CA2309891A1 - Production of fibrinogen in transgenic animals - Google Patents

Abstract

Materials and methods for producing fibrinogen in transgenic non-human mammals are disclosed. DNA segments encoding A.alpha., B.beta. and .gamma. chains of fibrinogen are introduced into the germ line of a non-human mammal, and the mammal or its female progeny produces milk containing fibrinogen expressed from the introduced DNA
segments.
Non-human mammalian embryos and transgenic non-human mammals carrying DNA
segments encoding heterologous fibrinogen polypeptide chains are also disclosed.

Description

Description PRODUCTION OF FIBRINOGEN IN TRANSGENIC ANIMALS
Backcround of the Invention The final step in the blood coagulation cascade is the thrombin-catalyzed conversion of the soluble plasma protein fibrinogen to insoluble fibrin. Thrombin cleaves a small peptide (fibrinopeptide A) from one of the three component chains (the Aa-chain) of fibrinogen. Fibrin monomers subsequently polymerize and are cross-linked by activated factor XIII to form a stable clot.
Fibrinogen is a key component of biological tissue glues (see, e.g., U.S. Patents Nos. 4,377,572 and 4,442,655), which mimic the formation of natural blood clots to promote hemostasis and repair damaged tissue.
Tissue glues provide an adjuct or alternative to sutures, staples and other mechanical means for wound closure.
However, the principal ingredients of these products (fibrinogen, factor XIII and thrombin) are prepared from pooled human plasma by cryoprscipitation (e. g. U.s.
Patents No. 4,377,572; 4,362,567; 4,909,251) or ethanol precipitation (e. g. U.S. Patent No. 4,442,655) or from single donor plasma (e. g. U.S. Patent No. 4,627,879;
Spotnitz et al., Am. Sub ~: 166-168, 1989). The resultant fibrinogen/factor XIII preparation is mixed with bovine thrombin immediately before use to convert the fibrinogen to fibrin and activate the factor XIII, thus initiating coagulation of the adhesive.
Commercially available adhesives are of pooled plasma origin. Because blood-derived products have been associated with the transmission of human immunodeficiency virus (HIV), hepatitis virus and other etiologic agents, the acceptance and availability of such adhesives is limited. At present they are not approved for use in the United States.
While the use of autologous plasma reduces the risk of disease transmission, autologous adhesives can only be used in elective surgery when the patient is able to donate the necessary blood in advance.
As noted above, fibrinogen consists of three polypeptids chains, each of which is present in two copies in the assembled molecule. These chains, designated the Aa, B~,and y-chains, are coordinately expressed, assembled and secreted by the liver. While it might be expected that recombinant DNA technology could provide an alternative to the isolation of fibrinogen from plasma, this goal has proven to be elusive. The three fibrinogen chains have been individually expressed in E. coli (Lord, ~1 ~,: 33-38, 1985; Bolyard and Lord, Gene ~~: 183-192, 1988; Bolyard and Lord, ; lood ~: 1202-1206), but functional fibrinogen has not been produced in a prokaryotic system. Expression of biologically competent fibrinogen in yeast has not been reported. Cultured transfected mammalian cells have been used to express biologically active fibrinogen (Farrell et al., Blood 55a, 1989; Hartwig and Danishefsky, J. Biol. Chem. 266:
6578-6585, 1991; Farrell et al., Biochemistry ~Q: 9414-9420, 1991), but expression levels have been so low that production of recombinant fibrinogen in commercial quantities is not feasible. Experimental evidence suggests that lower transcription rates in cultured cells as compared to liver may be a factor in the low expression rates achieved to date, but increasing the amount of fibrinogen chain mRNA in transfected BHK cells did not produce corresponding increases in fibrinogen protein secretion (Drunkard and Foster, XIV Congress of the International Society on Thrombosis and Haemostasis, 1993). These latter results suggest that proper assembly and processing of fibrinogen involves tissue-specific mechanisms not present in common laboratory cell lines.

