 31-46; Itkonen et al., 1990), but by using monoclonal antibodies (Itkonen et al., 1990) or by absorbing polyclonal antisera (Kimland et al., 1989) it is possible to obtain reagents enabling specific measurement of each form of trypsinogen.
- AAT alpha-2-macroglobulin and alpha-1-antitrypsin
- Inflammation of the pancreas or pancreatitis may be classified as either acute or chronic by clinical criteria. With treatment, acute pancreatitis can often be cured and normal function restored. Chronic pancreatitis often results in permanent damage. The precise mechanisms which trigger acute inflammation are not understood. However, some causes in the order of their importance are alcohol ingestion, biliary tract disease, post-operative trauma, and hereditary pancreatitis. One theory provides that autodigestion, the premature activation of proteolytic enzymes in the pancreas rather than in the duodenum, causes acute pancreatitis. Any number of other factors including endotoxins, exotoxins, viral infections, ischemia, anoxia, and direct trauma may activate the proenzymes. In addition, any internal or external blockage of pancreatic ducts can also cause an accumulation of pancreatic juices in the pancreas resulting cellular damage.
- the metalloproteases may be one of the older classes of proteinases and are found in bacteria, fungi as well as in higher organisms. They differ widely in their sequences and their structures but the great majority of enzymes contain a zinc atom which is catalytically active. In some cases, zinc may be replaced by another metal such as cobalt or nickel without loss of the activity. Bacterial thermolysin has been well characterized and its crystallographic structure indicates that zinc is bound by two histidines and one glutamic acid.
- HEXXH histidine ligands for the zinc whereas the third ligand is either a glutamic acid (thermolysin, neprilysin, alanyl aminopeptidase) or a histidine (astacin).
- Other families exhibit a distinct mode of binding of the Zn atom.
- the catalytic mechanism leads to the formation of a non covalent tetrahedral intermediate after the attack of a zinc-bound water molecule on the carbonyl group of the scissile bond. This intermediate is further decomposed by transfer of the glutamic acid proton to the leaving group.
- Metalloproteases contain a catalytic zinc metal center which participates in the hydrolysis of the peptide backbone (reviewed in Power and Harper, in Protease Inhibitors, A. J. Barrett and G. Salversen (eds.) Elsevier, Amsterdam, 1986, p. 219).
- the active zinc center differentiates some of these proteases from calpains and trypsins whose activities are dependent upon the presence of calcium.
- metalloproteases include carboxypeptidase A, carboxypeptidase B, and thermolysin.
- Metalloproteases have been isolated from a number of procaryotic and eucaryotic sources, e.g. Bacillus subtilis (McConn et al., 1964, J. Biol. Chem. 239:3706); Bacillus megaterium; Serratia (Miyata et al., 1971, Agr. Biol. Chem. 35:460); Clostridium bifermentans (MacFarlane et al., 1992, App. Environ. Microbiol. 58:1195-1200), Legionella pneumophila (Moffat et al., 1994, Infection and Immunity 62:751-3).
- Bacillus subtilis McConn et al., 1964, J. Biol. Chem. 239:3706
- Serratia Microata et al., 1971, Agr. Biol. Chem. 35:460
- Clostridium bifermentans MacFarlane et al., 1992, App. Environ
- Neutral metalloproteases obtained from Aspergillus have been classified into two groups, npI and npII (Sekine, 1972, Agric. Biol. Chem. 36:207-216). So far, success in obtaining amino acid sequence information from these fungal neutral metalloproteases has been limited.
- An npII metalloprotease isolated from Aspergillus oryzae has been cloned based on amino acid sequence presented in the literature (Tatsumi et al., 1991, Mol. Gen. Genet. 228:97-103). However, to date, no npI fungal metalloprotease has been cloned or sequenced.
- Alkaline metalloproteases for example, have been isolated from Pseudomonas aeruginosa (Baumann et al., 1993, EMBO J 12:3357-3364) and the insect pathogen Xenorhabdus luminescens (Schmidt et al., 1998, Appl. Environ. Microbiol. 54:2793-2797).
- Metalloproteases have been devided into several distinct families based primarily on activity and sturcture: 1) water nucleophile; water bound by single zinc ion ligated to two His (within the motif HEXXH) and Glu, His or Asp; 2) water nucleophile; water bound by single zinc ion ligated to His, Glu (within the motif HXXE) and His; 3) water nucleophile; water bound by single zinc ion ligated to His, Asp and His; 4) Water nucleophile; water bound by single zinc ion ligated to two His (within the motif HXXEH) and Glu and 5) water nucleophile; water bound by two zinc ions ligated by Lys, Asp, Asp, Asp, Glu.
- Examples of members of the metalloproteinase family include, but are not limited to, membrane alanyl aminopeptidase ( Homo sapiens ), germinal peptidyl-dipeptidase A ( Homo sapiens ), thimet oligopeptidase ( Rattus norvegicus ), oligopeptidase F ( Lactococcus lactis ), mycolysin ( Streptomyces cacaoi ), immune inhibitor A ( Bacillus thuringiensis ), snapalysin ( Streptomyces lividans ), leishmanolysin ( Leishmania major ), microbial collagenase ( Vibrio alginolyticus ), microbial collagenase, class I ( Clostridium perfringens ), collagenase 1 ( Homo sapiens ), serralysin ( Serratia marcescens ), fragilysin ( Bacteroides fragilis ), gametolysin ( Ch
- Metalloproteases have been found to have a number of uses. For example, there is strong evidence that a metalloprotease is involved in the in vivo proteolytic processing of the vasoconstrictor, endothelin-1. Rat metalloprotease has been found to be involved in peptide hormone processing. One important subfamily of the metalloproteases are the matrix metalloproteases.
- a number of diseases are thought to be mediated by excess or undesired metalloprotease activity or by an imbalance in the ratio of the various members of the protease family of proteins. These include: a) osteoarthritis (Woessner, et al., J. Biol.Chem. 259(6), 3633, 1984; Phadke, et al., J. Rheumatol. 10, 852, 1983), b) rheumatoid arthritis (Mullins, et al., Biochim. Biophys. Acta 695, 117, 1983; Woolley, et al., Arthritis Rheum.
- Aspartic proteases have been divided into several distinct families based primarily on activity and structure. These include 1) water nucleophile; water bound by two Asp from monomer or dimer; all endopeptidases, from eukaryote organisms, viruses or virus-like organisms and 2) endopeptidases that are water nucleophile and are water bound by Asp and Asn.
- aspartic proteases belong to the pepsin family.
- the pepsin family includes digestive enzymes such as pepsin and chymosin as well as lysosomal cathepsins D and processing enzymes such as renin, and certain fungal proteases (penicillopepsin, rhizopuspepsin, endothiapepsin).
- a second family comprises viral proteases such as the protease from the AIDS virus (HIV) also called retropepsin. Crystallographic studies have shown that these enzymes are bilobed molecules with the active site located between two homologous lobes. Each lobe contributes one aspartate residue of the catalytically active diad of aspartates.
- Retropepsins are monomeric, i.e carry only one catalytic aspartate and then dimerization is required to form an active enzyme.
- aspartic protease family of proteins include, but are not limited to, pepsin A ( Homo sapiens ), HIV1 retropepsin (human immunodeficiency virus type 1), endopeptidase (cauliflower mosaic virus), bacilliform virus putative protease (rice tungro bacilliform virus), aspergillopepsin II ( Aspergillus niger ), thermopsin ( Sulfolobus acidocaldarius ), nodavirus endopeptidase (flock house virus), pseudomonapepsin (Pseudomonas sp.
- pepsin A Homo sapiens
- HIV1 retropepsin human immunodeficiency virus type 1
- endopeptidase cauliflower mosaic virus
- bacilliform virus putative protease rice tungro bacilliform virus
- aspergillopepsin II Aspergillus niger
- thermopsin S
- signal peptidase II Escherichia coli
- polyprotein peptidase human spumaretrovirus
- copia transposon Drosophila melanogaster
- SIRE-1 peptidase Glycine max
- retrotransposon bs1 endopeptidase Zea mays
- retrotransposon peptidase Drosophila buzzatii
- Tas retrotransposon peptidase Ascaris lumbricoides
- Pao retrotransposon peptidase Bombyx mori
- putative proteinase of Skippy retrotransposon Fusarium oxysporum
- tetravirus endopeptidase Nudaurelia capensis omega virus
- presenilin 1 Homo sapiens
- Carboxypeptidases are proteases that function in many physiological processes. These proteases remove a wide range of carboxyl-terminal amino acids, and in doing so are able to activate, inactivate, and modulate enzyme and peptide hormone activity. Many active forms of mammalian carboxypeptidases are located in lysosomes where they regulate intracellular protein processing, degradation and turnover. In plants and insects carboxypeptidases play a role in posttranslational protein modifications including mobilization of storage proteins and hormone activation.
- Carboxypeptidase activities are regulated either by endogenous protein inhibitors or by enzymatic cleavage of a segment of a propeptide to release the active carboxypeptidase.
- Carboxypeptidases A and B are pancreatic zinc-containing proteolytic enzymes which catalyze the hydrolysis of the carboxyl-terminal peptide bond in polypeptide chains. When transcribed in rat brain and other nonpancreatic tissues, CPA is unable to function as a protease (Normant, E. et al. (1995) J. Biol. Chem. 270: 20543-20549).
- tissue-specific, endogenous protein inhibitors such as tissue carboxypeptidase inhibitor (TCI) or latexin (Normant, E. et al. (1995) Proc. Natl. Acad. Sci. 92: 12225-12229; Hatanaka, Y. et al. (1994) Eur. J. Neurosci. 6: 973-982).
- Latexin and TCI are 222 and 223 amino acids in length, respectively. They contain several potential phosphorylation sites, but they do not show a membrane-specific signal peptide sequence (Normant et al., supra; Hatanaka et al., supra). TCI is a non-competitive, nearly irreversible, and potent inhibitor of CPA; it is less potent against CPB and does not act on various other proteases. TCI and latexin are both expressed and localized in the cytosol of a number of tissues including brain, lung, or digestive tract. It has been suggested that TCI or latexin may function in regulating tissue-specific, cytosolic protein degradation (Normant et al., supra).
- carboxypeptidase B inhibitor DL-5-guanidinoethylmercaptosuccinic acid.
- Tsai and Drayna (1992) used PCR to identify the presence of the plasma carboxypeptidase B gene in somatic hybrid cell lines which is called carboxypeptidase B2 (CPB2), also called carboxypeptidase U (CPU). It is an unstable basic carboxypeptidase that circulates in human plasma in its proenzyme form.
- pro-CPU The most likely physiologic activator of pro-CPU is the thrombin-thrombomodulin complex. Vanhoof et al. (1996) noted that pro-CPU exhibits affinity for plasminogen and can be converted to its active form through the action of thrombin and plasmin. CPB2 gene is located on human chromosome 13. To regionalize the assignment of the gene on chromosome 13, Vanhoof et al. (1996) used fluorescence in situ hybridization. They found that it is localized to 13q14.11.
- the protein of the present invention has a substantial similarity to the carboxypeptidase B as set forth above.
- Protease proteins particularly members of the carboxypeptidase subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of protease proteins.
- the present invention advances the state of the art by providing a previously unidentified human protease proteins that have homology to members of the carboxypeptidase subfamily.
- the present invention is based in part on the identification of amino acid sequences of human protease peptides and proteins that are related to the carboxypeptidase subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate protease activity in cells and tissues that express the protease. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- FIG. 1 provides the nucleotide sequence of a cDNA molecule or transcript sequence that encodes the protease protein of the present invention. (SEQ ID NO:1)
- structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- FIG. 2 provides the predicted amino acid sequence of the protease of the present invention. (SEQ ID NO:2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- FIG. 3 provides genomic sequences that span the gene encoding the protease protein of the present invention. (SEQ ID NO:3)
- structure and functional information such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- SNPs including insertion/deletion variants (“indels”), were identified at 40 different nucleotide positions.
- the present invention is based on the sequencing of the human genome.
- sequencing and assembly of the human genome analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a protease protein or part of a protease protein and are related to the carboxypeptidase subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized.
- the present invention provides amino acid sequences of human protease peptides and proteins that are related to the carboxypeptidase subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these protease peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the protease of the present invention.
- the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known protease proteins of the carboxypeptidase subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene.
- the present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the protease family of proteins and are related to the carboxypeptidase subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3).
- the peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the protease peptides of the present invention, protease peptides, or peptides/proteins of the present invention.
- the present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the protease peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.
- a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals.
- the peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).
- substantially free of cellular material includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins.
- the peptide when it is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.
- the language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the protease peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.
- the isolated protease peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- a nucleic acid molecule encoding the protease peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell.
- the protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.
- the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- the amino acid sequence of such a protein is provided in FIG. 2.
- a protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.
- the present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- a protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.
- the present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- a protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids.
- the preferred classes of proteins that are comprised of the protease peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.
- the protease peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins.
- Such chimeric and fusion proteins comprise a protease peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the protease peptide. “Operatively linked” indicates that the protease peptide and the heterologous protein are fused in-frame.
- the heterologous protein can be fused to the N-terminus or C-terminus of the protease peptide.
- the fusion protein does not affect the activity of the protease peptide per se.
- the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions.
- Such fusion proteins, particularly poly-His fusions can facilitate the purification of recombinant protease peptide.
- expression and/or secretion of a protein can be increased by using a heterologous signal sequence.
- a chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques.
- the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al., Current Protocols in Molecular Biology, 1992).
- many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein).
- a protease peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the protease peptide.
- the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides.
- variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.
- variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the protease peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.
- the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes).
- at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes.
- the amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared.
- amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”.
- the percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.
- the percent identity between two amino acid sequences is determined using the Needleman and Wunsch ( J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6.
- the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) (available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6.
- the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.
- the nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences.
- Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. ( J. Mol. Biol. 215:403-10 (1990)).
- Gapped BLAST can be utilized as described in Altschul et al. ( Nucleic Acids Res. 25(17):3389-3402 (1997)).
- the default parameters of the respective programs e.g., XBLAST and NBLAST
- XBLAST and NBLAST can be used.
- Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the protease peptides of the present invention as well as being encoded by the same genetic locus as the protease peptide provided herein. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- allelic variants of a protease peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the protease peptide as well as being encoded by the same genetic locus as the protease peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- two proteins have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous.
- a significantly homologous amino acid sequence will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under stringent conditions as more fully described below.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention.
- 40 SNP variants were found, including 5 indels (indicated by a “ ⁇ ”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs).
- SNPs, identified at different nucleotide positions in introns and regions 5′ and 3′ of the ORF, may affect control/regulatory elements.
- Paralogs of a protease peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the protease peptide, as being encoded by a gene from humans, and as having similar activity or function.
- Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain.
- Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.
- orthologs of a protease peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the protease peptide as well as being encoded by a gene from another organism.
- Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents.
- Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention.
- 40 SNP variants were found, including 5 indels (indicated by a “ ⁇ ”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs).
- SNPs, identified at different nucleotide positions in introns and regions 5′ and 3′ of the ORF, may affect control/regulatory elements.
- Non-naturally occurring variants of the protease peptides of the present invention can readily be generated using recombinant techniques.
- Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the protease peptide.
- one class of substitutions are conserved amino acid substitution.
- Such substitutions are those that substitute a given amino acid in a protease peptide by another amino acid of like characteristics.
- conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr.
- Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al., Science 247:1306-1310 (1990).
- Variant protease peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to cleave substrate, ability to participate in a signaling pathway, etc.
- Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions.
- FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions.
- Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.
- Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.
- Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al., Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as protease activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al, J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).
- the present invention further provides fragments of the protease peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2.
- the fragments to which the invention pertains are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.
- a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a protease peptide.
- Such fragments can be chosen based on the ability to retain one or more of the biological activities of the protease peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen.
- Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length.
- Such fragments will typically comprise a domain or motif of the protease peptide, e.g., active site, a transmembrane domain or a substrate-binding domain.
- fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures.
- Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.
- Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in protease peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).
- Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.
- the protease peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature protease peptide is fused with another compound, such as a compound to increase the half-life of the protease peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature protease peptide, such as a leader or secretory sequence or a sequence for purification of the mature protease peptide or a pro-protein sequence.
- a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature protease peptide is fused with another compound, such as a compound to increase the half-life of the protease peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature protease peptide, such as a leader
- the proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state).
- the protein binds or potentially binds to another protein or ligand (such as, for example, in a protease-effector protein interaction or protease-ligand interaction)
- the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.
- proteases isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the protease.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver.
- the proteins of the present invention are useful for biological assays related to proteases that are related to members of the carboxypeptidase subfamily.
- Such assays involve any of the known protease functions or activities or properties useful for diagnosis and treatment of protease-related conditions that are specific for the subfamily of proteases that the one of the present invention belongs to, particularly in cells and tissues that express the protease.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver.
- the proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems.
- Cell-based systems can be native, i.e., cells that normally express the protease, as a biopsy or expanded in cell culture.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- cell-based assays involve recombinant host cells expressing the protease protein.
- the polypeptides can be used to identify compounds that modulate protease activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the protease.
- Both the proteases of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the protease. These compounds can be further screened against a functional protease to determine the effect of the compound on the protease activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the protease to a desired degree.
- the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the protease protein and a molecule that normally interacts with the protease protein, e.g. a substrate or a component of the signal pathway that the protease protein normally interacts (for example, a protease).
- a molecule that normally interacts with the protease protein e.g. a substrate or a component of the signal pathway that the protease protein normally interacts (for example, a protease).
- Such assays typically include the steps of combining the protease protein with a candidate compound under conditions that allow the protease protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the protease protein and the target, such as any of the associated effects of signal transduction such as protein cleavage, cAMP turnover, and adenylate cyclase activation, etc.
- Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L-configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′) 2 , Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic
- One candidate compound is a soluble fragment of the receptor that competes for substrate binding.
- Other candidate compounds include mutant proteases or appropriate fragments containing mutations that affect protease function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.
- the invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) protease activity.
- the assays typically involve an assay of events in the signal transduction pathway that indicate protease activity.
- the cleavage of a substrate, inactivation/activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the protease protein dependent signal cascade can be assayed.
- any of the biological or biochemical functions mediated by the protease can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the protease can be assayed. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver.
- Binding and/or activating compounds can also be screened by using chimeric protease proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions.
- a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native protease. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the protease is derived.
- the proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the protease (e.g. binding partners and/or ligands).
- a compound is exposed to a protease polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide.
- Soluble protease polypeptide is also added to the mixture. If the test compound interacts with the soluble protease polypeptide, it decreases the amount of complex formed or activity from the protease target.
- This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the protease.
- the soluble polypeptide that competes with the target protease region is designed to contain peptide sequences corresponding to the region of interest.
- a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix.
- glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtiter plates, which are then combined with the cell lysates (e.g., 35 S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH).
- the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated.
- the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of protease-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques.
- the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art.
- antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation.
- Preparations of a protease-binding protein and a candidate compound are incubated in the protease protein-presenting wells and the amount of complex trapped in the well can be quantitated.
- Methods for detecting such complexes include immunodetection of complexes using antibodies reactive with the protease protein target molecule, or which are reactive with protease protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.
- Agents that modulate one of the proteases of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.
- Modulators of protease protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the protease pathway, by treating cells or tissues that express the protease.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- These methods of treatment include the steps of administering a modulator of protease activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.
- the protease proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al (1993) Cell 72:223-232; Madura et al (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al.
- protease-binding proteins are also likely to be involved in the propagation of signals by the protease proteins or protease targets as, for example, downstream elements of a protease-mediated signaling pathway.
- protease-binding proteins are likely to be protease inhibitors.
- the two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains.
- the assay utilizes two different DNA constructs.
- the gene that codes for a protease protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4).
- a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor.
- the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the protease protein.
- a reporter gene e.g., LacZ
- This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model.
- an agent identified as described herein e.g., a protease-modulating agent, an antisense protease nucleic acid molecule, a protease-specific antibody, or a protease-binding partner
- an agent identified as described herein can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent.
- an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent.
- this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.
- the protease proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The method involves contacting a biological sample with a compound capable of interacting with the protease protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein.
- a biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.
- the peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs.
- the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification.
- Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered protease activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein.
- Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- peptide detection techniques include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent.
- a detection reagent such as an antibody or protein binding agent.
- the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent.
- the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.
- the peptides are also useful in pharmacogenomic analysis.
- Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. ( Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. ( Clin. Chem. 43(2):254-266 (1997)).
- the clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism.
- the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound.
- the activity of drug metabolizing enzymes effects both the intensity and duration of drug action.
- the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype.
- the discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the protease protein in which one or more of the protease functions in one population is different from those in another population.
- polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and protease activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism.
- genotyping specific polymorphic peptides could be identified.
- the peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. Accordingly, methods for treatment include the use of the protease protein or fragments.
- the invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof.
- an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins.
- An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.
- an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge.
- the antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′) 2 , and Fv fragments.
- an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse.
- a mammalian organism such as a rat, rabbit or mouse.
- the full-length protein, an antigenic peptide fragment or a fusion protein can be used.
- Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.
- Antibodies are preferably prepared from regions or discrete fragments of the protease proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or protease/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.
- An antigenic fragment will typically comprise at least 8 contiguous amino acid residues.
- the antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues.
- Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).
- Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance.
- detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials.
- suitable enzymes include horseradish peroxidase, alkaline phosphatase, ⁇ -galactosidase, or acetylcholinesterase;
- suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin;
- suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin;
- an example of a luminescent material includes luminol;
- examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include 125 I, 131 I, 35 S or 3 H.
- the antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation.
- the antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells.
- such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver.
- antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.
- the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function.
- a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form
- the antibody can be prepared against the normal protein.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.
- the antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- the diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.
- antibodies are useful in pharmacogenomic analysis.
- antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities.
- the antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.
- the antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.
- the antibodies are also useful for inhibiting protein function, for example, blocking the binding of the protease peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function.
- An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity.
- Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.
- kits for using antibodies to detect the presence of a protein in a biological sample can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use.
- a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nucleic acid arrays and similar methods have been developed for antibody arrays.
- the present invention further provides isolated nucleic acid molecules that encode a protease peptide or protein of the present invention (cDNA, transcript and genomic sequence).
- Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the protease peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.
- an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid.
- an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived.
- flanking nucleotide sequences for example up to about 5 KB, 4 KB, 3 KB, 2 KB, or 1 KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence.
- flanking nucleotide sequences for example up to about 5 KB, 4 KB, 3 KB, 2 KB, or 1 KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence.
- an “isolated” nucleic acid molecule such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized.
- the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.
- recombinant DNA molecules contained in a vector are considered isolated.
- isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution.
- isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention.
- Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.
- nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.
- the present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.
- the present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule.
- the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences.
- Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.
- FIGS. 1 and 3 both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.
- the isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.
- the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the protease peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA.
- the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.
- Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof.
- the nucleic acid, especially DNA can be double-stranded or single-stranded.
- Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).
- the invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the protease proteins of the present invention that are described above.
- nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis.
- Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.
- the present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3.
- Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents.
- a promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.
- a fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.
- a probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair.
- the oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.
- Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene.
- hybridizes under stringent conditions is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other.
- the conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other.
- stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6.
- stringent hybridization conditions are hybridization in 6 ⁇ sodium chloride/sodium citrate (SSC) at about 45 C, followed by one or more washes in 0.2 ⁇ SSC, 0.1% SDS at 50-65 C.
- SSC 6 ⁇ sodium chloride/sodium citrate
- washes in 0.2 ⁇ SSC, 0.1% SDS at 50-65 C.
- moderate to low stringency hybridization conditions are well known in the art.
- the nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays.
- the nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2.
- SNPs including insertion/deletion variants (“indels”), were identified at 40 different nucleotide positions.
- the probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.
- the nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.
- the nucleic acid molecules are also useful for constructing recombinant vectors.
- Such vectors include expression vectors that express a portion of, or all of, the peptide sequences.
- Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product.
- an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.
- nucleic acid molecules are also useful for expressing antigenic portions of the proteins.
- the nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.
- nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.
- nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.
- nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.
- the nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.
- the nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms.
- the nucleic acid whose level is determined can be DNA or RNA.
- probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in protease protein expression relative to normal results.
- In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations.