There remains a need in the art for methods of producing large quantities of high quality fibrinogen for use in tissue adhesives and other applications. There is a further need fot fibrinogen that is free of blood-borne pathogens. The present invention fulfills these needs and provides other, related advantages.
Summary of the Invention It is an aspect of the present invention to l0 provide commercially useful quantities of recombinant fibrinogen, particularly recombinant human fibrinogen. It is a further object of the invention to provide materials and methods for expressing fibrinogen in the mammary tissue of transgenic animals, particularly livestock animals such as cattle, sheep, pigs and goats.
Within one aspect, the present invention provides a method for producing fibrinogen comprising (a) providing a first DNA segment encoding a secretion signal operably linked to a fibrinogen Aa chain, a second DNA
segment encoding a secretion signal operably linked to a fibrinogen H~ chain, and a third DNA segment encoding a secretion signal operably linked to a (fibrinogen ~r chain, wherein each of the first, second and third segments is operably linked to additional DNA segments required for its expression in the mammary gland of a host female mammal; (b) introducing the DNA segments into a fert_lized egg of a non-human mammalian species; (c) inserting the egg into an oviduct or uterus of a female of the species to obtain offspring carrying the DNA constructs; (d) breeding the offspring to produce female progeny that express the first, second and third DNA segments and produce-milk containing biocompetent fibrinogen encoded by the segments; (e) collecting milk from the female progeny;
and (f) recovering the fibrinogen from the milk. Within one embodiment, the egg containing the introduced segments is cultured for a period of time prior to insertion.

Within another aspect, the invention provides a method of producing fibrinogen comprising the steps of (a) incorporating a first DNA segment encoding a secretion signal operably linked to an Aa chain of fibrinogen into a S-lactoglobulin gene to produce a first gene fusion; (b) incorporating a second DNA segment encoding a secretion signal operably linked to a H~ chain of fibrinogen into a ~-lactoglobulin gene to produce a second gene fusion; (c) incorporating a third DNA segment encoding a secretion signal operably linked to a y chain of fibrinogen into a ~-lactoglobulin gene to produce a third gene fusion; (d) introducing the first, second and third gene fusions into the germ line of a non-human mammal so that the DNA
segments are expressed in a mammary gland of the mammal or i~s female progeny and biocompetent fibrinogen is secreted into milk of the mammal or its female progeny; (e) obtaining milk from the mammal or its female progeny; and (f) recovering the fibrinogen from the milk. Within preferred embodiments, the mammal is a sheep, pig, goat or 2o bovine.
Within another aspect, the invention provides a method for producing ffibrinogen comprising the steps of (a) providing a transgenic female non-human mammal carrying in its germline heterologous DNA segments encoding Aa, 8~ and ~ chains of fibrinogen, wherein the DNA
segments are expressed in a mammary gland of the mammal and fibrinogen encoded by the DNA segments is secreted into milk of the mammal; (b) collecting milk from the mammal; and (c) recovering the fibrinogen from the milk.
Within another aspect, the invention provides a.
non-human mammalian embryo containing in its nucleus heterologous DNA segments encoding Aa, B~ and ~ chains of fibrinogen. Within a related aspect, the invention provides a transgenic non-human female mammal that produces recoverable amounts of human fibrinogen in its milk.

Within another aspect, the invention provides a method for producing a transgenic offspring of a mammal comprising the steps of (a) providing a first DNA segment encoding a fibrinogen Aa chain, a second DNA segment 5 encoding a fibrinogen B~B chain, and a third DNA segment encoding a fibrinogen y chain, wherein each of said first, second and third segments is operably linked to additional DNA segments required for its expression in a mammary gland of a host female mammal and secretion into milk of the host female mammal; (b) introducing the DNA segments into a fertilized egg of a mammal of a non-human species;
(c) inserting the egg into an oviduct or uterus of a female of the non-human species to obtain an offspring carrying the first, second and third DNA segments. In a related aspect, the invention provides non-human mammals produced according to this process.
Within an additional aspect, the invention provides a non-human mammal carrying its germline DNA
segments encoding heterologous Aa, H~ and ~ chains of 2o fibrinogen, wherein female progeny of the mammal express tho DNA segments in a mammary gland to produce biocompetent fibrinogen.
These and other aspects of the invention will become evident to the skilled practitioner upon reference to the following detailed description and the attached drawings.

Brief Descristi_on of the --------- Drawings a human Figure, 1 illustrates the subcloning of fibrinogen Aa chain DNA sequence.

Figure 2 is a partial restriction map of the vector Zem228. Symbols used era MT-1 p, mouse matallothionsin promoter;
SV4ot, SV4o tenainator;
and SV40p, SV40 promoter.

Figure 3 illustrates the subcloning of a human fibrinogen B~ chain DNA sequence.

Figure 4 illustrates the subcloning of a human fibrinogen ~ chain DNA
sequence.

Figure 5 is a partial restriction map of the vector Zsm219b. Symbols used are MT-1 p, mouse metallothionein pr omoter; hGHt, human growth hormone terminator; SV40p, SV40 promoter; DHFR, dihydrofolate reductass gene; and SV40t, SV40 terminator.

Detai_ied Descri&~ion of the Inventiow Prior to setting forth the invention in detail, 2o it will be helpful to define certain terms used herein:
As used herein, the term "biocompetent fibrinogen" is used to denote fibrinogen that polymerizes when treated with thrombin to form insoluble fibrin.
The term "egg" is used to denote an unfertilized ovum, a fertilized ovum prior to fusion of the pronuclei or an early stage embryo (fertilized ovum with fused pronuclei).
A "female mammal that produces milk containing biocompatent fibrinogen" is one that, following pregnancy and delivery, produces, during the lactation period, milk containing recoverable amounts of biocompstent fibrinogen.
Those skilled in the art will recognized that such animals will produce milk, and therefore the fibrinogen, discontinuously.
The term "progeny" is used in its usual sense to include children and descendants.