- In vitro techniques for detecting DNA includes Southern hybridizations and in situ hybridization.
- Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a protease protein, such as by measuring a level of a protease-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a protease gene has been mutated.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver.
- Nucleic acid expression assays are useful for drug screening to identify compounds that modulate protease nucleic acid expression.
- the invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the protease gene, particularly biological and pathological processes that are mediated by the protease in cells and tissues that express it.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- the method typically includes assaying the ability of the compound to modulate the expression of the protease nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired protease nucleic acid expression.
- the assays can be performed in cell-based and cell-free systems.
- Cell-based assays include cells naturally expressing the protease nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.
- the assay for protease nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the protease protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.
- modulators of protease gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined.
- the level of expression of protease mRNA in the presence of the candidate compound is compared to the level of expression of protease mRNA in the absence of the candidate compound.
- the candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression.
- expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression.
- nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.
- the invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate protease nucleic acid expression in cells and tissues that express the protease.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.
- a modulator for protease nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the protease nucleic acid expression in the cells and tissues that express the protein.
- Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- the nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the protease gene in clinical trials or in a treatment regimen.
- the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance.
- the gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.
- the nucleic acid molecules are also useful in diagnostic assays for qualitative changes in protease nucleic acid expression, and particularly in qualitative changes that lead to pathology.
- the nucleic acid molecules can be used to detect mutations in protease genes and gene expression products such as mRNA.
- the nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the protease gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the protease gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a protease protein.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “ ⁇ ”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and regions 5′ and 3′ of the ORF, may affect control/regulatory elements. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis.
- RNA or cDNA can be used in the same way.
- detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos.
- PCR polymerase chain reaction
- This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences.
- nucleic acid e.g., genomic, mRNA or both
- mutations in a protease gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.
- sequence-specific ribozymes can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.
- Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method. Furthermore, sequence differences between a mutant protease gene and a wild-type gene can be determined by direct DNA sequencing.
- a variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995) Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. Biotechnol. 38:147-159 (1993)).
- Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al., Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl.
- the nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality.
- the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship).
- the nucleic acid molecules described herein can be used to assess the mutation content of the protease gene in an individual in order to select an appropriate compound or dosage regimen for treatment.
- nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.
- the nucleic acid molecules are thus useful as antisense constructs to control protease gene expression in cells, tissues, and organisms.
- a DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of protease protein.
- An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into protease protein.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention.
- SNP variants were found, including 5 indels (indicated by a “ ⁇ ”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and regions 5′ and 3′ of the ORF, may affect control/regulatory elements.
- a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of protease nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired protease nucleic acid expression.
- This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the protease protein, such as substrate binding.
- the nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in protease gene expression.
- recombinant cells which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired protease protein to treat the individual.
- the invention also encompasses kits for detecting the presence of a protease nucleic acid in a biological sample.
- Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot.
- PCR-based tissue screening panel indicates expression in whole liver.
- the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting protease nucleic acid in a biological sample; means for determining the amount of protease nucleic acid in the sample; and means for comparing the amount of protease nucleic acid in the sample with a standard.
- the compound or agent can be packaged in a suitable container.
- the kit can further comprise instructions for using the kit to detect protease protein mRNA or DNA.
- the present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).
- Arrays or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support.
- the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application W095/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93 : 10614-10619), all of which are incorporated herein in their entirety by reference.
- such arrays are produced by the methods described by Brown et al., U.S. Pat. No. 5,807,522.
- the microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support.
- the oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length.
- the microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence.
- Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.
- the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit.
- the “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence.
- the second oligonucleotide in the pair serves as a control.
- the number of oligonucleotide pairs may range from two to one million.
- the oligomers are synthesized at designated areas on a substrate using a light-directed chemical process.
- the substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.
- an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application W095/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference.
- a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures.
- An array such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.
- RNA or DNA from a biological sample is made into hybridization probes.
- the mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA).
- aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence.
- the scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit.
- the biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations.
- a detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.
- the present invention provides methods to identify the expression of the protease proteins/peptides of the present invention.
- methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample.
- assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the protease gene of the present invention.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention.
- SNP variants were found, including 5 indels (indicated by a “ ⁇ ”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and regions 5′ and 3′ of the ORF, may affect control/regulatory elements.
- Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T, An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).
- test samples of the present invention include cells, protein or membrane extracts of cells.
- the test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.
- kits which contain the necessary reagents to carry out the assays of the present invention.
- the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.
- a compartmentalized kit includes any kit in which reagents are contained in separate containers.
- Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica.
- Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another.
- Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe.
- wash reagents such as phosphate buffered saline, Tris-buffers, etc.
- the invention also provides vectors containing the nucleic acid molecules described herein.
- the term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules.
- the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid.
- the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.
- a vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules.
- the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.
- the invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules.
- the vectors can function in prokaryotic or eukaryotic cells or in both (shuttle vectors).
- Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell.
- the nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription.
- the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector.
- a trans-acting factor may be supplied by the host cell.
- a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.
- the regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage ⁇ , the lac, TRP, and TAC promoters from E. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.
- expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers.
- regions that modulate transcription include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.
- expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation.
- Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals.
- the person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- a variety of expression vectors can be used to express a nucleic acid molecule.
- Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses.
- Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g.
- the regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand.
- host cells i.e. tissue specific
- inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand.
- a variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.
- the nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology.
- the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.
- the vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques.
- Bacterial cells include, but are not limited to, E. coli, Streptomyces, and Salmonella typhimurium.
- Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.
- the invention provides fusion vectors that allow for the production of the peptides.
- Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification.
- a proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety.
- Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enteroprotease.
- Typical fusion expression vectors include pGEX (Smith et al., Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein.
- GST glutathione S-transferase
- suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).
- Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein.
- the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al., Nucleic Acids Res. 20:2111-2118 (1992)).
- the nucleic acid molecules can also be expressed by expression vectors that are operative in yeast.
- yeast e.g., S. cerevisiae
- vectors for expression in yeast include pYepSec1 (Baldari, et al., EMBO J. 6:229-234 (1987)), pMFa (Kujan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).
- the nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors.
- Baculovirus vectors available for expression of proteins in cultured insect cells include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 170:31-39 (1989)).
- the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors.
- mammalian expression vectors include pCDM8 (Seed, B. Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J. 6:187-195 (1987)).
- the expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules.
- the person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.
- the invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA.
- an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).
- the invention also relates to recombinant host cells containing the vectors described herein.
- Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.
- the recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. ( Molecular Cloning: A Laboratory Manual. 2nd, ed, Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).
- Host cells can contain more than one vector.
- different nucleotide sequences can be introduced on different vectors of the same cell.
- the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors.
- the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.
- bacteriophage and viral vectors these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction.
- Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.
- Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs.
- the marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.
- the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.
- secretion signals are incorporated into the vector.
- the signal sequence can be endogenous to the peptides or heterologous to these peptides.
- the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like.
- the peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatite chromatography, lectin chromatography, or high performance liquid chromatography.
- the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria.
- the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.
- the recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a protease protein or peptide that can be further purified to produce desired amounts of protease protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.
- Host cells are also useful for conducting cell-based assays involving the protease protein or protease protein fragments, such as those described above as well as other formats known in the art.
- a recombinant host cell expressing a native protease protein is useful for assaying compounds that stimulate or inhibit protease protein function.
- Host cells are also useful for identifying protease protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant protease protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native protease protein.
- a transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene.
- a transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a protease protein and identifying and evaluating modulators of protease protein activity.
- Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.
- a transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal.
- Any of the protease protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.
- Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included.
- a tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the protease protein to particular cells.
- transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals.
- a transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals.
- transgenic founder animal can then be used to breed additional animals carrying the transgene.
- transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes.
- a transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.
- transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene.
- a system is the cre/loxP recombinase system of bacteriophage P1.
- cre/loxP recombinase system of bacteriophage P1.
- a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991).
- mice containing transgenes encoding both the Cre recombinase and a selected protein is required.
- Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.
- Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669.
- a cell e.g., a somatic cell
- the quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated.
- the reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal.
- the offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.
- Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, protease protein activity/activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo protease protein function, including substrate interaction, the effect of specific mutant protease proteins on protease protein function and substrate interaction, and the effect of chimeric protease proteins. It is also possible to assess the effect of null mutations, that is mutations that substantially or completely eliminate one or more protease protein functions.
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Abstract
Description
- The present invention is in the field of protease proteins that are related to the carboxypeptidase subfamily, recombinant DNA molecules, and protein production. The present invention specifically provides novel peptides and proteins that effect protein cleavage/processing/turnover and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.
- The proteases may be categorized into families by the different amino acid sequences (generally between 2 and 10 residues) located on either side of the cleavage site of the protease.
- The proper functioning of the cell requires careful control of the levels of important structural proteins, enzymes, and regulatory proteins. One of the ways that cells can reduce the steady state level of a particular protein is by proteolytic degradation. Further, one of the ways cells produce functioning proteins is to produce pre or pro-protein precursors that are processed by proteolytic degradation to produce an active moiety. Thus, complex and highly-regulated mechanisms have been evolved to accomplish this degradation.
- Proteases regulate many different cell proliferation, differentiation, and signaling processes by regulating protein turnover and processing. Uncontrolled protease activity (either increased or decreased) has been implicated in a variety of disease conditions including inflammation, cancer, arteriosclerosis, and degenerative disorders.
- An additional role of intracellular proteolysis is in the stress-response. Cells that are subject to stress such as starvation, heat-shock, chemical insult or mutation respond by increasing the rates of proteolysis. One function of this enhanced proteolysis is to salvage amino acids from non-essential proteins. These amino acids can then be re-utilized in the synthesis of essential proteins or metabolized directly to provide energy. Another function is in the repair of damage caused by the stress. For example, oxidative stress has been shown to damage a variety of proteins and cause them to be rapidly degraded.
- The International Union of Biochemistry and Molecular Biology (IUBMB) has recommended to use the term peptidase for the subset of peptide bond hydrolases (Subclass E.C 3.4.). The widely used term protease is synonymous with peptidase. Peptidases comprise two groups of enzymes: the endopeptidases and the exopeptidases, which cleave peptide bonds at points within the protein and remove amino acids sequentially from either N or C-terminus respectively. The term proteinase is also used as a synonym word for endopeptidase and four mechanistic classes of proteinases are recognized by the IUBMB: two of these are described below (also see:Handbook of Proteolytic Enzymes by Barrett, Rawlings, and Woessner AP Press, NY 1998). Also, for a review of the various uses of proteases as drug targets, see: Weber M, Emerging treatments for hypertension: potential role for vasopeptidase inhibition; Am J Hypertens November 1999; 12(11 Pt 2):139S-147S; Kentsch M, Otter W, Novel neurohormonal modulators in cardiovascular disorders. The therapeutic potential of endopeptidase inhibitors, Drugs R D April 1999; 1(4):331-8; Scarborough R M, Coagulation factor Xa: the prothrombinase complex as an emerging therapeutic target for small molecule inhibitors, J Enzym Inhib 1998; 14(1):15-25; Skotnicki J S, et al., Design and synthetic considerations of matrix metalloproteinase inhibitors, Ann N Y Acad Sci June 1999 30; 878:61-72; McKerrow J H, Engel J C, Caffrey C R, Cysteine protease inhibitors as chemotherapy for parasitic infections, Bioorg Med Chem April 1999; 7(4):639-44; Rice K D, Tanaka R D, Katz B A, Numerof R P, Moore W R, Inhibitors of tryptase for the treatment of mast cell-mediated diseases, Curr Pharm Des October 1998; 4(5):381-96; Materson B J, Will angiotensin converting enzyme genotype, receptor mutation identification, and other miracles of molecular biology permit reduction of NNT Am J Hypertens August 1998; 11(8 Pt 2):138S-142S
- Serine Proteases
- The serine proteases (SP) are a large family of proteolytic enzymes that include the digestive enzymes, trypsin and chymotrypsin, components of the complement cascade and of the blood-clotting cascade, and enzymes that control the degradation and turnover of macromolecules of the extracellular matrix. SP are so named because of the presence of a serine residue in the active catalytic site for protein cleavage. SP have a wide range of substrate specificities and can be subdivided into subfamilies on the basis of these specificities. The main sub-families are trypases (cleavage after arginine or lysine), aspases (cleavage after aspartate), chymases (cleavage after phenylalanine or leucine), metases (cleavage after methionine), and serases (cleavage after serine).
- A series of six SP have been identified in murine cytotoxic T-lymphocytes (CTL) and natural killer (NK) cells. These SP are involved with CTL and NK cells in the destruction of virally transformed cells and tumor cells and in organ and tissue transplant rejection (Zunino, S. J. et al. (1990) J. Immunol. 144:2001-9; Sayers, T. J. et al. (1994) J. Immunol. 152:2289-97). Human homologs of most of these enzymes have been identified (Trapani, J. A. et al. (1988) Proc. Natl. Acad. Sci. 85:6924-28; Caputo, A. et al. (1990) J. Immunol. 145:737-44). Like all SP, the CTL-SP share three distinguishing features: 1) the presence of a catalytic triad of histidine, serine, and aspartate residues which comprise the active site; 2) the sequence GDSGGP which contains the active site serine; and 3) an N-terminal IIGG sequence which characterizes the mature SP.
- The SP are secretory proteins which contain N-terminal signal peptides that serve to export the immature protein across the endoplasmic reticulum and are then cleaved (von Heijne (1986) Nuc. Acid. Res. 14:5683-90). Differences in these signal sequences provide one means of distinguishing individual SP. Some SP, particularly the digestive enzymes, exist as inactive precursors or preproenzymes, and contain a leader or
activation peptide sequence 3′ of the signal peptide. This activation peptide may be 2-12 amino acids in length, and it extends from the cleavage site of the signal peptide to the N-terminal IIGG sequence of the active, mature protein. Cleavage of this sequence activates the enzyme. This sequence varies in different SP according to the biochemical pathway and/or its substrate (Zunino et al, supra; Sayers et al, supra). Other features that distinguish various SP are the presence or absence of N-linked glycosylation sites that provide membrane anchors, the number and distribution of cysteine residues that determine the secondary structure of the SP, and the sequence of a substrate binding sites such as S′. The S′ substrate binding region is defined by residues extending from approximately +17 to +29 relative to the N-terminal I (+1). Differences in this region of the molecule are believed to determine SP substrate specificities (Zunino et al, supra). - Trypsinogens
- The trypsinogens are serine proteases secreted by exocrine cells of the pancreas (Travis J and Roberts R. Biochemistry 1969; 8: 2884-9; Mallory P and Travis J, Biochemistry 1973; 12: 2847-51). Two major types of trypsinogen isoenzymes have been characterized, trypsinogen-1, also called cationic trypsinogen, and trypsinogen-2 or anionic trypsinogen. The trypsinogen proenzymes are activated to trypsins in the intestine by enterokinase, which removes an activation peptide from the N-terminus of the trypsinogens. The trypsinogens show a high degree of sequence homology, but they can be separated on the basis of charge differences by using electrophoresis or ion exchange chromatography. The major form of trypsinogen in the pancreas and pancreatic juice is trypsinogen-1 (Guy C O et al., Biochem Biophys Res Commun 1984; 125: 516-23). In serum of healthy subjects, trypsinogen-1 is also the major form, whereas in patients with pancreatitis, trypsinogen-2 is more strongly elevated (Itkonen et al., J Lab Clin Med 1990; 115:712-8). Trypsinogens also occur in certain ovarian tumors, in which trypsinogen-2 is the major form (Koivunen et al., Cancer Res 1990; 50: 2375-8). Trypsin-1 in complex with alpha-1 -antitrypsin, also called alpha-1 -antiprotease, has been found to occur in serum of patients with pancreatitis (Borgstrom A and Ohlsson K, Scand J Clin Lab Invest 1984; 44: 381-6) but determination of this complex has not been found useful for differentiation between pancreatic and other gastrointestinal diseases (Borgstrom et al., Scand J Clin Lab Invest 1989; 49:757-62).
- Trypsinogen-1 and -2 are closely related immunologically (Kimland et al., Clin Chim Acta 1989; 184: 31-46; Itkonen et al., 1990), but by using monoclonal antibodies (Itkonen et al., 1990) or by absorbing polyclonal antisera (Kimland et al., 1989) it is possible to obtain reagents enabling specific measurement of each form of trypsinogen.
- When active trypsin reaches the blood stream, it is inactivated by the major trypsin inhibitors alpha-2-macroglobulin and alpha-1-antitrypsin (AAT). AAT is a 58 kilodalton serine protease inhibitor synthesized in the liver and is one of the main protease inhibitors in blood. Whereas complexes between trypsin-1 and AAT are detectable in serum (Borgstrom and Ohlsson, 1984) the complexes with alpha-2-macroglobulin are not measurable with antibody-based assays (Ohlsson K, Acta Gastroenterol Belg 1988; 51: 3-12).
- Inflammation of the pancreas or pancreatitis may be classified as either acute or chronic by clinical criteria. With treatment, acute pancreatitis can often be cured and normal function restored. Chronic pancreatitis often results in permanent damage. The precise mechanisms which trigger acute inflammation are not understood. However, some causes in the order of their importance are alcohol ingestion, biliary tract disease, post-operative trauma, and hereditary pancreatitis. One theory provides that autodigestion, the premature activation of proteolytic enzymes in the pancreas rather than in the duodenum, causes acute pancreatitis. Any number of other factors including endotoxins, exotoxins, viral infections, ischemia, anoxia, and direct trauma may activate the proenzymes. In addition, any internal or external blockage of pancreatic ducts can also cause an accumulation of pancreatic juices in the pancreas resulting cellular damage.
- Anatomy, physiology, and diseases of the pancreas are reviewed, inter alia, in Guyton A C (1991) Textbook of Medical Physiology, W B Saunders Co, Philadelphia, Pa.; Isselbacher K J et al (1994) Harrison's Principles of Internal Medicine, McGraw-Hill, New York City; Johnson K E (1991) Histology and Cell Biology, Harwal Publishing, Media, Pa.; and The Merck Manual of Diagnosis and Therapy (1992) Merck Research Laboratories, Rahway, N.J.
- Metalloprotease
- The metalloproteases may be one of the older classes of proteinases and are found in bacteria, fungi as well as in higher organisms. They differ widely in their sequences and their structures but the great majority of enzymes contain a zinc atom which is catalytically active. In some cases, zinc may be replaced by another metal such as cobalt or nickel without loss of the activity. Bacterial thermolysin has been well characterized and its crystallographic structure indicates that zinc is bound by two histidines and one glutamic acid. Many enzymes contain the sequence HEXXH, which provides two histidine ligands for the zinc whereas the third ligand is either a glutamic acid (thermolysin, neprilysin, alanyl aminopeptidase) or a histidine (astacin). Other families exhibit a distinct mode of binding of the Zn atom. The catalytic mechanism leads to the formation of a non covalent tetrahedral intermediate after the attack of a zinc-bound water molecule on the carbonyl group of the scissile bond. This intermediate is further decomposed by transfer of the glutamic acid proton to the leaving group.
- Metalloproteases contain a catalytic zinc metal center which participates in the hydrolysis of the peptide backbone (reviewed in Power and Harper, in Protease Inhibitors, A. J. Barrett and G. Salversen (eds.) Elsevier, Amsterdam, 1986, p. 219). The active zinc center differentiates some of these proteases from calpains and trypsins whose activities are dependent upon the presence of calcium. Examples of metalloproteases include carboxypeptidase A, carboxypeptidase B, and thermolysin.
- Metalloproteases have been isolated from a number of procaryotic and eucaryotic sources, e.g.Bacillus subtilis (McConn et al., 1964, J. Biol. Chem. 239:3706); Bacillus megaterium; Serratia (Miyata et al., 1971, Agr. Biol. Chem. 35:460); Clostridium bifermentans (MacFarlane et al., 1992, App. Environ. Microbiol. 58:1195-1200), Legionella pneumophila (Moffat et al., 1994, Infection and Immunity 62:751-3). In particular, acidic metalloproteases have been isolated from broad-banded copperhead venoms (Johnson and Ownby, 1993, Int. J. Biochem. 25:267-278), rattlesnake venoms (Chlou et al., 1992, Biochem. Biophys. Res. Commun. 187:389-396) and articular cartilage (Treadwell et al., 1986, Arch. Biochem. Biophys. 251:715-723). Neutral metalloproteases, specifically those having optimal activity at neutral pH have, for example, been isolated from Aspergillus sojae (Sekine, 1973, Agric. Biol. Chem. 37:1945-1952). Neutral metalloproteases obtained from Aspergillus have been classified into two groups, npI and npII (Sekine, 1972, Agric. Biol. Chem. 36:207-216). So far, success in obtaining amino acid sequence information from these fungal neutral metalloproteases has been limited. An npII metalloprotease isolated from Aspergillus oryzae has been cloned based on amino acid sequence presented in the literature (Tatsumi et al., 1991, Mol. Gen. Genet. 228:97-103). However, to date, no npI fungal metalloprotease has been cloned or sequenced. Alkaline metalloproteases, for example, have been isolated from Pseudomonas aeruginosa (Baumann et al., 1993, EMBO J 12:3357-3364) and the insect pathogen Xenorhabdus luminescens (Schmidt et al., 1998, Appl. Environ. Microbiol. 54:2793-2797).
- Metalloproteases have been devided into several distinct families based primarily on activity and sturcture: 1) water nucleophile; water bound by single zinc ion ligated to two His (within the motif HEXXH) and Glu, His or Asp; 2) water nucleophile; water bound by single zinc ion ligated to His, Glu (within the motif HXXE) and His; 3) water nucleophile; water bound by single zinc ion ligated to His, Asp and His; 4) Water nucleophile; water bound by single zinc ion ligated to two His (within the motif HXXEH) and Glu and 5) water nucleophile; water bound by two zinc ions ligated by Lys, Asp, Asp, Asp, Glu.
- Examples of members of the metalloproteinase family include, but are not limited to, membrane alanyl aminopeptidase (Homo sapiens), germinal peptidyl-dipeptidase A (Homo sapiens), thimet oligopeptidase (Rattus norvegicus), oligopeptidase F (Lactococcus lactis), mycolysin (Streptomyces cacaoi), immune inhibitor A (Bacillus thuringiensis), snapalysin (Streptomyces lividans), leishmanolysin (Leishmania major), microbial collagenase (Vibrio alginolyticus), microbial collagenase, class I (Clostridium perfringens), collagenase 1 (Homo sapiens), serralysin (Serratia marcescens), fragilysin (Bacteroides fragilis), gametolysin (Chlamydomonas reinhardtii), astacin (Astacus fluviatilis), adamalysin (Crotalus adamanteus), ADAM 10 (Bos taurus), neprilysin (Homo sapiens), carboxypeptidase A (Homo sapiens), carboxypeptidase E (Bos taurus), gamma-D-glutamyl-(L)-meso-diaminopimelate peptidase I (Bacillus sphaericus), vanY D-Ala-D-Ala carboxypeptidase (Enterococcus faecium), endolysin (bacteriophage A118), pitrilysin (Escherichia coli), mitochondrial processing peptidase (Saccharomyces cerevisiae), leucyl aminopeptidase (Bos taurus), aminopeptidase I (Saccharomyces cerevisiae), membrane dipeptidase (Homo sapiens), glutamate carboxypeptidase (Pseudomonas sp.), Gly-X carboxypeptidase (Saccharomyces cerevisiae), O-sialoglycoprotein endopeptidase (Pasteurella haemolytica), beta-lytic metalloendopeptidase (Achromobacter lyticus), methionyl aminopeptidase I (Escherichia coli), X-Pro aminopeptidase (Escherichia coli), X-His dipeptidase (Escherichia coli), IgA1-specific metalloendopeptidase (Streptococcus sanguis), tentoxilysin (Clostridium tetani), leucyl aminopeptidase (Vibrio proteolyticus), aminopeptidase (Streptomyces griseus), IAP aminopeptidase (Escherichia coli), aminopeptidase T (Thermus aquaticus), hyicolysin (Staphylococcus hyicus), carboxypeptidase Taq (Thermus aquaticus), anthrax lethal factor (Bacillus anthracis), penicillolysin (Penicillium citrinum), fungalysin (Aspergillus fumigatus), lysostaphin (Staphylococcus simulans), beta-aspartyl dipeptidase (Escherichia coli), carboxypeptidase Ss1 (Sulfolobus solfataricus), FtsH endopeptidase (Escherichia coli), glutamyl aminopeptidase (Lactococcus lactis), cytophagalysin (Cytophaga sp.), metalloendopeptidase (vaccinia virus), VanX D-Ala-D-Ala dipeptidase (Enterococcus faecium), Ste24p endopeptidase (Saccharomyces cerevisiae), dipeptidyl-peptidase III (Rattus norvegicus), S2P protease (Homo sapiens), sporulation factor SpoIVFB (Bacillus subtilis), and HYBD endopeptidase (Escherichia coli).