The term "heterologous" is used to denote genetic material originating from a different species than that into which it has been introduced, or a protein produced from such genetic material.
Within the present invention, transgenic animal technology is employed to produce fibrinogen within the mammary glands of a host female mammal. Expression in the mammary gland and subsequent secretion of the protein of interest into the milk overcomes many difficulties l0 encountered in isolating proteins from other sources.
Milk is readily collected, available in large quantities, and well characterized biochemically. Furthermore, the major milk proteins are present in milk at high concentrations (from about 1 to 15 g/1).
From a commercial point of view, it is clearly preferable to use as the host a species that has a large milk yield. While smaller animals such as mice and rats can be used (and are preferred at the proof-of-concept stage), within the present invention it is preferred to use livestock mammals including, but not limited to, pigs, goats, sheep and cattle. Sheep are particularly preferred due to such factors as the previous history of transgenesis in this species, milk yield, cost and the ready availability of equipment for collecting sheep milk.
See WO 88/00239 for a comparison of factors influencing the choice of host species. It is generally desirable to select a breed of host animal that has been bred for dairy use, such as East Friesland sheep, or to introduce dairy stock by breeding of the transgenic line at a later date.
In any event, animals of known, good health status should be used.
Fibrinogen produced according to the present invention may be human fibrinogen or f ibrinogen of a non-human animal. For medical uses, it is preferred to employ proteins native to the patient. The present invention thus provides fibrinogen for use in both human and veterinary medicine. Cloned DNA molecules encoding the component chains of human fibrinogen are disclosed by Rixon et al. (Biochem.
,~"~: 3237, 1983) , Chung et al.
(Biochem. ~: 3244, 1983), Chung et al. (Biochem.
3250, 1983), Chung et al. (Adv. Exn. Med. Biol ,~, : 3 9-48, 1990) and Chung et al. (Ann. NY Acad. Sci ~Q$. 449-456, 1983). Bovine fibrinogen clones are disclosed by Brown et al. (Nuc. Acids Res. ,~: 6397, 1989) and Chung et al. (Proc. Natl. Acad. Sci. USA ~: 1466-1470, 1981).
Other mammalian fibrinogen clones are disclosed by Murakawa et al. (Thromb. Haemost. ~"~: 351-360, 1993).
Representative sequences of human Aa, B~ and ~ chain genes are shown in SEQ ID NOS: 1, 3 and 5, respectively. Those skilled in the art will recognize that allelic variants of these sequences will exist;.that additional variants can be generated by amino acid substitution, deletion, or insertion; and that such variants are useful within the present invention. In general, it is preferred that any engineered variants comprise only a limited number of amino acid substitutions, deletions, or insertions, and 2o that any substitutions are conservative. Thus, it is preferred to produce fibrinogen chain polypeptides that are at least 90~, preferably at least 95~, and more preferably 99~ or more identical in sequence to the corresponding native chains. The term "y chain" is meant to include the alternatively spliced y' chain of fibrinogen (Chung et al., Biochem. ~: 4232-4236, 1984).
A human fir' chain amino acid sequence is shown in SEQ ID
NO: 6. The shorter y chain is produced by alternative splicing at nucleotides 9511 and 10054 of SEQ ID NO: 5, resulting in translation terminating after nucleotide 10065 of SEQ ID NO: 5. .
To obtain expression in the mammary gland, a transcription promoter from a milk protein gene is used.
Milk protein genes include those genes encoding caseins, beta-lactoglobulin (BLG), a-lactalbumin, and whey acidic protein. The beta-lactoglobulin promoter is preferred.
In the case of the ovine beta-lactoglobulin gene, a region of at least the proximal 406 by of 5' flanking sequence of the ovine HLG gene (contained within nucleotides 3844 to 4257 of SEQ ID' N0:7) will generally be used. Larger portions of the 5' flanking sequence, up to about 5 kbp, are preferred. A larger DNA segment encompassing the 5' flanking promoter region and the region encoding the 5' non-coding portion of the beta-lactoglobulin gene (contained within nucleotides 1 to 4257 of SEQ ID N0:7) is particularly preferred. Sae Whitelaw et al., Hiochem ,T.
l0 ~ø: 31-39, 1992. Similar fragments of promoter DNA from other species are also suitable.
Other regions of the beta-lactoglobulin gene may also be incorporated in constructs, as may genomic regions of the gene to be expressed. It is generally accepted in the art that constructs lacking introns, for example, express poorly in comparison with those that contain such DNA sequences (see Hrinster et al., Proc. Natl. Aced. Sci.
y,$~ ,$~: 836-840, 1988; Palmiter et al. , Proc. Natl. Aced.