- Metalloproteases have been found to have a number of uses. For example, there is strong evidence that a metalloprotease is involved in the in vivo proteolytic processing of the vasoconstrictor, endothelin-1. Rat metalloprotease has been found to be involved in peptide hormone processing. One important subfamily of the metalloproteases are the matrix metalloproteases.
- A number of diseases are thought to be mediated by excess or undesired metalloprotease activity or by an imbalance in the ratio of the various members of the protease family of proteins. These include: a) osteoarthritis (Woessner, et al., J. Biol.Chem. 259(6), 3633, 1984; Phadke, et al., J. Rheumatol. 10, 852, 1983), b) rheumatoid arthritis (Mullins, et al., Biochim. Biophys. Acta 695, 117, 1983; Woolley, et al., Arthritis Rheum. 20, 1231, 1977; Gravallese, et al., Arthritis Rheum. 34, 1076, 1991), c) septic arthritis (Williams, et al., Arthritis Rheum. 33, 533, 1990), d) tumor metastasis (Reich, et al., Cancer Res. 48, 3307, 1988, and Matrisian, et al., Proc. Nat'l. Acad. Sci., USA 83, 9413, 1986), e) periodontal diseases (Overall, et al., J. Periodontal Res. 22, 81, 1987), f) corneal ulceration (Burns, et al., Invest. Opthalmol. Vis. Sci. 30, 1569, 1989), g) proteinuria (Baricos, et al., Biochem. J. 254, 609, 1988), h) coronary thrombosis from atherosclerotic plaque rupture (Henney, et al., Proc. Nat'l. Acad. Sci., USA 88, 8154-8158, 1991), i) aneurysmal aortic disease (Vine, et al., Clin. Sci. 81, 233, 1991), j) birth control (Woessner, et al., Steroids 54, 491, 1989), k) dystrophobic epidermolysis bullosa (Kronberger, et al., J. Invest. Dermatol. 79, 208, 1982), and l) degenerative cartilage loss following traumatic joint injury, m) conditions leading to inflammatory responses, osteopenias mediated by MMP activity, n) tempero mandibular joint disease, o) demyelating diseases of the nervous system (Chantry, et al., J. Neurochem. 50, 688, 1988).
- Aspartic Protease
- Aspartic proteases have been divided into several distinct families based primarily on activity and structure. These include 1) water nucleophile; water bound by two Asp from monomer or dimer; all endopeptidases, from eukaryote organisms, viruses or virus-like organisms and 2) endopeptidases that are water nucleophile and are water bound by Asp and Asn.
- Most of aspartic proteases belong to the pepsin family. The pepsin family includes digestive enzymes such as pepsin and chymosin as well as lysosomal cathepsins D and processing enzymes such as renin, and certain fungal proteases (penicillopepsin, rhizopuspepsin, endothiapepsin). A second family comprises viral proteases such as the protease from the AIDS virus (HIV) also called retropepsin. Crystallographic studies have shown that these enzymes are bilobed molecules with the active site located between two homologous lobes. Each lobe contributes one aspartate residue of the catalytically active diad of aspartates. These two aspartyl residues are in close geometric proximity in the active molecule and one aspartate is ionized whereas the second one is unionized at the optimum pH range of 2-3. Retropepsins, are monomeric, i.e carry only one catalytic aspartate and then dimerization is required to form an active enzyme.
- In contrast to serine and cysteine proteases, catalysis by aspartic protease do not involve a covalent intermediate though a tetrahedral intermediate exists. The nucleophilic attack is achieved by two simultaneous proton transfer: one from a water molecule to the diad of the two carboxyl groups and a second one from the diad to the carbonyl oxygen of the substrate with the concurrent CO—NH bond cleavage. This general acid-base catalysis, which may be called a “push-pull” mechanism leads to the formation of a non covalent neutral tetrahedral intermediate.
- Examples of the aspartic protease family of proteins include, but are not limited to, pepsin A (Homo sapiens), HIV1 retropepsin (human immunodeficiency virus type 1), endopeptidase (cauliflower mosaic virus), bacilliform virus putative protease (rice tungro bacilliform virus), aspergillopepsin II (Aspergillus niger), thermopsin (Sulfolobus acidocaldarius), nodavirus endopeptidase (flock house virus), pseudomonapepsin (Pseudomonas sp. 101), signal peptidase II (Escherichia coli), polyprotein peptidase (human spumaretrovirus), copia transposon (Drosophila melanogaster), SIRE-1 peptidase (Glycine max), retrotransposon bs1 endopeptidase (Zea mays), retrotransposon peptidase (Drosophila buzzatii), Tas retrotransposon peptidase (Ascaris lumbricoides), Pao retrotransposon peptidase (Bombyx mori), putative proteinase of Skippy retrotransposon (Fusarium oxysporum), tetravirus endopeptidase (Nudaurelia capensis omega virus), presenilin 1 (Homo sapiens).
- Carboxypeptidase
- Carboxypeptidases are proteases that function in many physiological processes. These proteases remove a wide range of carboxyl-terminal amino acids, and in doing so are able to activate, inactivate, and modulate enzyme and peptide hormone activity. Many active forms of mammalian carboxypeptidases are located in lysosomes where they regulate intracellular protein processing, degradation and turnover. In plants and insects carboxypeptidases play a role in posttranslational protein modifications including mobilization of storage proteins and hormone activation.
- Carboxypeptidase activities are regulated either by endogenous protein inhibitors or by enzymatic cleavage of a segment of a propeptide to release the active carboxypeptidase. Carboxypeptidases A and B (CPA and CPB, respectively) are pancreatic zinc-containing proteolytic enzymes which catalyze the hydrolysis of the carboxyl-terminal peptide bond in polypeptide chains. When transcribed in rat brain and other nonpancreatic tissues, CPA is unable to function as a protease (Normant, E. et al. (1995) J. Biol. Chem. 270: 20543-20549). This inability to function as a protease has been attributed to the presence of tissue-specific, endogenous protein inhibitors such as tissue carboxypeptidase inhibitor (TCI) or latexin (Normant, E. et al. (1995) Proc. Natl. Acad. Sci. 92: 12225-12229; Hatanaka, Y. et al. (1994) Eur. J. Neurosci. 6: 973-982).
- Latexin and TCI are 222 and 223 amino acids in length, respectively. They contain several potential phosphorylation sites, but they do not show a membrane-specific signal peptide sequence (Normant et al., supra; Hatanaka et al., supra). TCI is a non-competitive, nearly irreversible, and potent inhibitor of CPA; it is less potent against CPB and does not act on various other proteases. TCI and latexin are both expressed and localized in the cytosol of a number of tissues including brain, lung, or digestive tract. It has been suggested that TCI or latexin may function in regulating tissue-specific, cytosolic protein degradation (Normant et al., supra).
- Eaton et al purified a novel human plasma carboxypeptidase B (designated pCPB protein) that has an apparent Mr of 60,000. The deduced amino acid sequence reveals a primary translation product of 423 amino acids that is very similar to carboxypeptidase A and B and consists of a 22-amino acid signal peptide, a 92-amino acid activation peptide, and a 309-amino acid catalytic domain. This protein shows 44 and 40% similarity to rat procarboxypeptidase B and human mast cell procarboxypeptidase. The presence of aspartic acid at position 257 of the catalytic domain suggests that this protein is a basic carboxypeptidase. When activated by trypsin, it hydrolyzes carboxypeptidase B substrates, hippuryl-Arg and hippuryl-Lys, but not carboxypeptidase A substrates, and it is inhibited by the specific carboxypeptidase B inhibitor (DL-5-guanidinoethyl)mercaptosuccinic acid. Tsai and Drayna (1992) used PCR to identify the presence of the plasma carboxypeptidase B gene in somatic hybrid cell lines which is called carboxypeptidase B2 (CPB2), also called carboxypeptidase U (CPU). It is an unstable basic carboxypeptidase that circulates in human plasma in its proenzyme form. The most likely physiologic activator of pro-CPU is the thrombin-thrombomodulin complex. Vanhoof et al. (1996) noted that pro-CPU exhibits affinity for plasminogen and can be converted to its active form through the action of thrombin and plasmin. CPB2 gene is located on human chromosome 13. To regionalize the assignment of the gene on chromosome 13, Vanhoof et al. (1996) used fluorescence in situ hybridization. They found that it is localized to 13q14.11.
- For a review of the carboxypeptidase, see Eaton et al., J. Biol. Chem. 266: 21833-21838, 1991; Tsai et al., Genomics 14: 549-550, 1992; Vanhoof et al., Genomics 38: 454-455, 1996; Pascual et al., Eur J Biochem February 15; 179(3):609-16, 1989;
- The protein of the present invention has a substantial similarity to the carboxypeptidase B as set forth above. Protease proteins, particularly members of the carboxypeptidase subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of protease proteins. The present invention advances the state of the art by providing a previously unidentified human protease proteins that have homology to members of the carboxypeptidase subfamily.
- The present invention is based in part on the identification of amino acid sequences of human protease peptides and proteins that are related to the carboxypeptidase subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate protease activity in cells and tissues that express the protease. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- FIG. 1 provides the nucleotide sequence of a cDNA molecule or transcript sequence that encodes the protease protein of the present invention. (SEQ ID NO:1) In addition, structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- FIG. 2 provides the predicted amino acid sequence of the protease of the present invention. (SEQ ID NO:2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- FIG. 3 provides genomic sequences that span the gene encoding the protease protein of the present invention. (SEQ ID NO:3) In addition structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence. As illustrated in FIG. 3, SNPs, including insertion/deletion variants (“indels”), were identified at 40 different nucleotide positions.
- The present invention is based on the sequencing of the human genome. During the sequencing and assembly of the human genome, analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a protease protein or part of a protease protein and are related to the carboxypeptidase subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized. Based on this analysis, the present invention provides amino acid sequences of human protease peptides and proteins that are related to the carboxypeptidase subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these protease peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the protease of the present invention.
- In addition to being previously unknown, the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known protease proteins of the carboxypeptidase subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene. Some of the more specific features of the peptides of the present invention, and the uses thereof, are described herein, particularly in the Background of the Invention and in the annotation provided in the Figures, and/or are known within the art for each of the known carboxypeptidase family or subfamily of protease proteins.
- Peptide Molecules
- The present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the protease family of proteins and are related to the carboxypeptidase subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3). The peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the protease peptides of the present invention, protease peptides, or peptides/proteins of the present invention.
- The present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the protease peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.
- As used herein, a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals. The peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).
- In some uses, “substantially free of cellular material” includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins. When the peptide is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.
- The language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the protease peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.
- The isolated protease peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. For example, a nucleic acid molecule encoding the protease peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell. The protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.
- Accordingly, the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). The amino acid sequence of such a protein is provided in FIG. 2. A protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.
- The present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.
- The present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids. The preferred classes of proteins that are comprised of the protease peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.
- The protease peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins. Such chimeric and fusion proteins comprise a protease peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the protease peptide. “Operatively linked” indicates that the protease peptide and the heterologous protein are fused in-frame. The heterologous protein can be fused to the N-terminus or C-terminus of the protease peptide.
- In some uses, the fusion protein does not affect the activity of the protease peptide per se. For example, the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions. Such fusion proteins, particularly poly-His fusions, can facilitate the purification of recombinant protease peptide. In certain host cells (e.g., mammalian host cells), expression and/or secretion of a protein can be increased by using a heterologous signal sequence.
- A chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al.,Current Protocols in Molecular Biology, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein). A protease peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the protease peptide.
- As mentioned above, the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides. Such variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.
- Such variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the protease peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.
- To determine the percent identity of two amino acid sequences or two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In a preferred embodiment, at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.
- The comparison of sequences and determination of percent identity and similarity between two sequences can be accomplished using a mathematical algorithm. (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data,
Part 1, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991). In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) (available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4. - The nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (J. Mol. Biol. 215:403-10 (1990)). BLAST nucleotide searches can be performed with the NBLAST program, score=100, wordlength=12 to obtain nucleotide sequences homologous to the nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score=50, wordlength=3 to obtain amino acid sequences homologous to the proteins of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (Nucleic Acids Res. 25(17):3389-3402 (1997)). When utilizing BLAST and gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used.
- Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the protease peptides of the present invention as well as being encoded by the same genetic locus as the protease peptide provided herein. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- Allelic variants of a protease peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the protease peptide as well as being encoded by the same genetic locus as the protease peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR. As used herein, two proteins (or a region of the proteins) have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous. A significantly homologous amino acid sequence, according to the present invention, will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under stringent conditions as more fully described below.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “−”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and
regions 5′ and 3′ of the ORF, may affect control/regulatory elements. - Paralogs of a protease peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the protease peptide, as being encoded by a gene from humans, and as having similar activity or function. Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain. Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.
- Orthologs of a protease peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the protease peptide as well as being encoded by a gene from another organism. Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents. Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a protease peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “−”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and
regions 5′ and 3′ of the ORF, may affect control/regulatory elements. - Non-naturally occurring variants of the protease peptides of the present invention can readily be generated using recombinant techniques. Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the protease peptide. For example, one class of substitutions are conserved amino acid substitution. Such substitutions are those that substitute a given amino acid in a protease peptide by another amino acid of like characteristics. Typically seen as conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr. Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al.,Science 247:1306-1310 (1990).
- Variant protease peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to cleave substrate, ability to participate in a signaling pathway, etc. Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions. FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions. Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.
- Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.
- Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al.,Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as protease activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al, J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).
- The present invention further provides fragments of the protease peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2. The fragments to which the invention pertains, however, are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.
- As used herein, a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a protease peptide. Such fragments can be chosen based on the ability to retain one or more of the biological activities of the protease peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen. Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length. Such fragments will typically comprise a domain or motif of the protease peptide, e.g., active site, a transmembrane domain or a substrate-binding domain. Further, possible fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures. Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.
- Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in protease peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).
- Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.
- Such modifications are well known to those of skill in the art and have been described in great detail in the scientific literature. Several particularly common modifications, glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutamic acid residues, hydroxylation and ADP-ribosylation, for instance, are described in most basic texts, such asProteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993). Many detailed reviews are available on this subject, such as by Wold, F., Posttranslational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York 1-12 (1983); Seifter et al. (Meth. Enzymol. 182: 626-646 (1990)) and Rattan et al. (Ann. N.Y. Acad. Sci. 663:48-62 (1992)).
- Accordingly, the protease peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature protease peptide is fused with another compound, such as a compound to increase the half-life of the protease peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature protease peptide, such as a leader or secretory sequence or a sequence for purification of the mature protease peptide or a pro-protein sequence.
- Protein/Peptide Uses
- The proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state). Where the protein binds or potentially binds to another protein or ligand (such as, for example, in a protease-effector protein interaction or protease-ligand interaction), the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.
- Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.
- Utility_Utility
- The potential uses of the peptides of the present invention are based primarily on the source of the protein as well as the class/action of the protein. For example, proteases isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the protease. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver. A large percentage of pharmaceutical agents are being developed that modulate the activity of protease proteins, particularly members of the carboxypeptidase subfamily (see Background of the Invention). The structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. Such uses can readily be determined using the information provided herein, that which is known in the art, and routine experimentation.
- The proteins of the present invention (including variants and fragments that may have been disclosed prior to the present invention) are useful for biological assays related to proteases that are related to members of the carboxypeptidase subfamily. Such assays involve any of the known protease functions or activities or properties useful for diagnosis and treatment of protease-related conditions that are specific for the subfamily of proteases that the one of the present invention belongs to, particularly in cells and tissues that express the protease. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver.
- The proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems. Cell-based systems can be native, i.e., cells that normally express the protease, as a biopsy or expanded in cell culture. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. In an alternate embodiment, cell-based assays involve recombinant host cells expressing the protease protein.
- The polypeptides can be used to identify compounds that modulate protease activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the protease. Both the proteases of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the protease. These compounds can be further screened against a functional protease to determine the effect of the compound on the protease activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the protease to a desired degree.
- Further, the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the protease protein and a molecule that normally interacts with the protease protein, e.g. a substrate or a component of the signal pathway that the protease protein normally interacts (for example, a protease). Such assays typically include the steps of combining the protease protein with a candidate compound under conditions that allow the protease protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the protease protein and the target, such as any of the associated effects of signal transduction such as protein cleavage, cAMP turnover, and adenylate cyclase activation, etc.
- Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al.,Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L-configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′)2, Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules (e.g., molecules obtained from combinatorial and natural product libraries).
- One candidate compound is a soluble fragment of the receptor that competes for substrate binding. Other candidate compounds include mutant proteases or appropriate fragments containing mutations that affect protease function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.
- The invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) protease activity. The assays typically involve an assay of events in the signal transduction pathway that indicate protease activity. Thus, the cleavage of a substrate, inactivation/activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the protease protein dependent signal cascade can be assayed.
- Any of the biological or biochemical functions mediated by the protease can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the protease can be assayed. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver.
- Binding and/or activating compounds can also be screened by using chimeric protease proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions. For example, a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native protease. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the protease is derived.
- The proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the protease (e.g. binding partners and/or ligands). Thus, a compound is exposed to a protease polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide. Soluble protease polypeptide is also added to the mixture. If the test compound interacts with the soluble protease polypeptide, it decreases the amount of complex formed or activity from the protease target. This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the protease. Thus, the soluble polypeptide that competes with the target protease region is designed to contain peptide sequences corresponding to the region of interest.
- To perform cell free drug screening assays, it is sometimes desirable to immobilize either the protease protein, or fragment, or its target molecule to facilitate separation of complexes from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay.
- Techniques for immobilizing proteins on matrices can be used in the drug screening assays. In one embodiment, a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix. For example, glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtiter plates, which are then combined with the cell lysates (e.g.,35S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated. Alternatively, the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of protease-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques. For example, either the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art. Alternatively, antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation. Preparations of a protease-binding protein and a candidate compound are incubated in the protease protein-presenting wells and the amount of complex trapped in the well can be quantitated. Methods for detecting such complexes, in addition to those described above for the GST-immobilized complexes, include immunodetection of complexes using antibodies reactive with the protease protein target molecule, or which are reactive with protease protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.
- Agents that modulate one of the proteases of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.
- Modulators of protease protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the protease pathway, by treating cells or tissues that express the protease. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. These methods of treatment include the steps of administering a modulator of protease activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.
- In yet another aspect of the invention, the protease proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al (1993)Cell 72:223-232; Madura et al (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al. (1993) Oncogene 8:1693-1696; and Brent W094/10300), to identify other proteins, which bind to or interact with the protease and are involved in protease activity. Such protease-binding proteins are also likely to be involved in the propagation of signals by the protease proteins or protease targets as, for example, downstream elements of a protease-mediated signaling pathway. Alternatively, such protease-binding proteins are likely to be protease inhibitors.
- The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for a protease protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor. If the “bait” and the “prey” proteins are able to interact, in vivo, forming a protease-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the protease protein.
- This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e.g., a protease-modulating agent, an antisense protease nucleic acid molecule, a protease-specific antibody, or a protease-binding partner) can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent. Alternatively, an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.
- The protease proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The method involves contacting a biological sample with a compound capable of interacting with the protease protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein. A biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.
- The peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs. Thus, the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification. Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered protease activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- In vitro techniques for detection of peptide include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent. Alternatively, the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.
- The peptides are also useful in pharmacogenomic analysis. Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. (Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. (Clin. Chem. 43(2):254-266 (1997)). The clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism. Thus, the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound. Further, the activity of drug metabolizing enzymes effects both the intensity and duration of drug action. Thus, the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype. The discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the protease protein in which one or more of the protease functions in one population is different from those in another population. The peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality. Thus, in a ligand-based treatment, polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and protease activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism. As an alternative to genotyping, specific polymorphic peptides could be identified.
- The peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. Accordingly, methods for treatment include the use of the protease protein or fragments.
- Antibodies
- The invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof. As used herein, an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins. An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.
- As used herein, an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge. The antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′)2, and Fv fragments.
- Many methods are known for generating and/or identifying antibodies to a given target peptide. Several such methods are described by Harlow, Antibodies, Cold Spring Harbor Press, (1989).
- In general, to generate antibodies, an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse. The full-length protein, an antigenic peptide fragment or a fusion protein can be used. Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.
- Antibodies are preferably prepared from regions or discrete fragments of the protease proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or protease/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.
- An antigenic fragment will typically comprise at least 8 contiguous amino acid residues. The antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues. Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).
- Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include125I, 131I, 35S or 3H.
- Antibody Uses
- The antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation. The antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells. In addition, such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver. Further, such antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.
- Further, the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function. When a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form, the antibody can be prepared against the normal protein. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.
- The antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.
- Additionally, antibodies are useful in pharmacogenomic analysis. Thus, antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities. The antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.
- The antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.
- The antibodies are also useful for inhibiting protein function, for example, blocking the binding of the protease peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function. An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity. Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.
- The invention also encompasses kits for using antibodies to detect the presence of a protein in a biological sample. The kit can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use. Such a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nucleic acid arrays and similar methods have been developed for antibody arrays.
- Nucleic Acid Molecules
- The present invention further provides isolated nucleic acid molecules that encode a protease peptide or protein of the present invention (cDNA, transcript and genomic sequence). Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the protease peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.
- As used herein, an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. However, there can be some flanking nucleotide sequences, for example up to about 5 KB, 4 KB, 3 KB, 2 KB, or 1 KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence. The important point is that the nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.
- Moreover, an “isolated” nucleic acid molecule, such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized. However, the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.
- For example, recombinant DNA molecules contained in a vector are considered isolated. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention. Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.
- Accordingly, the present invention provides nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.
- The present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.
- The present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule. In such a fashion, the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences. Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.
- In FIGS. 1 and 3, both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.
- The isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.
- As mentioned above, the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the protease peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA. In addition, the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.
- Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof. The nucleic acid, especially DNA, can be double-stranded or single-stranded. Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).
- The invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the protease proteins of the present invention that are described above. Such nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis. Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.
- The present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3. Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents. A promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.
- A fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.
- A probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.
- Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene.
- As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other. The conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found inCurrent Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. One example of stringent hybridization conditions are hybridization in 6×sodium chloride/sodium citrate (SSC) at about 45 C, followed by one or more washes in 0.2×SSC, 0.1% SDS at 50-65 C. Examples of moderate to low stringency hybridization conditions are well known in the art.
- Nucleic Acid Molecule Uses
- The nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays. The nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2. As illustrated in FIG. 3, SNPs, including insertion/deletion variants (“indels”), were identified at 40 different nucleotide positions.
- The probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.
- The nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.
- The nucleic acid molecules are also useful for constructing recombinant vectors. Such vectors include expression vectors that express a portion of, or all of, the peptide sequences. Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product. For example, an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.
- The nucleic acid molecules are also useful for expressing antigenic portions of the proteins.
- The nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR.
- The nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.
- The nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.
- The nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.
- The nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.
- The nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.
- The nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms. The nucleic acid whose level is determined can be DNA or RNA. Accordingly, probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in protease protein expression relative to normal results.
- In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detecting DNA includes Southern hybridizations and in situ hybridization.
- Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a protease protein, such as by measuring a level of a protease-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a protease gene has been mutated. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver.
- Nucleic acid expression assays are useful for drug screening to identify compounds that modulate protease nucleic acid expression.
- The invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the protease gene, particularly biological and pathological processes that are mediated by the protease in cells and tissues that express it. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver. The method typically includes assaying the ability of the compound to modulate the expression of the protease nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired protease nucleic acid expression. The assays can be performed in cell-based and cell-free systems. Cell-based assays include cells naturally expressing the protease nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.
- The assay for protease nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the protease protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.
- Thus, modulators of protease gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined. The level of expression of protease mRNA in the presence of the candidate compound is compared to the level of expression of protease mRNA in the absence of the candidate compound. The candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression. When expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression. When nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.
- The invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate protease nucleic acid expression in cells and tissues that express the protease. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.