Sci. USA ~: 478-482, 1991; Whitelaw et al., Transg!enic Res. ~: 3-13, 1991; WO 89/01343; WO 91/02318). In this regard, it is generally preferred, where possible, to use genomic sequences containing all or some of the native introns of a gene encoding the protein or polypeptide of interest. within certain embodiments of the invention, the further inclusion of at least some introns from the beta-lactoglobulin gene is preferred. One such region is a DNA segment which provides for intron splicing and RNA
polyadenylation from the 3' non-coding region of the ovine beta-lactoglobulin gene. When substituted for the natural 3' non-coding sequences of a gene, this ovine beta-lactoglobulin segment can both enhance and stabilize expression levels of the protein or polypeptide of interest. Within other embodiments, the region surrounding the initiation ATG of one or more of the fibrinogen sequences is replaced with corresponding sequences from a milk specific protein gene. Such replacement provides a putative tissue-specific initiation environment to enhance expression. It is convenient to replace the entire fibrinogen chain pre-pro and 5' non-coding sequences with those of, for example, the BLG gene, although smaller regions may be replaced.
5 For expression of fibrinogen, DNA segments encoding each of the three component polypeptide chains of fibrinogen are operably linked to additional DNA segments required for their expression to produce expression units.
Such additional segments include the above-mentioned milk to protein gene promoter, as well as sequences which provide for termination of transcription and polyadenylation of mRNA. The expression units will further include a DNA
segment encoding a secretion signal operably linked to the segment encoding the fibrinogen polypeptide chain. The secretion signal may be a native fibrinogen secretion signal or may be that of another protein, such as a milk protein. The term "secretion signal" is used herein to denote that portion of a protein that directs it through the secretory pathway of a call to the outside. Secretion signals are most commonly found at the amino-termini of proteins. See, for example, von Hainje, Nuc. Acids Res.
,: 4683-4690, 1986; and Meade et al., LT.S. Patent No.
4,873,316, Construction of expression units is conveniently carried out by inserting a fibrinogen chain sequence into a plasmid or phage vector containing the additional DNA
segments, although the expression unit may be constructed by essentially any sequence of ligations. It is particularly convenient to provide a vector containing a 3o DNA segment encoding a milk protein and to replace the coding sequence for the milk protein with that of a fibrinogen chain (including a secretion signal), thereby creating a gene fusion that includes the expression control sequences of the milk protein gene. In any event, cloning of the expression units in plasmids or other vectors facilitates the amplification of the fibrinogen sequences. Amplification is conveniently carried out in bacterial (e. g. E. coli) host cells, thus the vectors will typically include an origin of replication and a selectable marker functional in bacterial host cells.
In view of the size of the fibrinogen chain genes it is most practical to prepare three separate expression units, mix them, and introduce the mixture into the host. However, those skil7.ed in the art will recognize that other protocols may be followed. For example, expression units for the three chains can be introduced individually into different embryos to be combined later by breeding. In a third approach, the three expression units can be linked in a single suitable vector, such as a yeast artificial chromosome or phage P1 clone. Coding sequences for two or three chains can be combined in polycistronic expression units (see, e.g., Levinson et al., U.S. Patent No. 4,713,339).
The expression units) is(are) then introduced into fertilized eggs (including early-stage embryos) of the chosen host species. Introduction of heterologous DNA
can be accomplished by ons of several routes, including microinjection (e. g. U.S. Patent No. 4,873,191), retroviral infection (Jasnisch, Scie~y~g ~: 1468-1474, 1988) or site-directed integration using embryonic stem (ES) cells (reviewed by Bradley et al., Bio/Technolocv ~0:
534-539, 1992). The eggs are then implanted into the oviducts or uteri of pseudopregnant females and allowed to develop to term. Offspring carrying the introduced DNA in their germ line can pass the DNA on to their progeny in the normal, Mendelian fashion, allowing the development of transgenic herds. General procedures for producing transgenic animals are known in the art. see, for example, Hogan et al., ManiDUlati;p_v the Mouse Embrvo~ A
Laboratory Manual, Cold Spring Harbor Laboratory, 1986;
Simons et al., Bio~Technolocv ø: 179-183, 1988; Wall et al., Biol. ReDrod. ~,: 645-651, 1985; Buhler et al., Bio~ITechnoloav $: 140-143, 1990; Ebert et al. , Bio/Technolocrv ~: 835-838, 1991; Krimpenfort et al., Bio/Technolocrv ~: 844-847, 1991; Wall et al., J. Cell.
Biochem, g~: 1~3-120, 1992; and WIPO publications WO
88/00239, WO 90/05188, WO 92/11757; and GB 87/00458.
Techniques for introducing foreign DNA sequences into mammals and their germ cells were originally developed in the mouse. See, e.g., Gordon et al., Proc. Natl. Acad. Sci. USA