- Alternatively, a modulator for protease nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the protease nucleic acid expression in the cells and tissues that express the protein. Experimental data as provided in FIG. 1 indicates expression in fetal brain, liver, hepatocellular carcinoma and whole liver.
- The nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the protease gene in clinical trials or in a treatment regimen. Thus, the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance. The gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.
- The nucleic acid molecules are also useful in diagnostic assays for qualitative changes in protease nucleic acid expression, and particularly in qualitative changes that lead to pathology. The nucleic acid molecules can be used to detect mutations in protease genes and gene expression products such as mRNA. The nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the protease gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the protease gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a protease protein.
- Individuals carrying mutations in the protease gene can be detected at the nucleic acid level by a variety of techniques. FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “−”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and
regions 5′ and 3′ of the ORF, may affect control/regulatory elements. As indicated by the data presented in FIG. 3, the map position was determined to be on chromosome 13 by ePCR. Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis. RNA or cDNA can be used in the same way. In some uses, detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos. 4,683,195 and 4,683,202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e.g., Landegran et al., Science 241:1077-1080 (1988); and Nakazawa et al., PNAS 91:360-364 (1994)), the latter of which can be particularly useful for detecting point mutations in the gene (see Abravaya et al., Nucleic Acids Res. 23:675-682 (1995)). This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences. - Alternatively, mutations in a protease gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.
- Further, sequence-specific ribozymes (U.S. Pat. No. 5,498,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.
- Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method. Furthermore, sequence differences between a mutant protease gene and a wild-type gene can be determined by direct DNA sequencing. A variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995)Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. Biotechnol. 38:147-159 (1993)).
- Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al.,Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl. 9:73-79 (1992)), and movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (Myers et al., Nature 313:495 (1985)). Examples of other techniques for detecting point mutations include selective oligonucleotide hybridization, selective amplification, and selective primer extension.
- The nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality. Thus, the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship). Accordingly, the nucleic acid molecules described herein can be used to assess the mutation content of the protease gene in an individual in order to select an appropriate compound or dosage regimen for treatment.
- Thus nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.
- The nucleic acid molecules are thus useful as antisense constructs to control protease gene expression in cells, tissues, and organisms. A DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of protease protein. An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into protease protein. FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “−”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and
regions 5′ and 3′ of the ORF, may affect control/regulatory elements. - Alternatively, a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of protease nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired protease nucleic acid expression. This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the protease protein, such as substrate binding.
- The nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in protease gene expression. Thus, recombinant cells, which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired protease protein to treat the individual.
- The invention also encompasses kits for detecting the presence of a protease nucleic acid in a biological sample. Experimental data as provided in FIG. 1 indicates that protease proteins of the present invention are expressed in the fetal brain, liver, hepatocellular carcinoma by a virtual northern blot. In addition, PCR-based tissue screening panel indicates expression in whole liver. For example, the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting protease nucleic acid in a biological sample; means for determining the amount of protease nucleic acid in the sample; and means for comparing the amount of protease nucleic acid in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect protease protein mRNA or DNA.
- Nucleic Acid Arrays
- The present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).
- As used herein “Arrays” or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support. In one embodiment, the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application W095/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93 : 10614-10619), all of which are incorporated herein in their entirety by reference. In other embodiments, such arrays are produced by the methods described by Brown et al., U.S. Pat. No. 5,807,522.
- The microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support. The oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length. The microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence. Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.
- In order to produce oligonucleotides to a known sequence for a microarray or detection kit, the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit. The “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence. The second oligonucleotide in the pair (mismatched by one) serves as a control. The number of oligonucleotide pairs may range from two to one million. The oligomers are synthesized at designated areas on a substrate using a light-directed chemical process. The substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.
- In another aspect, an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application W095/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference. In another aspect, a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures. An array, such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.
- In order to conduct sample analysis using a microarray or detection kit, the RNA or DNA from a biological sample is made into hybridization probes. The mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA). The aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence. The scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit. The biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations. A detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.
- Using such arrays, the present invention provides methods to identify the expression of the protease proteins/peptides of the present invention. In detail, such methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample. Such assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the protease gene of the present invention. FIG. 3 provides information on SNPs that have been identified in a gene encoding the transporter protein of the present invention. 40 SNP variants were found, including 5 indels (indicated by a “−”) and 1 SNPs in exons, of which 5 of these cause changes in the amino acid sequence (i.e., nonsynonymous SNPs). SNPs, identified at different nucleotide positions in introns and
regions 5′ and 3′ of the ORF, may affect control/regulatory elements. - Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T,An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).
- The test samples of the present invention include cells, protein or membrane extracts of cells. The test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.
- In another embodiment of the present invention, kits are provided which contain the necessary reagents to carry out the assays of the present invention.
- Specifically, the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.
- In detail, a compartmentalized kit includes any kit in which reagents are contained in separate containers. Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica. Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another. Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe. One skilled in the art will readily recognize that the previously unidentified protease gene of the present invention can be routinely identified using the sequence information disclosed herein can be readily incorporated into one of the established kit formats which are well known in the art, particularly expression arrays.
- Vectors/Host Cells
- The invention also provides vectors containing the nucleic acid molecules described herein. The term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules. When the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid. With this aspect of the invention, the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.
- A vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules. Alternatively, the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.
- The invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules. The vectors can function in prokaryotic or eukaryotic cells or in both (shuttle vectors).
- Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell. The nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription. Thus, the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector. Alternatively, a trans-acting factor may be supplied by the host cell. Finally, a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.
- The regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage λ, the lac, TRP, and TAC promoters fromE. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.
- In addition to control regions that promote transcription, expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers. Examples include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.
- In addition to containing sites for transcription initiation and control, expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation. Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals. The person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al.,Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- A variety of expression vectors can be used to express a nucleic acid molecule. Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses. Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g. cosmids and phagemids. Appropriate cloning and expression vectors for prokaryotic and eukaryotic hosts are described in Sambrook et al.,Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- The regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand. A variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.
- The nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology. Generally, the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.
- The vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques. Bacterial cells include, but are not limited to,E. coli, Streptomyces, and Salmonella typhimurium. Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.
- As described herein, it may be desirable to express the peptide as a fusion protein. Accordingly, the invention provides fusion vectors that allow for the production of the peptides. Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification. A proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety. Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enteroprotease. Typical fusion expression vectors include pGEX (Smith et al.,Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).
- Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein. (Gottesman, S.,Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990)119-128). Alternatively, the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al., Nucleic Acids Res. 20:2111-2118 (1992)).
- The nucleic acid molecules can also be expressed by expression vectors that are operative in yeast. Examples of vectors for expression in yeast e.g.,S. cerevisiae include pYepSec1 (Baldari, et al., EMBO J. 6:229-234 (1987)), pMFa (Kujan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).
- The nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g.,
Sf 9 cells) include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 170:31-39 (1989)). - In certain embodiments of the invention, the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors. Examples of mammalian expression vectors include pCDM8 (Seed, B.Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J. 6:187-195 (1987)).
- The expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules. The person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T.Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.
- The invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA. Thus, an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).
- The invention also relates to recombinant host cells containing the vectors described herein. Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.
- The recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd, ed, Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).
- Host cells can contain more than one vector. Thus, different nucleotide sequences can be introduced on different vectors of the same cell. Similarly, the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors. When more than one vector is introduced into a cell, the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.
- In the case of bacteriophage and viral vectors, these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction. Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.
- Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs. The marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.
- While the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.
- Where secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as proteases, appropriate secretion signals are incorporated into the vector. The signal sequence can be endogenous to the peptides or heterologous to these peptides.
- Where the peptide is not secreted into the medium, which is typically the case with proteases, the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like. The peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatite chromatography, lectin chromatography, or high performance liquid chromatography.
- It is also understood that depending upon the host cell in recombinant production of the peptides described herein, the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria. In addition, the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.
- Uses of Vectors and Host Cells
- The recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a protease protein or peptide that can be further purified to produce desired amounts of protease protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.
- Host cells are also useful for conducting cell-based assays involving the protease protein or protease protein fragments, such as those described above as well as other formats known in the art. Thus, a recombinant host cell expressing a native protease protein is useful for assaying compounds that stimulate or inhibit protease protein function.
- Host cells are also useful for identifying protease protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant protease protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native protease protein.
- Genetically engineered host cells can be further used to produce non-human transgenic animals. A transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a protease protein and identifying and evaluating modulators of protease protein activity. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.
- A transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. Any of the protease protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.
- Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the protease protein to particular cells.
- Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B.,Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes. A transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.
- In another embodiment, transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P1. For a description of the cre/loxP recombinase system, see, e.g., Lakso et alPNAS 89:6232-6236 (1992). Another example of a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991). If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein is required. Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.
- Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al.Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e.g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter Go phase. The quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal. The offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.
- Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, protease protein activity/activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo protease protein function, including substrate interaction, the effect of specific mutant protease proteins on protease protein function and substrate interaction, and the effect of chimeric protease proteins. It is also possible to assess the effect of null mutations, that is mutations that substantially or completely eliminate one or more protease protein functions.
- All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.
-
1 4 1 1625 DNA Human 1 gaaaattgct gttgggatga agctttgcag ccttgcagtc cttgtaccca ttgttctctt 60 ctgtgagcag catgtcttcg cgtttcagag tggccaagtt ctagctgctc ttcctagaac 120 ctctaggcaa gttcaagttc tacagaatct tactacaaca tatgagattg ttctctggca 180 gccggtaaca gctgacctta ttgtgaagaa aaaacaagtc catttttttg taaatgcatc 240 tgatgtcgac aatgtgaaag cccatttaaa tgtgagcgga attccatgca gtgtcttgct 300 ggcagatgtg gaagatctta ttcaacagca gatttccaac gacacagtca gcccccgagc 360 ctccgcatcg tactatgaac agtatcactc actaaatgaa atctattctt ggatagaatt 420 tataactgag aggcatcctg atatgcttac aaaaatccac attggatcct catttgagaa 480 gtacccactc tatgttttaa aggtttctgg aaaagaacaa gcagccaaaa atgccatatg 540 gattgactgt ggaatccatg ccagagaatg gatctctcct gctttctgct tgtggttcat 600 aggccataat cgaatgtgga gaaagaaccg ttctttctat gcgaacaatc attgcatcgg 660 aacagacctg aataggaact ttgcttccaa acactggtgt gaggaaggtg catccagttc 720 ctcatgctcg gaaacctact gtggacttta tcctgagtca gaaccagaag tgaaggcagt 780 ggctagtttc ttgagaagaa atatcaacca gattaaagca tacatcagca tgcattcata 840 ctcccagcat atagtgtttc catattccta tacacgaagt aaaagcaaag accatgagga 900 actgtctcta gtagccagtg aagcagttcg tgctattgag aaaattagta aaaataccag 960 gtatacacat ggccatggct cagaaacctt atacctagct cctggaggtg gggacgattg 1020 gatctatgat ttgggcatca aatattcgtt tacaattgaa cttcgagata cgggcacata 1080 cggattcttg ctgccggagc gttacatcaa acccacctgt agagaagctt ttgccgctgt 1140 ctctaaaata gcttggcatg tcattaggaa tgtttaatgc ccctgatttt atcattctgc 1200 ttccgtattt taatttactg attccagcaa gaccaaatca ttgtatcaga ttatttttaa 1260 gttttatccg tagttttgat aaaagatttt cctattcctt ggttctgtca gagaacctaa 1320 taagtgctac tttgccatta aggcagacta gggttcatgt ctttttaccc tttaaaaaaa 1380 attgtaaaag tctagttacc tactttttct ttgattttcg acgtttgact agccatctca 1440 agcaagtttc gacgtttgac tagccatctc aagcaagttt aatcaatgat catctcacgc 1500 tgatcattgg atcctactca acaaaaggaa gggtggtcag aagtacatta aagatttctg 1560 ctccaaattt tcaataaatt tctgcttgtg cctttaaaaa aaaaaataaa aaaaaaaaaa 1620 tacat 1625 2 386 PRT Human 2 Met Lys Leu Cys Ser Leu Ala Val Leu Val Pro Ile Val Leu Phe Cys 1 5 10 15 Glu Gln His Val Phe Ala Phe Gln Ser Gly Gln Val Leu Ala Ala Leu 20 25 30 Pro Arg Thr Ser Arg Gln Val Gln Val Leu Gln Asn Leu Thr Thr Thr 35 40 45 Tyr Glu Ile Val Leu Trp Gln Pro Val Thr Ala Asp Leu Ile Val Lys 50 55 60 Lys Lys Gln Val His Phe Phe Val Asn Ala Ser Asp Val Asp Asn Val 65 70 75 80 Lys Ala His Leu Asn Val Ser Gly Ile Pro Cys Ser Val Leu Leu Ala 85 90 95 Asp Val Glu Asp Leu Ile Gln Gln Gln Ile Ser Asn Asp Thr Val Ser 100 105 110 Pro Arg Ala Ser Ala Ser Tyr Tyr Glu Gln Tyr His Ser Leu Asn Glu 115 120 125 Ile Tyr Ser Trp Ile Glu Phe Ile Thr Glu Arg His Pro Asp Met Leu 130 135 140 Thr Lys Ile His Ile Gly Ser Ser Phe Glu Lys Tyr Pro Leu Tyr Val 145 150 155 160 Leu Lys Val Ser Gly Lys Glu Gln Ala Ala Lys Asn Ala Ile Trp Ile 165 170 175 Asp Cys Gly Ile His Ala Arg Glu Trp Ile Ser Pro Ala Phe Cys Leu 180 185 190 Trp Phe Ile Gly His Asn Arg Met Trp Arg Lys Asn Arg Ser Phe Tyr 195 200 205 Ala Asn Asn His Cys Ile Gly Thr Asp Leu Asn Arg Asn Phe Ala Ser 210 215 220 Lys His Trp Cys Glu Glu Gly Ala Ser Ser Ser Ser Cys Ser Glu Thr 225 230 235 240 Tyr Cys Gly Leu Tyr Pro Glu Ser Glu Pro Glu Val Lys Ala Val Ala 245 250 255 Ser Phe Leu Arg Arg Asn Ile Asn Gln Ile Lys Ala Tyr Ile Ser Met 260 265 270 His Ser Tyr Ser Gln His Ile Val Phe Pro Tyr Ser Tyr Thr Arg Ser 275 280 285 Lys Ser Lys Asp His Glu Glu Leu Ser Leu Val Ala Ser Glu Ala Val 290 295 300 Arg Ala Ile Glu Lys Ile Ser Lys Asn Thr Arg Tyr Thr His Gly His 305 310 315 320 Gly Ser Glu Thr Leu Tyr Leu Ala Pro Gly Gly Gly Asp Asp Trp Ile 325 330 335 Tyr Asp Leu Gly Ile Lys Tyr Ser Phe Thr Ile Glu Leu Arg Asp Thr 340 345 350 Gly Thr Tyr Gly Phe Leu Leu Pro Glu Arg Tyr Ile Lys Pro Thr Cys 355 360 365 Arg Glu Ala Phe Ala Ala Val Ser Lys Ile Ala Trp His Val Ile Arg 370 375 380 Asn Val 385 3 55827 DNA Human 3 tcgaatatta cattcagcta aactagtact tgaaagtgaa ggcaaaagaa agttattgtt 60 aaagatacag agcataaaag attttatcac ctgtagactt ttgctatagg aacttttaaa 120 agattgcttc agcaataaga aatgtaattt aaaatttatt gttttttatg cactctgttt 180 cttttgtatc ctgtttctgt ttccccagag aggaaacagg acataaaata aagaagaaac 240 acagatacaa aataagtagc acaaaaattg atagaattta ttagcatatt ttaactattt 300 tgactgttta ttttaaagtt aacttttatg ttaaaaagat aaggtaaaag ttacttgggt 360 tagtttttct ttctctcctt cagtgtgatt atgttattca tttgaaacac aggttcgttt 420 ttgtttgtat tattttttaa aatttatttg tttgcttgtt ttaagtacat atgtgaaaag 480 aacatggttc taaaattcag agtagttcta aagttcagaa ctattcaaaa cacttcaccc 540 aaagaagcgt ccctccctgt ctcttctacc ctgtcttttc cagtgtgttt ccactcacct 600 cccgtggata accagtctca ttgatttcta atctatcctt cttatgtttc tttctccaca 660 tatgagcaga cacacacata ttttcttatt tcttcttctt tcttatacaa caagtggtta 720 cagtggaggt cactttaatt cattaaatat cattcaatag ttttaaatct caaaaggaaa 780 agtttgaaat ctcaatcatt ttcttctggc caggcacgat ggctcacgcc tgtattccca 840 gcactttgga aggcagaggc aggtggatct cctgagctca ggagtttgag accatccagg 900 gcaacatggt gcaaccctgt ctctactaaa aatacaaaaa aaattaaccg ggtgtggtgg 960 ggcacacctc tagtcccagc tacttgggag gctgaggcag gagaattgct tgagccccag 1020 aggtgaaggt tgcagtgagc caagatcacg cctctgcact ccagcttggg ctacagagtg 1080 agactctgtc tcaaaaaaaa aaaaaaaaga aaagaaaaaa gaaaaaaaat cattttcttc 1140 tcagaagtta attgtgggca ggctgattta ttttgcaaat ttgccaattc tgacttcaag 1200 aacattcaag tgcattaacc aatgggaatg taggggaaga gggctccact cacttacaga 1260 gggtaggata tggcctcata ctagacaaaa tgttatttga tgctactttc aagatgatag 1320 gggatgggcc tggatttaat tgatggctat tatggtgacc tttaaataaa tgagattcaa 1380 agtaacctga tgtctttact gcttgaacca gcttccatga aatagtattc ctattggggg 1440 tgggcctatc attccatatg gtcaaggaaa catctttttg aacagagatc ctgtaatcat 1500 ccttacaaac tgcacttcaa cattggattg gattagccag atttgaggaa ctcacttttt 1560 acgtcttcat aaatttaaaa tgttgaaaaa gtcagaggca agggaagaca tttatagtac 1620 ttcacggtag atctccctca acatgggcta tatatccatt agtcaatatt ctatagctat 1680 tgttctgcaa taaaccagac aagatcctac tgtattacta cccttttatt cttggcccta 1740 ccttccccaa ggagttacac attttctaga tagtctaaat taagagcaac tctcatcata 1800 ctctttttga gtgtttaatt atcaagcaac agcctaacta agccaataat atttctcttt 1860 ttgggagtgg aaatggaagc taagttgatt gacccacagg aacaagaggg aacatgccgt 1920 tatattttaa ccagtgtgta aagaaggctg ttatgcaatc aatgatctgg gtttttctct 1980 tcagagaaat ttgttgtaca gaaaattgct gttgggatga agctttgcag ccttgcagtc 2040 cttgtaccca ttgttctctt ctgtgagcag catgtcttcg cgtttcagag gtaacccaat 2100 agaatcttag actgtggtgg gccactctcc tcacttgttt gcctcatgtc gtgtcaagtc 2160 agtgcactga gctggtggac aaaatggtaa actttgaagg ccaggtcttt cagaactttc 2220 caagttgccc tgacaaataa gtagacttta gcacaatggg ctatcactaa agacagggtc 2280 ttttttcttt cctggctctg gttttattat tgggagaacc ttggatgata cgcatatcca 2340 gtgactatgg agattcaaga aattaaatct tttataaacg taactattta tactctaact 2400 tgatgtatga ttcatattct tcctgtcttc acataaaaaa agttaactat ggatcattta 2460 ttttcccctt gtacatggaa cataggagga agaagagggt gaagtgttaa ataggaggtt 2520 tggatcatgc atgattattt agcatggaat atgaaaggaa gaagagttgt gtgataaaga 2580 actattatct gattcttatt ttgcttagta gattccctta ggataaacta tctagaagaa 2640 cacaaatgaa ttcatgctat agcacatgca atgcatggag aaaatagttc cagggtatat 2700 gtaatgtaat ttattaagta gtcaattttt aggctttaaa acattgatat tgtttccttt 2760 ggaattatct tattttttcc cctttgtttt ggttctatga tcgctttctc ctccaattat 2820 ctttgagaca gatccctctc ctcatgttag taaatgacaa agaaagaaga gacatagggc 2880 aaaggaatat accagtgaca aggaacattc taccaccaaa aaaatgttca cggtcataaa 2940 taaccatagg acaatggttt ggaaaataga tcttgacttg tgagcctgaa gctgtgtttg 3000 tacatgatca ctgaactgat tatagttgat tgatcttctt ttgttcaaca tgattgtcga 3060 atgtcgagca acaaattcta tcataaaatg atattatttt tgttatttaa ttgacgtggg 3120 ggtcaagatt gctgcaatga tcagtgactt atgtctttct ctgtatttta tcggtgaatc 3180 atatggtcag gatttctaag gttcttgcta gttctaatat tccataactt gataattggc 3240 ttcagttaag ggaaaggggg agaagagaaa aattggtatc aacatgtcca acttggctac 3300 tgtacacagt ggcagtacca ttgacagtta ggggaaaggg aggaaacctc tgcttattta 3360 gtgcctgtgt ttgtgccagg cactgaacta gtcacttaga aatgttatct ctttaaatgc 3420 ataaaatcct acatgctagg aatctttact gacattttac aaaggaggaa actgagcctc 3480 aggaagaata aataattggc ccaagatcaa acagtaaatg tagagcttgg attcaaaccc 3540 actttagcct catttcaact ccatgcactg gacagcattg cctccataaa atctggaaat 3600 taggaagaga gccagtttga aggaaggtca gatttagtca aagggagttg caggcagcag 3660 ttggtttgga aagtagcttg gaagagaggt tcgggattag aggttcagtc tcatggttct 3720 cacccactag cagatctaat catggccttg gcgtcagccc agtgcaatta tcctcagctg 3780 gttgttgcag aggttggcgg gcaggtgggc tcactgcaga ccgccatctt gatcgtagag 3840 taacccaaac tcttggatag gataatcaat agcaaaacac actaaaagct ttagcacatc 3900 tcttcaaatg agtacgtgta tagcagctta gtgacactaa atataacgca aatagaagaa 3960 gtagccaaca ataaaatagt aaaaaaatga gtgagaacat atcttcatgc atgggctttg 4020 ttactatttg ttgcttcagc ttatactctg aaatctgact gatacttatg cttgaaaaaa 4080 ggaatgagaa tgtgactata ttttaaccaa agaatatcac attaaaaata tttaatactt 4140 ttgcatactg cgagggtccc tttgcagagg agaggaggta ggaggacctc agtattgtag 4200 acagatgaat atctgaatcc tggttcccat cccttcactg gaaataacat tgcaaactac 4260 tctttctgtg agtaaaaata aattttttta ccaaatgttt ctgtgctcca cttttccagg 4320 aatggcctat tcctgaagct aaaaaggaaa tctaatttca ttcagggcaa cagactttga 4380 taaattgttg ctggggttca gaatatcaac ccttctaaaa aaaaaaaaaa aaaactaaca 4440 gtctggcttt ttcttaaagc tgttctttgt tttttttttt ttttttttgt cataatcatt 4500 ttcctactaa cagtttttat tcatgcagtc tcttagtggc tgatttgtag gttcattttg 4560 ataaatttca tcagtgaaat gccctggaac aacaacaagt tttaaaggca taaatatcat 4620 atgccaaagg gaaaggcagc caaaaaatca tgactccata ttcatttgct tttaaaagcc 4680 aaacactata aagggtaaaa ataaaatact agcaagaatc ttgtaaacag aatcagtaat 4740 tgtattgtgc agtgattacc taaatgcagc ctgccagccc agactatttg gaaagaggaa 4800 gtaagagaca ctaggaagaa gacttaggaa ttagagagtg gaggagggtt gaggataaag 4860 ggcttctgaa ttattaatag accacaggaa gtgttcctct gttgacttca catactgttt 4920 gggtacctgg agaccagttt actctctttc actttgttcc tactgatgta ttgttttcat 4980 ctcaaagaac aggccaccag tggccttaaa acactgtaat gtgtgcaaca aaattgcagc 5040 cttgggctat gttccattgt tcagagacat cttgccagct ttttaaattc aaaataatct 5100 ttcagaatgg tgaaagtgtg aaccctcccc tgtaaaccat agcaggggat acaccccaat 5160 gaacataatg acattctcag aagggaagga acagaggaag tgttgcatag gtattaaaag 5220 ctcaggatct ggattcgagc cccagatctg ctacttatca cccatgcaga cttgggcaat 5280 ttgctcgtcc cctttcagcc tttacttttt ttgtaaagtg acctgttact tcactgtgct 5340 tgtacttctc attcgatttt tggtgcaagg ctgttctttt ttctcaagtg gttattgtgt 5400 aagtgctata atcgtatcat tcagagacgc agttgaaaca cagctttagt ttttgtctcc 5460 cattgcccca tgacattttg cgtagtgggg ttatctatca ctgctctcgc atggaaagtt 5520 agaaaatttc aaggcttttt agcctgcttt taagtgacag tccttgggtc ctgctaaaaa 5580 tacaaatagc ctcaatttag aaattagaat gtcacctcca accaaggtat tgttcaaata 5640 tccccatctt tgttgttaaa agaaaatctt taaaagaatt atatttagca aaatttaatt 5700 gaacaaagaa caattttcta atcaagtaac cctcaaaaac gaaagaagtt cagagagttc 5760 tgctcagcaa agtgggcagg cagcacttat aaacagcaaa tggaaatgag gtccagaagc 5820 agcttgagta gttacaggtg agcagttgtc ttactgggca taggctgatc agttggccac 5880 atgggattgg ctgtagcttg gctgctgtga ttggctgaga ctcacctcgt tagtacaaaa 5940 aaaaaatact cctaagttag gttgcagttt gttatgtagc gactcaagtt acgaggcatc 6000 ctcagaccaa atttagttta atttaacatt atttatagga aaacaactgc ctcacctctt 6060 ccacaaacac accttactct ttttcttgtt agtctttttc tcgagttcta acttcttaga 6120 gttgtgtgag acatctttat tggggaagcc tctggaccag gacagatgct tctttgtcta 6180 ggttttcact tgcgactcca tccttccccg ctaagagtct tgcttctacc tctgggctct 6240 tgttgttgag aactttccat ccctttaggt ggccctattg gatggcatct aacattaagt 6300 gtttcttttc attttaacta ctactatcta gccaactaga gaccagccac atgcaggttt 6360 agctttatca ggagaagcca ggcaccagtc tttgtgtctg taaatttgag gaaacatcca 6420 actctctcat tatctcctgg aagtccccct actaggctga ggtaagggga gtgcaccccg 6480 aaacttcatc cctttgggag ggtggtgact tacagaacca taaaaacatg ctaaaaaaaa 6540 aattcacaaa tcctctccct ctttccactc tgacagcttt ttatatagcc tgtttatgac 6600 taagtaaggg gaagcagtca tgaaaccagt ttccaaaaat agagtgatct gactgaccct 6660 catcccatta cctaactctg ttgtgttagc actttgctca aattctgcat aagaagagtc 6720 tgttcactac aagctgaact tggacatatc aataaatttt tggtgaattt ttaacttcat 6780 aattttactc actatttcct aacttatttt ttgaatttcc tttatttttt cttcttaaga 6840 ggtctcattt ggataacata catttttacc tttatatttt ctttctttct ctgcttgttg 6900 actaattttt atacttttct ccttctttaa tacattaggt ttttttttaa tttaatactg 6960 cccactcaac attttttgtt cattattttc tttctttctt ttgagaccta gtcatgctct 7020 cttacccagg ctggagtcca gtggtgtgat tttggctcac tgtaacctcc acctcgtggg 7080 ttcaagtgat tctcgtgctt cagccttctg agtagctggg actacaggtg tgagctacta 7140 tgccacgctt atttttgtat ttttagtaaa gacagggttt caccatgttg gtcaggctgg 7200 tcttgaactc ctgacctcag gtgatccacc cacctcggcc tcccaaagtg ctgggattac 7260 aggcgtgagc cactgtgcct ggcccattat tttcaatata atagattatc taccatactg 7320 ccttgtgagg attaaataag aatacctgta aagcacttag cacaatatcc aagttactaa 7380 atatcagtaa aaaagaagaa aagtcccccc agacatatta tgctctagtc aacacaagac 7440 ttcctctaca tggacttgaa attcagcatc tctttagata atgaagagct cattgcttga 7500 taaggtgtcc tatctcatgg ttagctcaaa ttgttagaag ttcacactga aattacagtg 7560 atttaatgat atgaacctcc acttctctat actttacatg aaaaggaagc tttgagtttg 7620 ccacatcttt tgctacaact cccaaaatca tgcccaacca acttttaagt aagggccaca 7680 atcttgaccc cagcatttaa gacccttaac aatcaggtcc taccctgcca ttcgtcctgg 7740 ctttatttcc tggtatatct ctatataggc cccatatttc tgcccagctg gatcacttct 7800 ccttccttga gctctgattt tacttttcta cttgtgcacc tgcatttatg atgtttcatc 7860 tccaattcgt ttagcaaaat tctgcctatg ttagtcttat accatctcat cttcccttca 7920 cctattgaat cctagtatct cagaagtcca actcagaata tctccattct ctgactacgt 7980 aagtcaaaaa tgatacctga ctttgtattc ctgtagcaga atatttatac cactcgcatt 8040 gtacttttag tgttttatct cacagaatag gcatttgtat cagttgcagg ttagtttccc 8100 caggaaacag actcctgaga tgaagattgc atggaggaag tttactggaa aggaatctca 8160 ggatcagcat ctgtggagga atgaaggaag aaggcttggg cagaggagaa actgacctgt 8220 gatgtaatca caactatggc ctcacctgtt cctgtggaga gccttgaggc tgggttggcc 8280 tggtaaagtt gtcccaaact ggggcaagca ggcatgcctt tgtaacccct gtttattagt 8340 cactgggtgt ggattgtacc ttggaggagg catcatgttg ggcagcacag ctctcttcag 8400 gcaagggcaa gtcctagaaa gggactcagg tgagaatatc agctgccaac cctcccagaa 8460 gctgaggaga caaagaagct gaggaaataa gagttcatcc ctggatggag atctaggcag 8520 caaaacgtga catctactac agtccaaccc tttgtgtcac tcaggtcaat tttcttcata 8580 aaataagctt tgagatcaac tcttctgggg ttttgcttgg tccctcttcc taaaggaaat 8640 atacaagagg aacgttagtg aaataaacta caaccttcac agctacagct agtctcgagg 8700 ccataaccaa tacttgtcat tcctcttctc ccctacccgt tctgttttcc ccaaagaggt 8760 gccctttgct agcacctctt ctaatctagg tggtttacct ggtgagacaa cccagaccct 8820 caatcctcaa ggatctgagt cataatcact gggccctctt gggccatggc tgctgcaatt 8880 gtctgtatac atcaaatttg gacaagggaa tattacagaa cgcctaagct ggattccaaa 8940 catattcttc cctgccacat tcagtatgta agtgcagccc tcaatgtcct tctgattatt 9000 ggagtcaatt acccttcctg catggctaga aaacccatgg taactcctcg ccttcctgat 9060 aatcaatcag catgaggaaa ctgaaatgac tggacagtaa caacagcttt cagtttaaag 9120 gaactcttcc tatgctctct ggaaaccgga atttttataa gtacagagtc catatttgta 9180 gatttaaagt actaattctc cgagtgggtt acttggagtg acggtatatg gaaacactcc 9240 aacttggttc ctggaaccat gtatactacc tagtagggac acagcaccac atgagtattg 9300 atttaaagtg tgcactggag gatgttgcct tccaagttag cacctcaatt gatccttcaa 9360 caaaccattt ttatttcagt aacaggatag cagcaactag gtattctggt atgtgagagg 9420 ctaagtggat tccatggtaa tggacccatt tctgcaattc ccttgttgta aagtggagcc 9480 catgatctga taggatgtta tgtgagatgt tttatcagtg gtcaaacact ccgtaagccc 9540 ttgtatggtg atgcttgcct gaggccctac aggcaggcga gataaaccca tacccagagt 9600 ggaagaggac agatgtagtc aacttaccac ccagtgacta gctggtctct atgaggaatg 9660 gtgctgattc cggggctcaa ctttggtctc cgttgctggc aagttagaca tggggcagca 9720 acagtagcta gatcagcctt aatgagagga gtccgtgctg ctggagccat gcacacttca 9780 tctctgccat caggctattc tgttctagtg ccttttgtgc cagcattggg gtggctgttg 9840 acacaggctg actgacatca actggctgag tcatttgttt atgcagctgt ttaatgtcta 9900 ttctgttgtg ggtgctcctg gttaggcatt aataaatgat acaaagatct tcacactttc 9960 tgcccactct catagttcca ttcacatccc cctttctcca atctctttgt ctccaatctg 10020 tcaagatttc ttcttccagg ttcttgaggg gttttccagt catgtcactt gccactctcc 10080 atgaattcct gcatattcta acactggaaa caccttttcc acccaaggtg tatgatgaga 10140 tgcaacactg aagctctgcc tatttgggac gatttccctc tctgctctct ttcggtcacc 10200 cgagtgagtc cataatgcag caccacttca cttttttttt tcttttttga gatggagtct 10260 ccctctgtcg cccaggctag agtgcagtgg tgcgatatta gctcactaca acctctgcct 10320 cctgggttca agcaattctc ctgcctcagc ctcccaagta gctggcatta caggtgcccg 10380 ccaccatgcc cagctaattt tttgtatttt tagtagagat gggatttcac catattggcc 10440 aggctcgtct cgaactcctg acctcaggtg atccacccac ctcggcctcc caaagtgctg 10500 ggattacaag cgtgagccac cgtgcccagc ccacttcatt ttttacttgt acccatgcac 10560 tatcaacttg actgtccatg tatcagactt cctcttccta cttgtgtcag ttatgatcct 10620 ctgagaagca gacaccaaga tgggattagc tgtgcaagag gtgtgttgag gaaaatgctt 10680 gggtgcaaga aatggggaga gggctggagg aggctgggag agccatgaga ctgcaatgca 10740 agcttaaccc ctgtggagga gagaggaaag gaaggaagca ggtagggaac atttcaggtc 10800 gtagtgcagt tctaagaaag ttttggcaaa accaaccaag agtcctggcc aggcacggtg 10860 gctcacacct gtaatcccag cactttgaga ggccgaggtg tgtggattac ctgaggtcag 10920 gagttcgaga ccagccttac caatatggtg aatccccgtt tttactaaaa atacaaaaat 10980 tagccaggtg tggtggtgcg tgcctgtaat cccagttact cgagaggctg aggcaggaga 11040 atcacttgaa cccacgaggc agaattgtag tgagccaaga ttgctccatt gcactccagc 11100 ctgggtgaca agagcaaaac tctgtctcaa aaaaaaaaaa aaaaaaaaaa agtcctatag 11160 gcagagtcac acatcagaag agtttccagt tttgtagaaa gagcctccct tagtatcccc 11220 accatactca gttattagct gcaagaagcc agtgggaaat gtggtattag cactaacaca 11280 gggacagatt tcagagcaca gtagctgggg gcttatatca agtacacatc ttgcagctgg 11340 agagtgagaa agttaattaa agctgaggca agactgtaaa tatgcactgg tgtctgtccc 11400 aagtggatgt taactgttct gatgcttttt ccgactgaca tatccagcgc aatagctgaa 11460 taccatatgc ctgagactct accccggcaa agatgccaca tcaagcacta tggctgcaat 11520 tgagattgtt gcttggttga gtttgattgt ttgctgtcgt tttccaggat ccatctggtt 11580 tttgtgggat ccagatggca aattaaatgt ggttttgatg ggatctatca tccctgcatc 11640 ttttaggtct ttaagggtgg tactgatatt tgtcatttcc cctcaaggat gaattttttt 11700 tttttaattt tgatatcttg gctgggaggt tgggcaattt cagaggtttc cttttggctt 11760 ttcccactat gatagctctg gtcttacagt caaggaaaca atgtggaggt tctgccaact 11820 acctagtatg ttcatgtcaa ttatacattt ggtgaccagg gaaataatga tgggggaatc 11880 cattaacatg gtgcacccgc tatgagctag tcttaggcta gggctccaga tacccaagtt 11940 tcaaaatcaa cttggatagt gaccctgcat ccaacacacc tgaaaatatt tgagtattac 12000 cctttcccca gggtgcagac ttacctgagg aaatttccat aggtctcttt gggaaaggac 12060 tgaaggagtc atgatctttt tagattcttt ttttatacag ttgcagggtc tttccttgtg 12120 gggacctgac tcctccttca ggcaagaaat tctgggtcta agaacagctc agatctggaa 12180 aagggcaatg gattatgact tttgattagg atagctgtcc tcagcctctc tcattatcca 12240 gctttgattt atttttattg taaagattga gcaatccttt tgttggctgc ttctctatct 12300 tgcccctaag aactctgtgt tctcctaacc gactccacaa ttttctaagg gtcatggtcc 12360 tctggctgcc actccgacct tactgctcat tgtaataact gtgcccaact tgttactggt 12420 ggttaagccc tcccgcctgg cttctctata cagggatctt aacatctcca ttggtatcag 12480 agagctcagt tctgtaatgg catgtcctgt agttagccct caggatctat tcccacctcc 12540 cctcctggcc ttcaagccaa taacctaggg tagtcacaac ataagctggc tgtggaagtg 12600 ctgggcatgt taacaaagga aagggactat accccaaagg aggtgcactc acccatgcta 12660 cagaatttaa cattctagtt agttccttga gaggtggtac aaacatgctg ttagggtagt 12720 ttttggaagc ttggagaaag catggcctgc accatctgag ctagaaatgt cagagcgaat 12780 gtggcagatg gtgaaaaaag agatagagca cactagaata aaaatgctat gtaaggctag 12840 aaaacccact gggtgactat gctactccaa gggcccagag aacattctgt ttatgaaaat 12900 aataaggaat gtgctggtga gatgagaggg ttaccagcat cactgagaag cttgttagtg 12960 gctttttcac agtcaaagga gatttttctt taaatttaat tttcttgaat aaatacaaga 13020 ataggagttc ttttgggttt aaaaagtaaa caatacagaa aagcataaaa ttagggagaa 13080 aatactaaaa tttcaccatc ctggtgaaaa tatgaacatg tttgtgatca tcctttcata 13140 catttctcca catagttata cctccctggg tataattgta tactagttca atgttgtatc 13200 tcctattggt actatagaaa cctttctttt aaaaagaatc tcatttgttc ttcccctgcc 13260 acttacccaa ggcttcaatt gccatttccc accctccaaa tcaaagctaa caatgtgttg 13320 tttatttatg tataattttc tcctgatttt aacacatata atttttcttt atctttctaa 13380 cttttttcca aaaataggat catatttcat aaagttctcc atatcttgct tttctccctt 13440 aatatgccat ttaaagcccc caagttaact gttataaatc aaactcattt tttataatga 13500 ctgaaaagca ttctagaatg tggagacact accaacattc gacaattctg ttactgctga 13560 gcattcacat ggtttttagg ttttgttact atgaataatg ccgtaataca catccttgaa 13620 catgtatctt taatcagtgg tttaatagtt tatgctaaac ttgtaccaga gattgacata 13680 aaatttctca gtctagctac ttttcccctc ttctaataag caagtctctc catagactta 13740 tttccagaat tcagaatatt ttactcagga tttccaaaat aaagccaccc tccacccttg 13800 ttaaagttat ccttggtggg cgcggtggct cacgcctgta atcccagcat tttgggaggc 