7384, 1980; Gordon and Ruddle, Science ~: 1244-1246, 1981; Palmiter and Hrinster, Cell ~: 343-345, 1985;
Brinster et al., proc. Natl. Acad. Sci. USA
4438-4442, 1985; and Hogan et al. (ibid.). These techniques were subsequently adapted for use with larger animals, including livestock species (see e.g., WIPO publications WO 88/00239, WO 90/05188, and WO 92/11757; and Simons et al., Hio/Technoloav ~,: 179-183, 1988). To summarize, in the most efficient route used to date in the generation of transgenic mice or livestock, several hundred linear molecules of the DNA of interest are injected into one of the pro-nuclei of a fertilized egg. Injection of DNA into the cytoplasm of a zygote can also be employed.
It is preferred to obtain a balanced expression of each fibrinogen chain to allow for efficient formation of the mature protein. Ideally, the three expression units should b~ on the same DNA molecule for introduction into eggs. This approach, however, may generate technical problems at, for example, the injection and manipulation stages. For example, the size of fibrinogen expression units may necessitate the use of yeast artificial chromosomes (YACs) or phage P1 to amplify and manipulate the DNA prior to injection. If this approach is followed, segments of DNA to be injected, containing all three expression units, would be very large, thus requiring modification of the injection procedure using, for example, larger bore needles. In a more simple approach, a mixture of each individual expression unit is used. It is preferred to combine equimolar amounts of the three expression units, although those skilled in the art will recognize that this ratio may be varied to compensate for the characteristics of a given expression unit. Some expression, generally a reduced level, will be obtained when lesser molar amounts of one or two chains are used, and expression efficiencies can generally be expected to decline in approximate proportion to the divergence from the preferred equimolar ratio. In any event, it is preferred to use a mixture having a ratio of Aa:B~:7 expression units~in the range of 0.5-1:0.5-1:0.5-1. When l0 the ratio is varied from equimolar, it is preferred to employ relatively more of the B~ expression unit.
Alternatively, one or a mixture of two of the expression units is introduced into individual eggs. However, animals derived by this approach will express only one or two fibrinogen chains. To generate an intact fibrinogen molecule by this approach requires a subsequent breeding program designed to combine all three expression units in individuals of a group of animals.
In general, female animals are superovulated by treatment with follicle stimulating hormone, then mated.
Fertilized eggs are collected, and the heterologous DNA is injected into the eggs using known methods. See, for example, U.S. Patent No. 4,873,191; Gordon et al., Proc.
Natl. Aced. Sci. USA ,~: 7380-7384, 1980; Gordon and Ruddle, ,~~,ence ~: 1244-1246, 1981; Palmiter and Brinster, Cell g,~: 343-345, 1985; Brinster et al., Proc.
Natl. Aced. Sci. USA $~: 4438-4442, 1985; Hogan et al., Mani_DUiatina the Mouse Embryo: A Laboratory Manual, Cold Spring Harbor Laboratory, 1986; Simons et al.
BioJTechnoloav g: 179-183, 1988; Wall et al., Biol.
Reprod. ~,: 645-651, 1985; Buhler et al., BiQ,~Technoloav $: 140-143, 1990; Ebert et al. , Bio/Technolow $: 835-838, 1991; Krimpenfort et al., Bio/Te~hnoloav ~,: 844-847, 1991;
Wall et al., ~. Cell. Biochem. ,4$: 113-120, 1992; WIPO
publications WO 88/00239, WO 90/05118, and WO 92/11757;
and GB 87/00458.