13860 tgaggcgggt ggattgtctg aggtcaggag ttcaagacca gcctgaccaa catggtgaaa 13920 ccccatctct actaaaaata caaaaattag ccgggcatgg tggtgcacgc ctgtaatccc 13980 agctactcag gaggctaagg caggagaatc gcttgaaccc agaaggtgga ggttgcagtg 14040 agccaagatc acgccattgc actccagcct gggtgacaga gcgagactcc atctcaaaaa 14100 caaacaaaca aacaaaaaca aacaaaggaa aacaaataaa attatcccta taaatcacag 14160 ctcaaatgtt acctttctaa cttctaattg cctacaagat aaagtccaaa tttctcagca 14220 tgcattcaag accttctcta gggaaggatg aacataactt cccacactca tttctgttta 14280 gctcccattc ttctcttgct ttaaacaccc gtatcctata cttggcaaca atgaacaaga 14340 gccatttttc caaaaatgcc ctttatctct tgctattgtg cctttaccca ctcttagaca 14400 ttcttacaca cccagacatc ccttctatga agcctttgct aataatgaca aacagaagtt 14460 atcataacct cttttgtgct ttgagagctc ttggtacatg gttttcttaa ataagatgat 14520 ttatttggaa tatttttaga tttacagaaa agttgccaat tgtaatacaa ctgtataccc 14580 ctcacccaat ataccctaat gttaacattt tatattatca tgatgtatta gtaaaaactg 14640 agaaatcaac attgttatat tactattaac taaactccag acttttttgg atttcaccag 14700 ttttcccact aaagctcttt ttctgttccg agatctaatc cagaacacca tgttgcattt 14760 agtcataatg ttgctgttgt ctaatgtctt gagtgctgtt gttccataca ttttgtccag 14820 gtttttagtt atttcataaa ggagggtata actggaagca aagtctaaga ttagttttaa 14880 ataaagcaag aggaagcatt ttttctaatt taaaatatat ctatcgtcat atttcaaggg 14940 caatatttgt ttgaaaataa aagaaaaatc tcgttcagtt aaaaaaaagg gggggctcag 15000 agctggcaaa tgccaccaac atgcttaatt ttaatttaaa taaaatagtt cttgtgaggt 15060 tactcagtgg tatactggaa acctgagaat gccattgccg ttaacagagt ccacaatccc 15120 tcacctcact gcttcctttc tctccttatc acttacctat aaaactggat ggagagctgc 15180 agaaatgagg acatttgcta agaaattctt tcttttctaa gtggtatgtg aaaataaagt 15240 aaattcatgt tgagtcacat taatctattg ccttggctgt gtaagaatca ccaagaattc 15300 tcacaacctt agcaacagtt gcaaaataga aatacaacaa agcaaaggtg agaaaaccaa 15360 ccaagtgtct gctttttaaa caatctattg atataattca ccacattaag atattaagcc 15420 agaaaaccca tatgctcatc ttatagaaag catttaaaat ccacacttat tcatcataaa 15480 aactcttaac aaagagcaag gagtttttta aaactgataa aagacatcta ccaaaaatct 15540 acaacaagca ttctaatggt aaaatatttt aaggtttttc ttaaaaatca ggaatcatgc 15600 attttatctc cacttctatt caatgttgta ctgaagtccc aggcaacaca gcaagacaaa 15660 aaggaagggg aaaaggggct ctataagcat tgaaattaaa gaagcagaac gtattaaaag 15720 tacattaagt acattaaaag taacggcaaa aaccgcaatt acttttgcac caacctaata 15780 gtgtgtgcag atgtaatgat tacttgcaaa gagaaatatc cccccaaata tctataccaa 15840 aattatcaaa actaccaaga gagctaaata gaaaatcaac accaaaaatc atttttattt 15900 ctatatctta gcaaaaaaga gcttagaggt ggcatgttaa aagttaccat ttactaacga 15960 aaaggcaaat ttgttagaag aaaacataat ttaaaaatgt gcagccgggc acggtggctc 16020 acgcctgtaa tcccagcact ttgggaggct gaggcaggag gatcacgagg tcaggagttc 16080 gagaccagcc tgaccaacat ggtgaaaccc agtctctact aaaaatacaa aaaattagcc 16140 aggtgtgttg gtgtgcacct gtaatcccag ctactcagga ggcttgaggc aggaaaatcg 16200 cttgaaccag ggacgtggag gttgcagtga gccgagatgg cgccactgca ctccagtctg 16260 ggcaaaagag cgagactccg tctcaaaaag aaaaaaaaaa aagtgcaaca tctttatgga 16320 taaaattgta aaacttttgg aaaggcatta aagaatagat aaatgggctg tgtgcagtgg 16380 ctcacacctg taatcccagc actttgggag gctgaggcgg gtggatcacg gggtcaggag 16440 ttcgagacca gcctgactaa catggtgaaa ccacgtctct actaaaaaat acaaaaatta 16500 gccagccatg gtggtgtgca cctgtaatcc cagctactca ggaggccgag tcaggagaat 16560 tgcttgaacc tgggaggcgg aggttgccct gagccaagat cgctccattg cactcctgcc 16620 tgggtgacag agtgagactc catctccaaa aaaaaaaaaa aaaaagaata gacaaataga 16680 caaattcact gtatttatta ataatgacac tcagaatcgt gagtatatct gttctttcca 16740 aattattaat ctattgatcc aatataattc taatgaaaat ttcatttttt tcatgaaaca 16800 taacaagctg atttttaaaa attatgtgaa aaagcaaagg atcaagacaa gaggcttgta 16860 aaaaaaaaag aattgggcag ggcagagggg aagcaagagt ttgttctcta agatattagg 16920 atgtaatatg aagctaccat cactaagatg agtagtattg gctcaagggt agacaaatat 16980 atcaatagaa cataatagag aactaagaaa tagagcacat tatattagca agggtaatcc 17040 ttgattatgc tataatcact aataaaacct gaaacagctt tacttaatac aatatagggt 17100 taattctgtc ttagtacgtt tgggcagtta taacaaaaaa taccttaagt ggtgtagctt 17160 ataaacaaca gaaatttatt ctcacggttc tggaggctgg gaagttcatg acaaagcacc 17220 agctaattct tgtgtttggg gagggactat cttccgcata gacagaacct tcccgctata 17280 tattcacatg gtggaagggg gaggggatct cttttttaag gtcactaatc ccattcatga 17340 agcctctccc cttatgacct aatcacctcc caaaaccctc atctcctaat accttggagg 17400 ttaggatttc aacataggaa ttttgggggg acacaaacat tcagatcaga gcaatttctc 17460 actcataata ctaattgatg aaggtcatag aactctccct ggtgctctcc ttcaacttgg 17520 agatcttggc tgcttccatt atgcaactcc acatttgagg ctctttgctt ctggccgcag 17580 gatgagaggg ggcacgtgca catgaagaca cacctactct taggcaccta taacactccc 17640 acgcattccc attggcaaag ctcaggcact ggctctcaac acaaccacac ggaaggctgg 17700 gtaatgaagt ttttctgtct atgcaggaag aggcagtggt gttgatgaac caacattttc 17760 tctgccaaac agtatggaaa cttgatatat gacaaaattg acatagtgga tccctgggaa 17820 aaatatagat gatgtaaaaa atcataataa taaacgatgc taagaagaaa aaaaaagaag 17880 tctatttctt ctttacactg cacccaacca aataattttc aattgaattt aaaatttaaa 17940 taagaaggac agaagaagta tatgagaata tctttatatc ccagatatct agaaagacat 18000 cttaaaccac acaaacctgg aaggaaatga ttaaaaaaaa aaaagcacat catcaagaaa 18060 gagaaaagac aaattacaaa ctgctagaag atatttgcaa tacatataac tgacaagaaa 18120 ttagtattta gaatatataa agaaattata caaattaact actacaaaaa tacaagtaaa 18180 ttagaaaaaa atgggcagtt gatctgaata aacataacat ataagcaaaa atatgaatgg 18240 ccaataatca aatataaaca actgtacttc attaataagt cagaaaatga aaatcaaaat 18300 cacaagaaaa tttcatttca taaaaatttg attgcaaaag ttgaaaagtc agagagcatc 18360 aggtattggc aaggaggaag aacaacagga aatcttttcc actgctactg acaatataaa 18420 ttgatacaaa aaacttgagg actgatatga cactatccta tgaaattaaa actgtgcata 18480 tcccatgaaa tggcaattcc acttgtaaga aaatgctttc atgtgtgaac tgtggctagc 18540 tacttcaaca cagatgataa tcttgagaat acaatactga acaaaagaaa aacaagattc 18600 agaagaatac atatagtata ccatttttat aaagttgaat caggcaaatc taagggtatt 18660 gtttcagaat tcacacatac atgtgtttaa aaatccatgc tataaagaaa aacaagggaa 18720 tgagcaaaag tcaaaattta aggtagagga tacctctggt gatgtggcaa gggggtagga 18780 cagagaggag cacacaagga tcttcaggat gtcaaggaag ctggactttt taagtggggt 18840 gatgggttca caggcattca ttttattgta taattaacta ggatcagcat aaatattccc 18900 ttatgcatca aatatttaat ttttaaaatt aaaacacaca tgcacgcaca agaaaaagga 18960 aagaagtaaa tactctgtaa actgaccccc agtcaagaga gctgttgatt ttgcaattgc 19020 ttaggagcat aaagactgag agtatatgtt ctcttattac actgaatctg tagtaagatc 19080 ctctgtccta ataacatttt aaattttgtt tcccttttgc aattacctaa aagctcctca 19140 cagtataata tattccatct ttactcttta tttaatatca aaatcctctt ttattttttt 19200 ccccagtggc caagttctag ctgctcttcc tagaacctct aggcaagttc aagttctaca 19260 gaatcttact acaacatatg aggtaatttc tccctaattt atgtttatat tggtttcact 19320 ttgtataagc actgggtgtt gagtttcctc ctgtatgttg tctggcttac atgtatctgg 19380 tatgaactct tcttctcata gtcttctctc ccttctcata atcacatgat tttgttggtt 19440 ccccaaatca acacttcttc acttgtgcta ttggctttcc agccaatttc ataatagtac 19500 cttgggatat aaagtgtgca cttacaaaga ggctacagta acagaaatta aaatatttat 19560 aaataaaacc ttactcatga aacaatggtt cttaaccaag gatgcaccag aaagacagag 19620 tacatttatt aaaattctca cccaggcacc catctcgaca taatgtctaa gatgtagaaa 19680 attgacaaga attacagaat attaatggca gtggcggccc atctagagcg gctgctgcca 19740 tgcgggaggc acggctgggg ctgtgtgctc cacggagcca gcagaagcca ggaggaggta 19800 aaagtcccgc ccccttctgt gatggcaggg cggcagcctc atgctcccca ggcgcagctg 19860 cagctgcccg ctgcagctac agacctggac atccctgtgc tcttgggggc caggagcagg 19920 caggagccct gccctcctgg gcgcagctgc agctgcccag ctggggttgc agacccaggc 19980 atttctgcac tctcagtgtt ctgagaagga ccctcattcc cctacaggct cggaagtgcc 20040 tgctcccact gtctggtctc tccgagttcc tggtgctcac tccaatcttg gagcaaaatt 20100 gaggctgagc ctaggtgttg tcacaacctg gctggctgtg tgcatgatca gagcggtact 20160 gacatgctag ccccctgctg cctcagcccc ctctggactt tgggtactga cgagcacagg 20220 agggaagcca agggggtggc tgagggcttc tcggcactgg cctgcaggcc ccctcagctg 20280 gaaaatcctg ggtgccataa atagccgtag gaggcagaca ggatcctagg cagaaaaggg 20340 cgggtccctg gtgaagcccc accttcaagc ccaggaaggc tgccagtccc gtggaccgca 20400 gtgggaactg acggtgattt ttccgcaccc gcctatggcc acccatgaac caatcagcac 20460 tcacttcctc ccatctgaag cccatagaaa tcccccggat tcagccagac tcttctggag 20520 agacatgggg aggaccagct gtagagagga gccacccact ccagggtctc ctctctgctg 20580 agaactaaca ctcatcagga caccctggct gcagagagga gctacccacc gcgagtctcc 20640 tctgagctgt tctattactc agtaaagctc ctcttcacct tgctcaccct ccgcttgtcc 20700 acgtacgtca ttgttcccgg gcgctgaacc tgccaaatgg tggaggtgaa agagctctaa 20760 cacaaacagg gctgaaacac gccccttgct tgccacgttg tgggtgacaa gaaggagaga 20820 agagctgcag ccttttgggg agctcagacc taagaactcc ccgaggcagg actatgacac 20880 cctctttagg gctctgtggt tcctgacgtc tccaaacttc tgggtgccac caccttcccc 20940 ggtgccagcc attgaagctg cttgagggac acctggtcca gccacagcct tgcagggagc 21000 cgaaagatgc ccaccctgcc gcagccagca tgcctcgctg tgtgtagtag ctggacccca 21060 cacctgctca ctcacacacc cctcaccgct cagctcgccc ttggcacgaa tgagacccaa 21120 gccagtagca cgagatgagt gcagcctgcc aggccgagtg ggctcagcgg gcctgagcaa 21180 agcttaggca aaggcgccac tgaccacaga ggtttctgct ggtgaagcga ccccagggat 21240 cctgtaacaa tatcatggta caaaattgat ggctccttgt ttgttagtgt tttccaagaa 21300 gcagaggtca agactagact ggaggagcaa gcgatgaggg gaatgctgtt ggaggataga 21360 ggcgggagct ggagaaggca gagagcatca tcagaccatg tcatagctct gacacctctg 21420 cagaaagggg aattttgttt ggagaatctc agactatagg gcaggtccaa agaaggctgg 21480 gctaggtcag tctcagtctg gcaagaatgg gcctgcatta acacttccac aggactcggt 21540 tactggctgg atgcagccct gagaccacat ggcctcagct tctagtgggt caccagggca 21600 gccactgaaa acaccagcca actgtatttc tctcaaccga agagctaaat ggtgcatatt 21660 cacgaccacc acatcatggt aaagaggaaa tactacaaga ggaagcatct gagatttaga 21720 attctagttc ttgttctgtc atttctaggt gtatgatttt agatgtcagg tatgaacctt 21780 aatttcttca cctgaacaat gcaaataata acacctgcct agtctatatc aaagcgttat 21840 aaatatcaaa ggaaatgagt gtgaaagtgc tttgaaaaag tacgtgtagt ggctcgtgcc 21900 tgtaatccca gcactttgga gggccgaggt gggcggatca cgaggtcagg agatcgagac 21960 catcctggct aacacggtga aaccccgtct ctactaaaaa tacaaaaaat tagccgggcg 22020 tggtggcggg cgcctgtagt cccagctacc cgggaggctg aggcaggaga atggcgagaa 22080 ctcgggaggc agagcttgca gtgagccaag atcgcgccac tgcactccag cctgggagac 22140 agccagactc cgtctcaaaa aaaaaataaa aaataaaaaa taaataaata aataaataaa 22200 aagcacatta agagagaaaa aatgtaaatc ttattggaag cctttttaaa aaaaggaaca 22260 atgacatgat gataattaca agaacatgaa atttttatta aataaaatca atgtttaatc 22320 aactttcttt ctagaaaaaa ttttgtttcc tttcaaatat ctgatgtaca catgcaattt 22380 tacagttaag ccatgaatat agtcattcat tcatcattgt ctcatcaaat atttatggat 22440 tatcttgtat attccaggcc cttttatttt attttttttt agcaactaga gttatagaaa 22500 ggaattttaa aaaactcact gcaaaataaa tgtttatatt accatgtgtg tggatgggga 22560 ccagcaccag ggagtgtcct tttcatactc cttatagata aaactgtcat ggctctagct 22620 acagatgaga atgatgtgaa caactctttt ttaattttat caattttgcc ccttaaactg 22680 tagattgttc tctggcagcc ggtaacagct gaccttattg tgaagaaaaa acaagtccat 22740 ttttttgtaa atgcatctga tgtcgacaat gtgaaagccc atttaaatgt gagcggaatt 22800 ccatgcaggt aggcaccgtt caatacgtat tgagtagtta ttataaacac ttactatgca 22860 cttgactagg gtatggtata attgcttcct ggaaaaataa aatgtattaa ccatggcagc 22920 atagaagtct ctgactggac caaatggact ggtgataaag cctaaggtcc agctctgtga 22980 tcttggataa atggttcaac ccctcatgac ctccgtccct tatctaaaat gcaggttaga 23040 ctcagtgatt ggtaaaggct ctcatagttc ctttttctct gactctgtac ccagactcag 23100 ggagcaaaac tgtcatttgc cttggtaggc tttttgatat ctcctgaaaa agcagcttcg 23160 ggaggggatt tagcttctgc taattcttct tcacaaagac agtgaccatt tctgaatgtc 23220 tggctttaaa aagtgtaaca ggtggttgga ctctgcagag acctcgggtt agtctggcac 23280 tgccccttac cacctatatg accctggggg aattattcac ctctctgctc ccaagttttg 23340 tatattaagg gtaaaaacag cacctaccct gtggattaga aatgatttcc ttttcttaaa 23400 aagtgtatca ggtacaattt ctgctcacag tctagccttc ttcttatgga gtctcctaat 23460 atctcccctc catatccact gcccaactgc cagtaccttc ctggtggcct ggccccttga 23520 gaccatgctc tcttctgtgt atcaatgggt gccccctgga taatatgcta tgttaattat 23580 tagtaatata ttatagagta tattataggt gtgtactgtt ttccaggaac tgtgctgaac 23640 ctttctatta attgacattg tgtctattaa tctttattta accccgtgaa gtagatgcaa 23700 ccccattata tagatgaaaa aatatcctta cttataaagg aatttttcag ggtaaatcag 23760 aaagaacatg gcagagttag gagtcgaact tagacctttc tgatgtcaac actgcggctt 23820 ttatttattg gcctaaataa aagtaaagaa ccctttatta gtatgatagc taactttcaa 23880 cttgtccatc tcaggcgata gaatgcctga attcagctaa aatatttgcc tggttaacaa 23940 atgtggtgct ctgaagagaa cttgaatgag atgcctttcc tgtacttccc ttttcctgtt 24000 ctatttcttt ggctctgcag aacatctgat gcaggtcaat gggggaaaaa ataagaaaaa 24060 aaaaaaaaga aagaaaaggc ttttctgctt cttcttcctc tttaactgaa aacagcataa 24120 tacagtgtta gtctggattg aacaaaggta cattaatcca tatattcata taaaagacac 24180 tgaagaatca ccattgagta atgttggtaa tggtgggaaa cggtggtttt tatggaggtc 24240 ctgaaaatat acctaatagg agctactttt tctctagtgc ccatgtaggc tctactgaaa 24300 gggtttgtca accagtttac cacaatgcga gatgtcttac ttttaccttg atgaaatgct 24360 tatgaagttt cttagtgatt ttttttcttc atgctcacct gctgtgcctg caatgggcca 24420 tgtgggaaga tccaccctct gcttggaaac tagctcactc tctgtttcat cacctagtgt 24480 cttgctggca gacgtggaag atcttattca acagcagatt tccaacgaca cagtcagccc 24540 ccgagcctcc gcatcgtact atgaacagta tcactcacta aatgaagtaa gccatcacac 24600 agctcttcaa agctactatt ttcatttaac cagtattgcc atttcaatca ggggaatatt 24660 caagaatcat aattggtgga agatggtaaa aaataaaaca caaacacact taggttaatt 24720 aaatggtggt cattcatttt ttggtagatc tcttccctga gaagactgca tcatatttgg 24780 taaactgcag gatgtttgtc tacagctaag aatatctcta actgctggga ataacacttt 24840 atgctatgga acaacagaaa ttaaagaatt ggggctttta attaaaactg ccaccaaaaa 24900 attaccagtc caattaatca tgtctctttg gaccattacc ctaattttac taattaccag 24960 attagctcac tgaattaaag gaatatattc acttatattt aatacactat aactaattgc 25020 attttattcc ttagaaggaa gctatttaaa ctaataataa taataatgcc tttgttttaa 25080 tctgtaagaa attggatttt ttttctatca gtacttacag gttccactcc ttctagagag 25140 aacttgagta agatgttgat gtgcaggtga gacctcagca agctttcaca taatccacta 25200 aaagccattc cctgtatttg ttagttgaaa gaataaattc gcaggaggac tttctttttt 25260 atatgatatt ctccaagtag taaaaatacc ttgatgcctt tttatgagta tgcagctata 25320 ttgcctaata taactatttt tgtcatcttt gactaagtgc ccagaaacta ttagggacca 25380 tatccatatt tttaagacat ctaagactta ggtaatgaga atcaatttta tgtatataat 25440 ctttaaaagc atctgttcct tcccagttaa ttaagccaga gtcagtatgc ttctagaatg 25500 tgtgcctggt tgattgaggg ggccttaaaa ttgcaccccc ccttttttaa tctctcctac 25560 atctatccaa cttagaccac ctctctccag catccatcag cacgactgca tgagcaaact 25620 tgatgcagag aggcttcata ggtgggattt caccttcata gaaggtgaaa ctgtcactgc 25680 tgtgataagt ttggtgggga gaggggaatg ccgtaaacag aagtattttt aaatatttgt 25740 taaaacatat tttaattatt ttgttcaaaa aagttatgtt ttcttacgat atgttcagga 25800 aagagttgga atgacacagg aggaaaaaat aagcacatgg ctctattagt tttctagggc 25860 tgtggtaata aaataccaca gactgtgtag ctgaaatcac agaaatttgt tttctcatga 25920 ttctagaggc tagaagatca aggtgtcagt aggtttggtt tctactgagg cctctttcct 25980 cagcttgtag gtagttgcca tctcacagcg ttcttcctca tatgcctttt ctttcctttt 26040 tttttttttt ttttttgaga cagagtttct ctctgtcacc caggctggag tgcgatagca 26100 tgattttggc tcactgcaac ctgcgcctct tgggttcaag caattctcct gcctcagcct 26160 ccagagtagc tgggactaga ggcgcatacc accacgctca gctaattttt tgtattttta 26220 gtagagatgg gatttcacca tgttggacag gctggtcttg aattcctgag ctcaagtgat 26280 ctgctcgcct tggcctccca aaattctagg attacaggcg tgagccacca tgcccagcct 26340 catatgacct tttgtttgtg cacatgcatc cctggtctct ctctgtatat cttaatctcc 26400 tcttcatata aggacaccag tcagattgga ttcgtgccca ctctaagggc ctcatgttga 26460 cttgatcatc tctttaaagg ccctatctcc aaatacagtc actttctaac ctactgggag 26520 ttagggattg aacatatgaa ttggagaaag gggtacaaca tctactcctt aactatgaca 26580 ttatagaaaa tgtcttgtgc ttctctttgc acccccgccc ctattatttt ctaacaggtt 26640 cataggaacc ataagcattt tgctctcaga atattcctct aagtgcttct ttccctttga 26700 tcggtggtct cttgatcagc cctacctaca agatggactg gtgggcagca gaggttattt 26760 tgtcattgac tcacaccagg agatcttaaa tgatccggtg tagggagaaa gaaacaaatg 26820 gccaaaaatt acttcttaga agaaatggtg agagaaaaga gttcttcaaa ggatgttaca 26880 ttattacccc agcttagttt gagaaatgaa taaagtctgt cggttaaact gccttcatat 26940 tatacagcct ctcctgttag aggaaatcta ctgaagtatc aatgcataaa ttattttttt 27000 gtggtagctt tctcagatgt atttatgcct agaagagtaa cacaggaaat ggagattcaa 27060 ttaggaaatt gctgacagtt acatttctga caccccagac actgacaggg tcggtacttg 27120 gtggcaggtg ggcaggagcc cttaattctc agcatgggga caaccactca cacctaccac 27180 tcatgctggt tatgtgatct cagagaaccc aaggataaat ggtgctccag tttttaccag 27240 ctaggattgc tatttgaaat cacctctaga aaagttccca gagataaagc cagggtttga 27300 ttgcttctgt ttcagaaggc atcagagttt aagaatggac cctggaaagt tggtccaaat 27360 taaaacataa cccagttcaa tcccagcaat cccaaaccag acaataattc aatgtttgct 27420 ttgaagtggg tgctagccta aagtcagaat ttttttcttt tcttttcttt tcttttcttt 27480 tttttttttt tttttgcttt ttccttcccc tattatcttg acagaacctc aaatacaact 27540 ggacttccac ccaagagaga ggtccagaat cgaactactt cttgggggga taattgagtt 27600 tgtttgtttt tcctccagat ggtccccacc tttgcctctc atcattgtgc caatctcact 27660 gtgcttgcac aggtctttag tgggaaacaa tgatgcttcc atttatcctg catgaagaca 27720 gtgctaaggg ctcccttcat cttgaaaagt gcatttttaa aaaagtctca tataaaagtg 27780 aacttttgaa tgaatgagaa caagaatttc atacacaggg gcagtgactc aatgtgatga 27840 ctttaaaagt aactttcagg ggccatagtt tatagattaa cttttcctac ctcattataa 27900 gtatcttagc actttttcac tctttctcaa aaccttgaca cttatcaaaa ctttaatttt 27960 attaatttcc ctaaacagca gaagaaacac cctgccctaa gtgctttagg tcctcgtgca 28020 ttccacatac agaggttttc ctttctctga agaagttgtc tgcttgcttt ggtcagggaa 28080 atgctttgaa cttggcttcg tgactaacct ctggtttcca ttttgctaga tctattcttg 28140 gatagaattt ataactgaga ggcatcctga tatgcttaca aaaatccaca ttggatcctc 28200 atttgagaag tacccactct atgttttaaa ggtatgttgt ggggaaagtt gttgatcttt 28260 cactgtgagg ggagggatta attctccagt cgtgtttgtt aaaacttgag tttgtttcct 28320 ttgagttctg aaaatatttg cattacaagt gttcctcaac tttaatacct ggctatttag 28380 gggttggtta tttttcccat taataatata gtcttgtcct ggtctgtatg tcctaatctc 28440 ctcccacaag gacaccagtc agtctggatt agtacacacc ctaagggcct catgttaact 28500 taatcacctc tttaaaggcc ctatctccaa atacagtctc tagggggtta aggcttcaat 28560 tctagatgaa tcccagttct agaattaact ctgtttctgt ttatgtgaca ttagataagc 28620 catttaacat ttccataaaa tgaaggaagt ggtgtttatt tttttcaagt ccttgtttta 28680 ttttcgttag tggacaaaca ctatttctgt taggggacaa acactaacag aaaataaaac 28740 agggacttga aaaaataaaa ttaaaaatta aaaaaagtgg tgcagctttt tgatgttaat 28800 ttttaaaaat tgatacataa taattgtaca tgtttctggg gtacatgtga ttttttttct 28860 ccctccctcc tcacatgtga tgttttgata catgcataca atgtgtaaat cagggtattt 28920 gggatatcca tcacttcaaa catttatcat ttctttgtgt tgggaacatt ttaagttcat 28980 cttctagcta ttttgaaata ttgttgattc tcgtcaccct actgtgctac tacacactag 29040 aacttattcc ttctatctat tttgtaccca ctaattaatc tctctttatc ctcctttccc 29100 agcctctggt aatcaccatt ctactctcta cctctatgag atcaacgttt tccactcccc 29160 atatcagtga gaacatgtag tatttgtctt tccctacata gcttatttca gggcatgttg 29220 ctgcaaatga taggatttta ttccttttaa tgcctgagta atattccatt tgttatccac 29280 attttccaca tgcatatcca cattttcttt atccacatcc acattttctt tatccattca 29340 tctgttgaag aacacttagg ttgattctat atcttgacta ttgtgaatgg tgctgtaata 29400 aacatgggag tgcaggtatc tttttgatat actgatttcc tttcttttgg atacataccc 29460 aataatagga ctgctggctt atatggtagt tccattttta gttttttgag gaacctccac 29520 atggtttttc atagtggctg aactaattta cattcctacc aacagtgtac aagggttccc 29580 ctttctccac atcctctcta gcattcgtaa ttgcctgtct tttggataaa agccatttta 29640 actggaatga gatgacattg cattgtggtt ttaattcaca tttccctgat gattagtgat 29700 gttgaggatt ttttcatata cctgttgccc atttgtgtgt cttcttttga gaaatgtctg 29760 ttcagattcc tttctcattt ttaaaattgg attatttgtt tttttccttt tgaattgttt 29820 gcgttcctta tatattctgg ttattaagtc cctgttggct ggatagcttg cacatatttt 29880 ctcccatttt tttcttttca cgctgttatt tcctttgctg tgcagaagca aattttcagt 29940 ttgatgtaat cccctttatc tatttttgct tctgttgact gtgcttttga gatcttaccc 30000 aaaaaatctt tgctgagacc aaagtcctga attgttttcc caatgttttc ttctagtagt 30060 tttatagttt taggtattac atttaattct aatctgtttt tagttgattt tatatataag 30120 gcgagagata ggcatttagt ttgaatttta tgaataaaat ttttcccaat accatttatt 30180 gacaagactg tccttttccc aatgtatgtt cttggtgcct ttgttgaaaa tgagttaact 30240 gtagatctgt ggatttattt ctgggttctc tattctaatc cattggtcca tgtgtctgtt 30300 tttatgccag taccatgctg ttttagtact ccagctttgc tcattctgtt cagcattgct 30360 ttggattttc aagatctctt atggctccat atgaatttta gaattttttt tctctttcta 30420 tgaagagtat attgatattg acagggattg cattgaatct gtagattcca ttcggtagta 30480 tggacatttt aacaatatta attcttaagc ccgtgagcat gaggtatctt ttcatttttt 30540 tgtgtgttct cttcagtttc tttcatcagt gttctatggt cttaattgta ggtctttcac 30600 ttctttggtt agatttatta caggtttttt ttttttggtc attgtaaatg gtatttcttt 30660 cttgattttt cttttaggtt gtctgctatt gttgtatata aatgctactg attttgtgtg 30720 ctgattttat aacctgcaat ttactgaatt tatcagttct aacacagttt tttggtggag 30780 gctaggtttt tctaaatata agatcgtgtc atctaaaacc aaggataatt tgatttttcc 30840 cttccaattt agatgccttt tatttctttc tcttacctgt ttgctctggt tagtacttcc 30900 tggtacagct tttgaaacta aagtaagacc aggacaacaa atcccagcga gggacaaaca 30960 gccggacaag gctgaagtcc tttgcagtag ggttcttatg atggtttcta ctccaatttc 31020 cacccatttg gttatttatt ttcagtcgca aaatattatg caagagaaat tgattaacct 31080 aacttggatt ggatgtcttc tctcttgaat aaattgacct tagtaaaggt cagtgaacat 31140 agccacagcc aattgttttc agaactagga aacaactcta tagttctgtt ttctacctct 31200 ctctcttaaa aaaaattttt tttaaagctc tggaaaataa tgtagtcact aaaaatgtac 31260 atttaattta gtaacatata atttatgcac agtatcccaa tattatctaa attgtgatag 31320 gtgagcctct tcagtcattc aaagataaga ctttgggtta ggacttctca attttaatct 31380 gtcgtttaca agaacttaca gtgcagactc aaggcagaca tatgaaatgt tgggtcccct 31440 tggttattga gttggtcaat cagattggat ccatgtatca tggcatatcc acccatgaca 31500 tttgctttca gccatgttgt gtgtagtcct tggaacatac ttatctggaa cctgtacacg 31560 ttgaaaaatc atgcattctg gatggtttgg tcctactctt acttgatcaa ggatgtgcag 31620 ataatgtgag tctctgggat tttgccaact tttcggtgtc agaaccagtg ccaagaaaat 31680 tggcccagga cttagaaagg tcaagtaaag taatgaatcc agacaactta agattttctt 31740 tgcattgagt agattaagct aggtagttct ctttgactat acaatttgac gattagtggc 31800 caatgccatt gggctttctc acttactatc ctgttaaata ttgctagctc caagttagga 31860 aaaaacctcc tggagtggtt caaatgacaa tctaaatatc taactctttc tttttcttat 31920 tttggaattg caagtctaca tatttgtttg attttacaac agtcttctcc cttccctcta 31980 taccagtggt cctcaacccc tgggctgcag acaggtacca gtccatggcc tgttaggaac 32040 gaggccacgc aactggagat gaatagccag cgagcaagca ttactgcctg agcaatgctt 32100 cctgtcagat cagtggcagc gttagattct cataggagca caaaccccac tgtgaaccgc 32160 gcatgcaaag gatttaggtt gcatgctcct tatgagaatc taatgcctga tgatctgagg 32220 tggaacagtt ttatccccaa accatcccca ccactgattc caccccaact ctgccccatc 32280 catggaaaaa ttgtcttcca tgaaactggt ccctggtgcc aaaaaggttg gggaccactg 32340 ctctataccc taaactgtgt tgtagctgac ttttaaaggc aaatacatta tgattaattt 32400 tggaggtgtt cttgataatt cttctaaaga catcaaaggc tattattgag aaaaggttga 32460 tgattcttat tccagagtta gcagcttgtg ttagcccacc atactgggaa aaaagcctct 32520 gtccctggat ttgctggtaa gttcgtgaga ggttagatgt atgcttcttt ttgtgtgaaa 32580 taaagaaata atccacataa aaaaatatgc actcaggaaa atcttgaggg agtttttgct 32640 ccgggtgtgt ctccacacct cccggggaag attgccatcc aactcacacc catttacctc 32700 taaatgaagc atgaagatac agcccaaatc attagttctc tggtctcttc tttgaaactt 32760 ccacatgcag ctctgacatg actgcataat tgtggaggat aaaaacagtt ttaaatcaaa 32820 gagtcctggc ttcaaacttc agtttcaatt cacaccagct ttgctacctt aactaatgtc 32880 acttagtatc accagtgttt aaatttccct tgagaatttt caaagaaatg cagaacaatg 32940 catatctcag agatttgctg aaactattaa atataagcac tatataaatg aaagttatta 33000 tcctgaagct tattgttact gtttttgcta cttttggggt ttctttgagc aggtttctgg 33060 aaaagaacaa gcagccaaaa atgccatatg gattgactgt ggaatccatg ccagagaatg 33120 gatctctcct gctttctgct tgtggttcat aggccatgta agtattcaca ttctcttaac 33180 cctatttctc aaaatggtgc ccaagatcac ctgtgtcaga ctcaactggg ctatttatta 33240 aaatgcattt tcctaggtca catcatgaag cttgggaatc tacaattttc acaagtttcc 33300 caggtgactt ttatgcatta gtaagttgaa gaacatgact tcaagcattt aaatcaccca 33360 aaatattttt ggtcttttct acattaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaga 33420 aatagtacat tgattataat atgtttacta agtagaggaa aggactgaag gagttatcta 33480 agttggggcc caattaattt atttctcttt tggttttaat tatccagaca tcttttgcca 33540 cctttgccct tggaaattga acataaagca caacattaca gaggtgaaac agaatatgtt 33600 ttctcatatg tcataatagg gaattttctt cctgaagaag ggttttgcat caaaaaagcc 33660 atatataaga caaactgtat gttggaaaag taaaagatat aacgactatt aacctccctg 33720 atgaatgaaa acagtaaaaa ttatgcttca aatcctataa aatgggcata tatgttctct 33780 acactgattt ctacaaagaa tcatagccac tggaaaaata actcaaaata tgtgtctttc 33840 tgataatgat ttttgcagtc tttgcattca cagatacata gtaacagaat aaatgagtta 33900 ggaaattaag atattggcac ttattaagta catcaagata aaactgtttc tgtctttgct 33960 tgaccttgac aaatgcaaca tccctatttg ccttcattca ctgtgaatct tctatcctcc 34020 attctccatg gatgggagct gcaacctccc tgagtctact ggaaattccc aaacaccatt 34080 ggtactacct tggccaaatg aggatgattc caactgatca gacccttaac atatcccagt 34140 cacatcatga tctggaacct tccccaagtt gagtagtttg gttattttag gtagtgaagg 34200 gagcagcagt taatagagaa aggtccaaag taggagagta agaacattta ttttccattc 34260 tatcactgaa catgagaagg gccaagaaga aacctccatt catattgact ctaatttata 34320 tcggtgaggt tgtccctaat gactgccctt ctcaccctga cacctctgcc ctcctattag 34380 acatcctacc ctctacccaa actgcttgct gaatctttgt aagattaaat tatttaatcc 34440 acaaatattt ataaattgcc tatgatgttt cagatcctgg aaatacaagg atgaacaaaa 34500 tatagcccaa ggatcttata gctgagtatt ttgctccaac aatgtgaacc tgatttgtgt 34560 agcccaaaga aacataatca ataagggctt tttaaatcga catttaaact ccattcttgc 34620 ctgcctaaaa ctaattcaga tcatctgact ctcttagtac ttcaaagcac tggaggaggg 34680 aaagtaaaat aaaatattta cctttcaaca attgtgaagg caggttttat attcaaaaac 34740 taaaccaccc aaaggcaaat taaaatctta gcttttaagt ctctcactct tttctacaac 34800 tcaataagga tttcaaaaat cttataatct agtctcagtg gaaatccact acactacact 34860 ttgagaagct tgaagccagt catttctttc taagcttctc attcatgtac tctcgggagg 34920 caaatttaga tccttctctt tccgcaaagg cagagctgag accaatttgt gcatgactgc 34980 atcaccaagc caaaatccgg cacagggctg gcacatcata ggacccagtg aatatatgtt 35040 aaccatcaca acttgccaag tactttttct gccaaatggc ttttctcact gctaacctcc 35100 tgccaaacct ctgccctaga aaactctcat ctaattgcac acaaagttag agctctacaa 35160 cctcagggcc ttcacagaat tatctctgcc cctcctcacc acagctgaca catgacctaa 35220 ggacactgct ccctggtggc tccttcaagt agaggggctg ctcttttttt cacatcacca 35280 tgtgctgaga ggcctggtgg agtggatcag cattctcttc tcctgatact accaatgatc 35340 cttctcttct cagaaactta cacaaactgg ttgcactctt attttattgc tatcgtgcac 35400 tgaccttcag ataatttcct ggtatccggt tcatgattct ttattcccct ccaactcttg 35460 ccatcattct gagtgaattc aaagtccatg tgtgagagtc acctaacaat gtatcttcac 35520 agttccttgt tctctgttct actaaacctc atctcaactc ctctttagca gatttctcct 35580 gtagccatcc tctggatctc agaagtaatg ttttgctgat ccttagaccc agaatgtggc 35640 catggacagc aacaaggaat gttagaagaa gccatctagc aatgtaactt cttaatttcc 35700 tgtcttctct catttctcac ccctactatg actgcttttt tttcaacctt agcatatttc 35760 tagttcctac acagatctat atcattttaa tttatcagtc cctttccagg aacactttct 35820 tcactaattg gtcccatcac aaattcatcc gaaccctcaa tttcttgctc ccttgacctg 35880 ctcttctgga gttccaaccc caaacactcc acagaattaa ccatcctttt tctgagccac 35940 cttgtacatc ttgccattgt ttattatcat acttatatta atagcattga actgctgctt 36000 ttccctttcc aacttatcac ttctattagc tttctgaagg cagagaccaa gtctaaagta 36060 atttttttgt tccccataac ctggtatatt gtttggtcaa cataattggt gctcaatatc 36120 cccttgtgga atttgaaatt taaattaatg ttgcaggttt aggctgacat acaattttgg 36180 gttgcagaga gtatctaaac agtacctact gttgggataa atactttatt gtcattggct 36240 acagttcaaa ctatacatac atatatagag attggagtaa aaactgagac agatagctct 36300 ctgatatatt tgtaatggta atgaaaatga cattttgttt taaaattttc ccttcatgtg 36360 tcttatattt ttttttagca accccattaa ctgacctata tgtcgttatg tactaattta 36420 ttatctctca aatggtcatt ggttaattcc taggcaggaa ttgttgttgt tgttgttgtt 36480 gtttagggcc acattaaagg caaagcttga gtgcacccca ggcaaagtga gaggaagagc 36540 tgagtaatca ttgaccacag gccagctgat gggaatcaat cccaccctct catcactcag 36600 tcttacactc ttctccattc tcctctattc tcatcttctt tttcttttat acagaggctt 36660 ctcaatttat ggtggggtta tgtctcaata tacccaataa acaatcacaa ctgaaaatat 36720 tctaagtaaa aaatgcattt aatataccta atctaccgag tactgaatat catagcctaa 36780 ccttccttaa atgtgctcag aacacttacg ttagcctaca gtagggcaaa atcttctaac 36840 acagagccta atttataata aattgctgaa tatccatatc acttattaaa tactgcacta 36900 aaactgaaaa atggaatggt ggcatgggta tggtttctac tgaatatgca ttgcttttgc 36960 gctattgtaa agtcaaaaaa tcataagtga aatcattgta tattgcagac catctctagt 37020 aggacaggat ttcaattatg ttacttgcca tgttggtaaa tcgtaccttc aacaaatatt 37080 tatttgtcgt caggcaaaat ttcttcagcc actttgaaaa acaatgtgga agttcctcaa 37140 aagattaagt atagagttac catatgaccc agcagttcta ctcctaggtg tatacccaag 37200 acaagtgaac acatatgttg acaaatgatt atagcaatat tattcataat agtcaaaaag 37260 tggaaacaac tcaaatttcc atcaacttat gagcagaaaa acaaaatgca gcatattcat 37320 gcaatgaaac atcaatcagc aatcaaaagg aatgaagtac tgattcatgc tacaacatag 37380 atgaatcttg aaaatactat gctaagtaaa agaaaccaga tacaaaatgc cacatatatt 37440 attccattta tatgaaatgt ccagaatggg caaatccaca gagacagaaa gttcattagt 37500 gattgtcaga ggcttgggga aatggcagga gggaaagggg agtgagttat aatgggcaca 37560 ggcatgggga ttttttatga tgaaatgttc caaaaatcag atactagtga tggttgcaaa 37620 actctatgaa tacaccaaaa accgctgaat ttcacacttt aaaatggtga atttctggaa 37680 tgtaaattat atctcaataa gctgttaaag aaaaaatggg caccccttcc ttcgggattg 37740 tagctatagc cacacttgaa ggtgtggctt ggcacacagc acagactgta tttcagccct 37800 cactcactcc ttctgtctgg agtcctacct attagataaa gaaataggta acattgttct 37860 gggcctaaca tcggtaatct ctcagagcat aactttttgt agaaagattc ccatccaacc 37920 agaggtaaat gtaggaagga aatttaaaaa gtgaagcaga aaaagaaatt catatgctgc 37980 atctattaaa agtttggccc atgttgtaga aatgaaaatg agaaatgctt tattatttgc 38040 tttattattt taaaaggaac aggctctcct aatatttttc taataatgaa tgctacatta 38100 ttactgaaaa gtgatgctaa cataaattta taaattcgta gcataaaaat gtatttaact 38160 ggttgctcga ctgtttaaaa catggcttcc ctggaaacca tcattctcag caaactaaca 38220 caagagcaga aaaccaaaca ccacatgttc tcactcataa gtgggagctg aacaatgaga 38280 acacatggac acagggaggg gaacatcaca caccggggcc tgtcgggggt ggggggctag 38340 gggagggaga gcattaggag aaatacctaa tgtagatgac gggttgatgg gtgcagctaa 38400 ccaccgtggc acgtgtataa ctatgtaaca aacctgcatg ttctgcacat gtatcccaga 38460 acttaaagta taataaaaaa caaacaaaca aaaaaacaaa acatggcttc cttcattcta 38520 caaattttgc ttccttttca ttaacctttt atttctgacc tacagtagat tttaaaataa 38580 cttttttctt ttctttctct ccgatttcat aagtatttat tcatggcaaa gatttttaat 38640 gtgactcttg tgattgttct agggaaatat gaatataata ttttaaacgt ttaaagggaa 38700 aatagtaaag tttataaaag gcttgttttt attttgtcaa taatgaaaaa gacatttctt 38760 aacaatgtca tgagtatgct ttaaggcaac aaacaattat aaactaaatt aaatatttaa 38820 tgtaattaaa tgtgaattaa attaaaatat agcaatgttg ccacaaatta agattttgaa 38880 ccaaaagctt tgtcctagat gaaacgattt gaccagctaa aatttgtctt tatagttctc 38940 ctgcctgtac attttgtcat tttggggtaa acttctcagt caccaaattt ggatgccatt 39000 ggatcacact gcaatatgtg ccactaagct ggatgactct aaagtagaga ggaacaagtt 39060 tgagatgatg tccgttagga attcatagcc agttcctagg aaaagctacc ctaattctac 39120 agctagatga tcaaagcctt gggaaacaca ctcaattcta gcaaaacttg agctccacaa 39180 gttctaagga caatgtagcc aatatcatgt aatcacatct ggggataaaa catggtaggt 39240 agtttaagct ctgatgaaca tgaattacag aaaaaggagc taaactaaat ctaggttttt 39300 gtttccttaa atcttcttag tgggctctat ggctttaata aagaattaat tttatttttt 39360 aaggaaaatt tagaaagttt atggttcgat tgtctgcctt cattaactag gaatactgga 39420 ccacgtgtaa ggcatttatc accacttcgt agcaccctaa gttcagttct tttgaggaat 39480 tagcactctt tctgaaagtt aaatctgcaa atctaaacat gccaaatgac aaattaaaaa 39540 aaagaaaaag aaacacacta agtttagaag aacttaaaac atctaattaa atatacttgg 39600 tttaatttgc agataactca attctatggg ataatagggc aatataccaa tctcctgagg 39660 cttgtggatt tctatgttat gccggtggtt aatgtggatg gttatgacta ctcatggaaa 39720 aaggtaggag aaaaggcaaa gaagacaaat catgttctcc ttggggatat aggatataca 39780 ggttgaatta ttcatagaat tctggatcta ggcacaatgg ctttattatt aatttttttt 39840 taacttttat tgtggaaaat gtcaaatata tatataagtg cacataattg tgtagtaaac 39900 ttctatctac ccatcataga gcttcaacaa taattaactc atgaccagtc ttgtttcatc 39960 tgtattctct ctacccactt ctaccttact cattttattt tgaagtaaat cctaggtacc 40020 atatcacttc atcaataaat atttcagtat gcatttctaa aaaaaaaaga actctgaaaa 40080 aaataattat agtataatta taccttaaaa actagctgtt tctgaatacc ataaaatatt 40140 gccagtattt tcaattgtat aataactttt tttttttttt ttttttgaga tggtgtcttg 40200 ctctgtcacc caggctggag tgcagtggca cgatctcggc tcactgcaac ctccacctcc 40260 cgggttcaag agatttttct gcctcagcct cctgagccac tgggactacg ggtgcctgcc 40320 accatgcccg gctaagcttt ttgtattttt agtagagaca gggtttcacc atattggcca 40380 ggctggtctc aaactcctgc ccttgtgatg cacctgcctc ggcctcccaa cgtgctgaga 40440 ttacaggcat gagccacctc gcccggcctc ctaacttttt aaaaagtatg tttctttgat 40500 tctggatcca aataaggctc ttacattatg attggtttat atgtctttta attctatttt 40560 aatccatgaa ctcacattcc atcttttgct ctttctctct cttctttttt tccttgcaat 40620 ttatttgtca aagaaaagag tttcccatta tcaggatttg ctaattgcat taccatcttg 40680 tagtttaaca tgctcttctg tctgtatttt ctggttactc aacattgtga ttcatgtaaa 40740 attactcaag caatatgaaa tactctgctt tctaatttaa agaggggcac atagaaacat 40800 aactaggtat atataaattt agaaaaacct acttgagtag cacatataaa tactaagagg 40860 aataagatta gttggtgtga ttggaaacat ggaattacac atgaattatt tcatgtagga 40920 ggtaatttat gcagaagata tggaaatggc acaggagatt gaggaaaaag tcatctctgg 40980 tgagaggaat actgtaactg aaaattttgt aggtggaggt gggcaaatgc caaactaagt 41040 aaatgagaat tacctagcat aatgcctaac acaaatttgg tgtccaatga atggtcatat 41100 ctgtaaactg gtaataaagt atatttacac cttaacctga atcacagtgg aattcagtca 41160 ccctttagat ttccagcttc ccaactgttc tttgtatcat taccctatta ttaattccca 41220 cagtttgaga acttgatatc cccagggcct attgttgcca cggaaccaca ggcctgggag 41280 tggtaacagg ctggaaggct tggcggaggg ttggtgagag taggagaaaa gggtgctaca 41340 tcatcccaaa ctcagaactt aaatgaagta tgtgcaactc tttttttttt tttttttttt 41400 tttgagacgg agtcttgctc tgtcgcccag gctggagtgc agtggcaaga tctcggctca 41460 ctgcaagctc cgcctcccag gttcatgcca ttctcttgcc tcagcctccc gagtagctgg 41520 gactacaggt gcccgccacc acgcctggct aattttttcg tatttttagt agagatgggg 41580 tttcaccgtg ttagccagaa tggtctcgat ctcctgacct cgtgatccgc ccgcctcggc 41640 ctcccaaagt gctgggatta caggcgtgag ccaccgcgcc cggcctgtgc aactctttac 41700 atgaccaaac tttcccagtt taccccaaga acccaatagg gaatttgctt tatatttaaa 41760 aaccagagtc aaatcagcac aatcgaagaa gtcatcagat taaaggtgtc ttcacatctc 41820 caccttttct agctttgaaa ggggagtggt gaattctacc taaagagagc attttaactt 41880 atgactcagc gttcagttga gacacaaagt tattttgctt ttcttcgaag gagctcagaa 41940 tgaccctgtg cataaaatta atgtaaagga aacaagacta aacaagaagg ctaataagca 42000 gcctagtgga atgaaaggaa atctttattt gtatcagtca aaattgatca aatattacca 42060 ttatgtttgg ttcaactaaa atagtctgag tggatgtgat tgaaacccgg atagcaatag 42120 ggaccgtgca aaggaatatt gcaacaacag tgatgtgatg aagccatgca aggtatggga 42180 ttgaaggaga gaaaggcaat tctggcttca tggactttca aatgcatgtc tttcctcagg 42240 ccttgaacgt ggctacccag gttgtctgtt tgtattttgt ttatgtagaa tcgaatgtgg 42300 agaaagaacc gttctttcta tgcgaacaat cattgcatcg gaacagacct gaataggaac 42360 tttgcttcca aacactggtg tggtaggttg ttggctttat ttcttgcaat gtctcttcac 42420 tgaaagggtg atgttcacag ggaaaggccc atgaattcaa attaaataca gagctggcct 42480 gtctgaatca gggaataatt taaatgataa atgcttaggt aaatgtaatg ctgcgactgt 42540 tggccagagt cagcaaatca ctttggcctc tcctctctcc tgtttcccta tctttaaaat 42600 aagaaagttg aatcagtttt ttaagatccc ttctagcttc aaaattctaa aatctattat 42660 cttggaataa taaagaagtg acagttaaag atcctatttt aataaacaaa aacattcatc 42720 attagaatat caaagacctg agatgggggg gaggacctct cttttttttt tgagacagag 42780 tcttgctgtg ttgaccaggc tggagtgcag tggcacaatc ttggctcact gcagcctctg 42840 cctcctaggt tcaaggattc tcctgcctca gcctcccaag tagctgggac tacaggcata 42900 tgccaccgtg cctggctaat ttttgtattt tttttagtac agatgggatt tcaccatgtt 42960 ggccaggctg gtctcaaact cctggcctta agtgatccgc ccacctcggc ctcccaaagt 43020 ggctcacagg agtgagccac tgtgcctggc ctggacccct catttttaat tgcacaagta 43080 aatgtttact tctatagtgt ttgaagacat ttttttcact attcactttc ttaatttctt 43140 taataaataa tataaagaaa atataaaaat attaaaaata gtataaaaag cagcacagtg 43200 ggaatttatt atttcttaat tcgaatgagt taaggcattc gatgatgttg agttatgcat 43260 tcaagaacag tctgctttca ggagtttgaa gattttttaa agaactaaaa gtagaattac 43320 tatttgactc agcaatctca tcactgagta tatactcata ggaaaatgaa tcgatctacc 43380 caaaagacac atgcaatcat atgttcattg cagcactatt cacaagagca aagacatgga 43440 atcaatctag gtgtctgtca atggcggatt ggataaagaa aatgtggtaa atatacatca 43500 tggaatacta cacagccata aaaaagaaca aaattatgtc ctttacagca acatggatgc 43560 agctggaagg cattgtccta agtaaattaa cacagaaaca gaaaatcaaa tactgtatgg 43620 tctcacttat aagtaaaagc taaacactga gtatacacag acataaagat gggaatagac 43680 actggggact caaaaaaggg gcagggaagg agagagaggg gaaagagttg aaaaagtacc 43740 taagtggtac tgtgttcacc atttgggtga tgggttcaat agaatcccaa acctcagcat 43800 cacacaatat atccatggaa aaaacctgca catgtacccc ctgaacccga agacaaagaa 43860 gtttgctttt aggggggtag gtgttagttc actctttctt cccacccact caacattatt 43920 tttcatagta ctacatttca gaaacagcta cgaaaataaa ctaaccctga caaggagtat 43980 gcatcatcta tatttttggg ctccatgggg cccataaggg agagaagcta ttgtatccac 44040 agaaacatct tcttcctccc agacctggac cctatacaat cctatgcaca taattttgcc 44100 tatttccttt aaaaaggtaa aatttcatga ttttaaacat tttatcaaaa tcccagaata 44160 cctattaaaa cctcacaaca ttcagcctgg gaaagctgat tgctaaaaca aaagaaaacc 44220 aaacctcaca acaaagcact taccttattt ccttattttt ttccctgtct aggttagaaa 44280 ctccatgcag acagaaacca atacccatta tctagtgcag tgcctggcac aaggagggtc 44340 ctcataaaat attaactaaa tgagtccatg aatgaattta gttgctctga gagctacaga 44400 tatggtagga actcagagga agaagcagtt catcccgact taggttccag ggaatcattt 44460 agtggtttct ccctaaaaaa ccactcgtgt tcccagaggc ccaaagtttg ctgcggcact 44520 aataacatgc caggggctca caggaacagc agccatgtaa aaagaatcta agtaaataga 44580 gctgacagtt actcagcgct gagccattga catagttcat cttccagatt tcattatcta 44640 tgaatcatag atggagaaac ccgggctgaa aacagttaag tcccttcctc aagggcacgt 44700 agcaagtatg tgcaagtacg tggcagagct gggctataaa cccaagttat cagttccctt 44760 ttggaagttt ttattttatc ttcaagctct tttggtgctt gattttactt aatatttttc 44820 ttggtgaagt cagtgttatt taatttggat agccaagtag tcaaaatata ttctgttatt 44880 gtcatcaaga aatgtctcag tcccctcttg ggcatggtgc tatattgtta cgtatcataa 44940 gagtgaaaaa cagaaacaga agcagcaagc atatgggttt ttaactaaaa aaaaaaaaaa 45000 aaaaccaaat aaaaagtaat tgtaaggaac tgtccttatt accaactgtt ccagtatcta 45060 ttctgtacta tgtaagcaag acagtgagaa agaagaattt aatcttttct catccctaca 45120 actagaatgt gcccctatga ttctttatat aaaggatcca aaaacacctc acttattaac 45180 aggaagtgac atatcaaacc tacttactca ttttatgctc ctctgtatta aaattttttg 45240 tgtgtgtgtg ttggagatga gagtggaggg taggttgtag gggtgtcttt gtcttctcag 45300 gctgctataa ccaaatacca taggttgggt ggcttaaaca acagaaattt attttctcac 45360 agttgaggat tgggagtcca aaatcaaggt accagcagag tgaggtcttc ctgaggattc 45420 tctcattggc ttgtagatgg ctgccttctc tctgtgccct cacatggcct tctctttctg 45480 cacaaacctc cctggtgtct ctctttattc ctataagggc accagtcaca ttggattaga 45540 gccccatgcc tatgacttca tttcactttg tctccttaaa ggccttatct ttaaatacag 45600 tcacattggg gcttagggct tcaacatagg aatttgggag gatgcaattc agttcataac 45660 aggagtacat tatgagaacc tttggtctca aacttcctaa gatagcacca cacattttct 45720 aaaacactga gttcaactac aaagtttttg caactggctt gaatggaaaa ttctttattt 45780 ctttttctag gagactatag tgttttttaa aattattttt tattatgata aaatacatgc 45840 aatataaaat ttgccatttt aacaattttt aattgtacag ttcagtggca ttaagtacat 45900 tcacaattac tactatctat tactaaaatt ttttaattgt cccaaagaga gatttttact 45960 tattgtaacc agtaggcaat atctcctcat ccctaccttc tccccagccc ttggtaattt 46020 cttatctact ttctgtctct atgaatttgc ctattataga tatctcacag tgtgcttggt 46080 tccatgtcta tagatcaaag aatgcttgag cttggaggga tccagtggcc caagttcctt 46140 cctggtacag atgaggcccc tgaggctgag acgatgaagt agttgcccaa attaacatga 46200 ctgcttaatg gtaaagcaga gtctcgacct caagtttcct gcctcttcag ggctctttcc 46260 actaaaatgc ttgaaatctc tagaatgaca atcatagaat gagaatctga ggctcactgt 46320 ccagcatagt agccactaac cacatgtggc tatccagtgc ttaaaatgta gcttgtctga 46380 attgagacat acactgagtg ttaaatacac accagaattt gaaggcttag tatgaaaaaa 46440 gtaacataaa atatttcaag aataattttt atattggtta cacttgaaat gatactttgt 46500 acatatttgg ttaaataaat tacaatattg aattaatctc acatatttct ttttgtgtgt 46560 gtgtgtgtgg cagggtcttg ttctgtcatc caggctggag tgcagtgtca tgatctcagc 46620 tcactgcaac ctctgcctcc tgggttcaag caagtttcgt gcctcagcct cccaagtagc 46680 tgggattaca ggcgtgcacc actatgcctg gctatttttg tatttttggt agagacgggg 46740 tttcaccatg ttggcctcgc tggtgtcaaa ctcctgatct caagtgatcc gcctgcctca 46800 gcctcccaaa gtgctgggat tataggtgtg agccaccgtg cctggccttc tttttatttt 46860 tcttaaagtg gtaacttgaa aatttaaagt aaatatgtga cttgcattat atttctatta 46920 aacaaccctg gtctgaggat tcatattagg gcaccacctc tctatttagt ggttatgtct 46980 tccccgacct ccatacccaa tatataatct ctattctcta agaattatat atcacataaa 47040 agggcaggaa tattcaaagg tgaccgaact atcaaaaatg gtttatccaa tcaccttatt 47100 ggttaaaaat gaaatacttg ggaagacctt agatgttcac atttcctctc agggaaacaa 47160 ttttttaaca aacattaatg ttgtgtttgt ataataacag gaataaagca gaatgagctt 47220 aattaagaaa agcaggctct gtaaggatag tgagtagcct cagccatgga ctcctgaggc 47280 agagatgcag ctggactcag aaacagaaag gaactgggcc tggagcccta gagaggctca 47340 gtgaatcctt cctctcccct tctcatctct gtgatgcaca ctggcttctt tcaggtctca 47400 gtccacatga tgatgatgat gatgatgatg atgatgatga tgatgatgaa cagcaacagt 47460 tatgaaatgc atactacatg ccaggcactg tgcaaagcac tttgtatgaa ctagctcatt 47520 taattctcat tcaatcagca tttaatgtat aatttttcaa ttttgcagat aaggaaattg 47580 agatacagat agatttttaa aaatttaccc aaagccatat agctaataaa tggtagtcaa 47640 gatttagaat caagtaattg ggtgcttaac aatatgctgt atagcctctt attctgaaga 47700 atggttacca ccaagaatat ccagattgca tctcctaaaa tgacagtatt tacttcatag 47760 ggctgctgta agaattacat gagatgtggc aaaaatctta gcagagttcc tgacgtacag 47820 catgtgctcc acaggtgtca gctggtagta ttactatttt tactgtctgt tcaagagagc 47880 agctagactg agactagact cttagtattg atttcaagtt atctttgaag ggattcagat 47940 tggcaagcac aagagtcaga ccctatcctg agccctcaac tgtttgcagg aaggaataat 48000 ctcttgtgtc acatgcagct tgctggggct tcaccttgtg aattagggac agggggagaa 48060 gtgttggaag gcagcctacc atctcaagtg atgcaaatta taatctacca aaggaatgaa 48120 tgaacgttgg tctggcaaca aatatcacca tcccatttta tttactaaac ttactaaacc 48180 actttagcaa gttaaaagta gcactgaagg cagatttaca tattctgagc tctgaagtga 48240 ggcttttctt ttatgggcta tattgatggt agctttaaaa ctacaaatat cagaaaaact 48300 aaatttacag tggattaagg aaaatggggt ttattttttc tcccataacc ataagtctgg 48360 agacagggct ggcatctctg aggatctctt agccactttc tcaaggttgc aagggagaca 48420 ggtgctggga atgactgtta gaaggtcagc tatgtgagca gataagtatt tgacttcaaa 48480 agaaacataa cacttagtgg aactatgttc tttgcagagc cctacctaat ccattcatct 48540 aaaagtgttg caacataggt aggagaatac gttgtctggg aaaccacaaa ttacagtact 48600 atgtgcatcc cctcataatt tcaccttaac aatttcgtta cagaggaagg tgcatccagt 48660 tcctcatgct cggaaaccta ctgtggactt tatcctgagt cagaaccaga agtgaaggca 48720 gtggctagtt tcttgagaag aaatatcaac cagattaaag catacatcag catgcattca 48780 tactcccagc atatagtgtt tccatattcc tatacacgaa gtaaaagcaa agaccatgag 48840 gaactggtaa gtgctactta attatttttc tcattagcat tttggaaata aaataatact 48900 tagttgaaga atcaaaaact gggaaaaatt ttggcctcta gaaggcaaat gatagatgtt 48960 ttaaatcatg gtgtgatcct gttgagagtc accctgggtc agtgttctct aagggaatat 49020 aaagaacgtg ccttacccta acaacacaca ctttattcta gcacgtgggc ttcctaagaa 49080 aatgtcagac aaattccttg aaggttagga aggaactact actacacttg acctgatctg 49140 catgtgaagc ggtataagca aggatgagta tggaatcatg cgacagcttt gtggtcacta 49200 gcttcctaca acagcacacc acagattaag tctcaacaca gcactcattg ttttggtatt 49260 agcagcagga attgttcctg ccctgacttc cttaaccctc agggttttgg tcctattaaa 49320 gtacctccaa ttttagcatt gaggagagag tctgtttttt ggaacataac agacaataca 49380 ggaaattcaa agaggactca cacaatttga tactccctta gcacttttta gtccaagata 49440 ctgtatgttt gggttcatgg caaaagatgc aaggattctt gaaggattgt agctaggctt 49500 tgacaaatcc tcatcccaga tgctctccag acagtggaag tgttacatca acagccccat 49560 tcttgggaag ggactaattt ttaggtagta gcttgtttct tagtgactca tttttttttc 49620 tggctctctt aacagaataa aatatagtca cattacagga gctagcaatt gctgatgaca 49680 aatataagat tatttgcatt ctctgaaaat agcccattta gaacataaat gtacttgata 49740 cttgagcttt tttcttctca agggaaaact gttaaggaaa gcacctttca aaaatattat 49800 ctttgaagaa ataaaaggaa atttatcatg atttgggaag tagaattagt ctaattatgc 49860 tttttttttt ttgcatcact gccagcacac atatatgttg agagccatta cgtgtaaaat 49920 accttgtcaa tggatgttta aagaagcatt aggtaaaatc ctgcccttta agagaatgtg 49980 ttatggttag ggagctcaac cattagcaaa tgttacaaat agttgtactc taaggcgaca 50040 tagagtaact actaaatacg tggcacagac agtacaactc acttctaact agaatatcaa 50100 gggatggctt cactaatgca ttcagaggga aatgctgaga taagtgagga gataaagtag 50160 ttactgtcct tgaggaattt acaatctatt aaggggggga aaaactacaa ataataaagt 50220 gctgttgatg tcaaagatca gctacatttt agacaggcat tgaaagagga tttctatagg 50280 cagacaggga aggaaggacc ttccaagcaa agaagttggt gttcaccata agaggatgca 50340 aaagtggagg gtgatagcat cagaaagtag attaggttgg cttctgaagg ggtgtgactg 50400 tcagataaat ttgtatttca ttatgtagac aatggggtta cattaaaact tattttttga 50460 acaatgagat ggcataaaat aatatccgct gataaatctc ttgagttttt caagaaggta 50520 acagtgtata ccatgatgct agttccaatt tccgaaaagt tccagataag tgagaacttc 50580 agaatagatt tgacaaaatg aatatcaaca gacaaaatga agtcaaatgg gggtcttagt 50640 tattatcctg ctccatacca gaggcataat cttttttgat ttgatgaatc tatggaagtc 50700 attagacatt ttacacaaga agaaaataga agttgtgaga aggataagaa gtgagtcatg 50760 catgcattag gtgtttgtat gtgtttagaa aggttggatt taaagtttgg tgataatttt 50820 gttcagaaat ggagtacctc taagcctttg agatgtagtt atacttcatt ttccataata 50880 aatgagttcc caaaaaggca tgtgataatt tttttctgca aattaatata tttatttata 50940 taaattattt caatatattg aaatagttta tgtttaaagc cacccaattg tgattgccat 51000 aaagtgcaca tattttaaat taatttgttt accttattta tttgcctttt agatgaatct 51060 agattttcta cctgtatact ttgattcaat taatgtatga ttatttttta gaaacttcta 51120 cttgtcatgt ttcaaagctg cacattaact gaaattctat atctttttgc ttccagtctc 51180 tagtagccag tgaagcagtt cgtgctattg agaaaactag taaaaatacc aggtatacac 51240 atggccatgg ctcagaaacc ttatgtaagt atttcttctt atgatcttag agaactttga 51300 gctactaaag aaatctgtgt gatctgtttt tctttgtgta tttaattttt ctgaattaaa 51360 tagggtcaca tgtaatacaa ctgaattgta ataattagga acagaagcat aatagctatg 51420 acaatgctga acaaagctat attaataaat gagttactaa aaagaagcca aaatcctatt 51480 taagaaatca tatttatcac aatcaagtag gaattacaga attggcatca tactagttga 51540 gtgaagcaga aaagttcata aaacttttgc atgattccca gggccaccat ggaaggttgt 51600 gcaggttgta cactacacta atctagggca tgccatttgc atcaagtgtt ttttagtgtt 51660 agcctgttcc caagagtata gctcataaca cattacagtt gattgtcttt aatatatatt 51720 acacacacaa aacttgtgac aaactcttaa caaaaagttt tgattaattt ttgctgaaag 51780 atatttagtg agtaactcct atctacacac agtgggagga cagactgatt ttgccctttt 51840 gaagtttgaa gggagatggg aaaagaggag cataaaataa acctgtaacc aggcatcaga 51900 aaactacagc ctgaaggcca aatccaggtt tttccatttt tttttttttt aatgattaga 51960 aaaaaacaaa aagaggccag gtgctgtggc tcatgcctgt aataccagca ctttgggagg 52020 ctgaggcagg aggatcactt gaggtcagga gttcgagacc agactggcca acatggtgaa 52080 accctgtctc tactaaaaat acaaaaatta gctgggcatg gggccttcca tgtaatgcca 52140 gctacttggt tggctaatgc ataagaatta cttgaacctg ggaggtgggg gtggcaatga 52200 gctgagattg tgcaactgca ctctagcctg ggtgacagag tgagactcca tctcaaaaaa 52260 ggtcgaaact gtatttatca tgaacactaa aatatgtaca cattttagtt aacatgcatt 52320 aaactgtaac aagtcttctg gcaattgtag ctttcatgag atgcttccca aactgtatta 52380 gatagatgct aaaattataa attaaaattt tgggtcagac tttgccataa acctggactc 52440 aatttagcac ccccccaaaa aaagtcagat tattcaatta atgcggttgg aaaacctaac 52500 aagttaccta gaaaaaaatt aattggatta ttaacatgtc tttcaccaaa gtaaattcca 52560 ggtacagcat atattttcat atgaaaaccc tgcataaacc aagttgaaat ctcagtaagg 52620 agaaaaaatt cttgtgaaag gagaaatgaa tgaaaggaga aaaaaaggtc tacatgccaa 52680 acaaagctaa taacactaat gtcgttttta taagcaattg ataaaatgaa ccaagtagac 52740 aaatgaggaa ggacaattga taggaaatat aaagatagcc aataaatatg ccaaacaaat 52800 gtgcaactca ctgataatca aaaaacataa attaagacag ttggatatta tttttcgccc 52860 ataaaattat cagaattcat aattcctatt gatggtatgg gaaggggaaa tgggcaaatt 52920 cataccctgc ttgtggaagt ataaatgaat tcagttcttt tgacgtccat ttgggaacat 52980 gccgtaattg caaaaagtac agagccttag actagcaaat ctattctagg gaagaatatt 53040 ctaaagagac aaagaagcaa ttatgtataa acaagggtac tcattgtaaa gttgtttata 53100 ttagttaaaa actgaaaaaa atctaaaggt atacaaacaa ataaacattt aaatcaaaca 53160 attcccagtt tgtaaattaa tttgaaacgt ctgtatttca acaatttctt tcttcttctt 53220 ttagacctag ctcctggagg tggggacgat tggatctatg atttgggcat caaatattcg 53280 tttacaattg aacttcgaga tacgggcaca tacggattct tgctgccgga gcgttacatc 53340 aaacccacct gtagagaagc ttttgccgct gtctctaaaa tagcttggca tgtcattagg 53400 aatgtttaat gcccctgatt ttatcattct gcttccgtat tttaatttac tgattccagc 53460 aagaccaaat cattgtatca gattattttt aagttttatc cgtagttttg ataaaagatt 53520 ttcctattcc ttggttctgt cagagaacct aataagtgct actttgccat taaggcagac 53580 tagggttcat gtctttttac cctttaaaaa aaattgtaaa agtctagtta cctacttttt 53640 ctttgatttt cgacgtttga ctagccatct caagcaactt tcgacgtttg actagccatc 53700 tcaagcaagt ttaatcaatg atcatctcac gctgatcatt ggatcctact caacaaaagg 53760 aagggtggtc agaagtacat taaagatttc tgctccaaat tttcaataaa tttctgcttg 53820 tgcctttaga aatacaacca tgcattccgt ttgctccacg gtaattaggc gatggcccag 53880 aaaggggagg ggtgtcaaaa acgacaaaca tagcctctca ttccagctca gctgctcaat 53940 aaacactgtt gaacgaatga atgagtggct ctaggtactg tcaacaaatg ccgcattttg 54000 cgcatttaca acagctgttt atggtaagga attatgtaat aaaaagagaa aactcactta 54060 aattcacttt taattgggaa ttttagttct cccgggctcc cagtttcctt tcctaggatc 54120 tctcacagag cacagattcg atttccaagt cccgccgcac tcttaccgct cgcatggaac 54180 cttacgccta gagggcgtgt ccacgaaggg tggtgtctgc gcactgacga ctaatctgac 54240 ggccggaagc tgcctgggtc tacagaggaa cagggcaaac ctctgacttc cggcggcatt 54300 ttgaggcggt cctcctagcg gcctggtagt gtttttgttg ccttttctta atctacaatc 54360 tcttcgttat ttttcttcct gcgacccagt ttcgcttgac cctggagagg cggcgggcgg 54420 gttggttctg cttctcagcc atcccggggg ctcctcgcta gccaagagcc ggttcccggg 54480 agccgcgcgc gcatcgcttt ctcctcgtcg tcgtcctcct gggtccaggc gcggggacag 54540 agtcgcctcc cccgctcctc ggagcggcgg cggcggtggt gcctccggac tgcacttgcg 54600 aagggagctt ggggaggaag taagcgttct gtgaattggt gtgggtatct ggggaaggca 54660 ttgagcggac ccgtaatgcg gaggcccggg ttaccccccc ccgtctttgc ttgagtcact 54720 gggattttga gctttccttg agcatcccac ccttaactct gcaatagccc cctgtgctca 54780 ggcgtaattt ctcactctga ttatgattct ggcatttgtc taagggcgat aagtagactc 54840 agacaatagg ctgtacccct cgttaccatt tgatgtaagc acgggaaccc ttgtatggtg 54900 ttcgtatttg tgtgcgatgg aagggtgcag caatttgggc ttaaatttag aatcttcctc 54960 tatactcatt ccagatctgt tagagaaaaa catcttactt gtgattggtc ttgttttttt 55020 tttttttttt ttttccctca gcagtgataa cgatttaggt cctgggaatt gagtgctact 55080 ttatcttcac aagccttagg taggtagttt tggcaactgt cagaaacggg ggaaagtgga 55140 atagaaagaa gagagtctgt ttggcggcat tatctctctg taataggcta acgcaattta 55200 tgtggtttga aaattattta gagttgataa tacttgaatt atgttggtaa gatgttgttt 55260 gtgaagggta gtcttaaggt atttggttat actatggggc tttcaggtaa ttcgaactac 55320 tttgaaaatt atgggagtat gaagtctctt aagatttttg gatttttaaa gtagttttaa 55380 aaatttggaa aacatcttta cacctcaagt tttcgaagtc cgcgataccg ttggagaata 55440 aatacttatg cagttcagtc tatgggtata tggtgccagt tagcggggtc tagttctgta 55500 acatttgaaa ttactggctt tagtacaata tattggagcg ttttgtgaat acaatctata 55560 gattttcaaa taatttttaa tttcttaatg aactatttac attataacag atgacagttt 55620 caactagaga ctagcaaagt tgatgcaagc ttgtaacaat tgcggcttta aaaatagttg 55680 cactctgaaa ctaaggcttt cactctgtgc atctggtagg attcagtttt atcaaatgta 55740 tgcctcttac tggcttcctg attactggtc attctaaatg aacattgcat attttgagat 55800 ttgcaagctt atgtgatttt catattt 55827 4 423 PRT Human 4 Met Lys Leu Cys Ser Leu Ala Val Leu Val Pro Ile Val Leu Phe Cys 1 5 10 15 Glu Gln His Val Phe Ala Phe Gln Ser Gly Gln Val Leu Ala Ala Leu 20 25 30 Pro Arg Thr Ser Arg Gln Val Gln Val Leu Gln Asn Leu Thr Thr Thr 35 40 45 Tyr Glu Ile Val Leu Trp Gln Pro Val Thr Ala Asp Leu Ile Val Lys 50 55 60 Lys Lys Gln Val His Phe Phe Val Asn Ala Ser Asp Val Asp Asn Val 65 70 75 80 Lys Ala His Leu Asn Val Ser Gly Ile Pro Cys Ser Val Leu Leu Ala 85 90 95 Asp Val Glu Asp Leu Ile Gln Gln Gln Ile Ser Asn Asp Thr Val Ser 100 105 110 Pro Arg Ala Ser Ala Ser Tyr Tyr Glu Gln Tyr His Ser Leu Asn Glu 115 120 125 Ile Tyr Ser Trp Ile Glu Phe Ile Thr Glu Arg His Pro Asp Met Leu 130 135 140 Thr Lys Ile His Ile Gly Ser Ser Phe Glu Lys Tyr Pro Leu Tyr Val 145 150 155 160 Leu Lys Val Ser Gly Lys Glu Gln Ala Ala Lys Asn Ala Ile Trp Ile 165 170 175 Asp Cys Gly Ile His Ala Arg Glu Trp Ile Ser Pro Ala Phe Cys Leu 180 185 190 Trp Phe Ile Gly His Ile Thr Gln Phe Tyr Gly Ile Ile Gly Gln Tyr 195 200 205 Thr Asn Leu Leu Arg Leu Val Asp Phe Tyr Val Met Pro Val Val Asn 210 215 220 Val Asp Gly Tyr Asp Tyr Ser Trp Lys Lys Asn Arg Met Trp Arg Lys 225 230 235 240 Asn Arg Ser Phe Tyr Ala Asn Asn His Cys Ile Gly Thr Asp Leu Asn 245 250 255 Arg Asn Phe Ala Ser Lys His Trp Cys Glu Glu Gly Ala Ser Ser Ser 260 265 270 Ser Cys Ser Glu Thr Tyr Cys Gly Leu Tyr Pro Glu Ser Glu Pro Glu 275 280 285 Val Lys Ala Val Ala Ser Phe Leu Arg Arg Asn Ile Asn Gln Ile Lys 290 295 300 Ala Tyr Ile Ser Met His Ser Tyr Ser Gln His Ile Val Phe Pro Tyr 305 310 315 320 Ser Tyr Thr Arg Ser Lys Ser Lys Asp His Glu Glu Leu Ser Leu Val 325 330 335 Ala Ser Glu Ala Val Arg Ala Ile Glu Lys Ile Ser Lys Asn Thr Arg 340 345 350 Tyr Thr His Gly His Gly Ser Glu Thr Leu Tyr Leu Ala Pro Gly Gly 355 360 365 Gly Asp Asp Trp Ile Tyr Asp Leu Gly Ile Lys Tyr Ser Phe Thr Ile 370 375 380 Glu Leu Arg Asp Thr Gly Thr Tyr Gly Phe Leu Leu Pro Glu Arg Tyr 385 390 395 400 Ile Lys Pro Thr Cys Arg Glu Ala Phe Ala Ala Val Ser Lys Ile Ala 405 410 415 Trp His Val Ile Arg Asn Val 420
Claims (23)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/813,133 US6455294B1 (en) | 2001-03-21 | 2001-03-21 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
EP02731140A EP1395674A4 (en) | 2001-03-21 | 2002-03-19 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
CA002441115A CA2441115A1 (en) | 2001-03-21 | 2002-03-19 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
AU2002303137A AU2002303137A1 (en) | 2001-03-21 | 2002-03-19 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
PCT/US2002/008289 WO2002077166A2 (en) | 2001-03-21 | 2002-03-19 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US10/212,877 US6818429B2 (en) | 2001-03-21 | 2002-08-07 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US10/954,110 US20050042670A1 (en) | 2001-03-21 | 2004-09-30 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US12/218,759 US20090082273A1 (en) | 2001-03-21 | 2008-07-16 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
Applications Claiming Priority (1)
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US09/813,133 US6455294B1 (en) | 2001-03-21 | 2001-03-21 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
Related Child Applications (1)
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US10/212,877 Division US6818429B2 (en) | 2001-03-21 | 2002-08-07 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
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US6455294B1 US6455294B1 (en) | 2002-09-24 |
US20020137179A1 true US20020137179A1 (en) | 2002-09-26 |
Family
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US09/813,133 Expired - Fee Related US6455294B1 (en) | 2001-03-21 | 2001-03-21 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US10/212,877 Expired - Fee Related US6818429B2 (en) | 2001-03-21 | 2002-08-07 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US10/954,110 Abandoned US20050042670A1 (en) | 2001-03-21 | 2004-09-30 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US12/218,759 Abandoned US20090082273A1 (en) | 2001-03-21 | 2008-07-16 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
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US10/212,877 Expired - Fee Related US6818429B2 (en) | 2001-03-21 | 2002-08-07 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US10/954,110 Abandoned US20050042670A1 (en) | 2001-03-21 | 2004-09-30 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
US12/218,759 Abandoned US20090082273A1 (en) | 2001-03-21 | 2008-07-16 | Isolated human protease proteins, nucleic acid molecules encoding human protease proteins, and uses thereof |
Country Status (5)
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US (4) | US6455294B1 (en) |
EP (1) | EP1395674A4 (en) |
AU (1) | AU2002303137A1 (en) |
CA (1) | CA2441115A1 (en) |
WO (1) | WO2002077166A2 (en) |
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AU2003213676A1 (en) * | 2002-03-04 | 2003-09-22 | Bristol-Myers Squibb Company | Novel nucleic acid molecules and polypeptides encoding baboon tafi |
AU2003279829A1 (en) * | 2002-10-04 | 2004-05-04 | Incyte Corp | Protein modification and maintenance molecules |
US7977081B2 (en) * | 2004-09-27 | 2011-07-12 | Merck Biosciences Ag | Recombinant carboxypeptidase B |
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US5206161A (en) * | 1991-02-01 | 1993-04-27 | Genentech, Inc. | Human plasma carboxypeptidase B |
US5985562A (en) * | 1997-06-03 | 1999-11-16 | Schering Aktiengesellschaft | Method of detecting thrombotic disease risk associated with plasma carboxypeptidase B polymorphisms |
ES2260011T3 (en) * | 1999-04-30 | 2006-11-01 | Akira Matsumoto | CARBOXIPEPTIDASA B OF THE HUMAN BRAIN. |
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2001
- 2001-03-21 US US09/813,133 patent/US6455294B1/en not_active Expired - Fee Related
-
2002
- 2002-03-19 WO PCT/US2002/008289 patent/WO2002077166A2/en not_active Application Discontinuation
- 2002-03-19 AU AU2002303137A patent/AU2002303137A1/en not_active Abandoned
- 2002-03-19 EP EP02731140A patent/EP1395674A4/en not_active Ceased
- 2002-03-19 CA CA002441115A patent/CA2441115A1/en not_active Abandoned
- 2002-08-07 US US10/212,877 patent/US6818429B2/en not_active Expired - Fee Related
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2004
- 2004-09-30 US US10/954,110 patent/US20050042670A1/en not_active Abandoned
-
2008
- 2008-07-16 US US12/218,759 patent/US20090082273A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2002077166A2 (en) | 2002-10-03 |
EP1395674A4 (en) | 2005-04-20 |
US6818429B2 (en) | 2004-11-16 |
US20050042670A1 (en) | 2005-02-24 |
EP1395674A2 (en) | 2004-03-10 |
AU2002303137A1 (en) | 2002-10-08 |
WO2002077166A3 (en) | 2003-12-11 |
US20090082273A1 (en) | 2009-03-26 |
CA2441115A1 (en) | 2002-10-03 |
US6455294B1 (en) | 2002-09-24 |
US20030017574A1 (en) | 2003-01-23 |
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