For injection into fertilized eggs, the expression units ,are removed from their respective vectors by digestion with appropriate restriction enzymes. For convenience, it is preferred to desigr the vectors so that the expression units are removed by cleavage with enzymes that do not cut either within the expression units or elsewhere in th~ vectors. The expression units are recovered by conventional methods, such as electro-elution followed by phenol extraction and ethanol precipitation, sucrose density gradient centrifugation, or combinations of these approaches.
DNA is injected into eggs essentially as described in Hogan et al., ibid. In a typical injection, eggs in a dish of an embryo culture medium are located using a stereo zoom microscope (x50 or x63 magnification preferred). Suitable media include Hepes (N-2-hydroxyethylpiperazina-N~-2-ethanesulphonic acid) or bicarbonate buffered media such as M2 or M16 (available from Sigma Chemical Co., St. Louis, USA) or synthetic oviduct medium (disclosed below). The eggs are secured and transferred to the center of a glass slide on an injection rig using, for example, a drummond pipette complete with capillary tube. Viewing at lower (e.g. x4) magnification is used at this stage. Using the holding pipette of the injection rig, the eggs are positioned centrally on the slide. Individual eggs are sequentially secured to the holding pipette for injection. For each injection process, th~ holding pipette/egg is positioned in the center of the viewing field. The injection needle 3o is than positioned directly below the egg. Preferably using x40 Nomarski objectives, both manipulator heights are adjusted to focus both the egg and the needle. The pronuclei are located by rotating the egg and adjusting the holding pipette assembly as necessary. Once the pronucleus has been located, the height of the manipulator is altered to focus the pronuclear membrane. The injection needle is positioned below the egg such that the needle tip is in a position below the center of the pronucleus. The position of the needle is then altered using the injection manipulator assembly to bring the needle and the pronucleus into the same focal plane. The 5 needle is moved, via the joy stick on the injection manipulator assembly, to a position to the right of the egg. With a short, continuous jabbing movement, the pronuclear membrane is pierced to leave the needle tip inside the pronucleus. Pressure is applied to the 10 injection needle via the glass syringe until the pronucleus swells to approximately twice its volume. At this point, the needle is slowly removed. Reverting to lower (e. g. x4) magnification, the injected egg is moved to a different area of the slide, and the process is 15 repeated with another egg.
After the DNA is injected, the eggs may be cultured to allow the pronuclei to fuse, producing one-cell or later stage embryos. In general, the eggs are cultured at approximately the body temperature of the species used in a buffered medium containing balanced salts and serum. Surviving embryos are than transferred to psaudopregnant recipient females, typically by inserting them into the oviduct or uterus, and allowed to develop to term. During embryogenesis, the injected DNA
integrates in a random fashion in the genomes of a small number of the developing embryos.
Potential transgenic offspring are screened via blood samples and/or tissue biopsies. DNA is prepared from these samples and examined for the presence of the 3o injected construct by techniques such as polymerise chain reaction (PCR; sea Mullis, U.S. Patent No. 4,683,202) and Southern blotting (Southern, J. Mol. Biol. x:503, 1975;
Maniatis et al., Molecular Cloninq: A Laborator~r Manual, Cold Spring Harbor Laboratory, 1982). Founder transgenic animals, or GOs, may be wholly transgenic, having transgenes in all of their cells, or mosaic, having transgenes in only a subset of cells (see, for example, Wilkie et al., DeveloB. Biol, ~; 9-18, 1986). In the latter case, groups. of germ cells may be wholly or partially transgenic. In the latter case, the number of transgenic progeny from a founder animal will be less than the expected 50~ predicted from Mendelian principles.
Founder GD animals era grown to sexual maturity and mated to obtain offspring, or Gis. The Gis are also examined for the presence of the transgene to demonstrate transmission from~foundsr GO animals. In the case of male GOs, these may be mated with several non-transgenic females to generate many offspring. This increases the chances of observing transgene transmission. Female GO
founders may be mated naturally, artificially inseminated or superovulated to obtain many eggs which are transferred to surrogate mothers. The latter course gives '-..he best chance of observing transmission in animals having a limited number of young. The above-described breeding procedures are used to obtain animals that can pass the DNA on to subsequent generations of offspring in the normal, Mendelian fashion, allowing the development of, for example, colonies (mice), flocks (sheep), or herds (pigs, goats and cattle) of transgenic animals.
The milk from lactating GO and G1 females is examined for the expression of the heterologous protein using immunological techniques such as ELISA (see Harlow and Lane, Antibodies. A Laboratory anu ]~~, Cold Spring Harbor Laboratory, 1988) and Western blotting (Towbin et al., Proc. Natl. Aced. Sci. USA ~: 4350-4354, 1979). For a variety of reasons known in the art, expression levels 0! the heterologous protein will be expected to differ between individuals.
A satisfactory family of animals should satisfy three criteria: they should be derived from the same founder GO animal; they should exhibit stable transmission of the transgene; and they should exhibit stable expression levels from generation to generation and from lactation to lactation of individual animals. These principles have been demonstrated and discussed (Carver et al., Hio/Techno~ow ~: 1263-1270, 1993). Animals from such a suitable family are referred to as a "line."
Initially, male animals, GO or G1, are used to derive a flock or herd of producer animals by natural or artificial insemination. In this way, many female animals containing the same transgene integration event can be quickly generated from which a supply of milk can be obtained.
The fibrinogen is recovered from milk using standard practices such as skimming, precipitation, filtration and protein chromatography techniques.
Fibrinogen produced according to the present invention is useful within human and veterinary medicine, such as in the formulation of surgical adhesives.
Adhesives of this type are known in the art. See, for example, U.S. Patents No. 4,377,572; 4,442,655; 4,462,567;
and 4,627,879, In general, fibrinogen and factor XIII are combined to form a first component that is mixed just prior to use with a second component containing thrombin. The thrombin converts the fibrinogen to fibrin, causing the mixture to gel, and activates the factor XIII. The activated factor XIII cross links the fibrin to strengthen and stabilize the adhesive matrix. Such adhesives typically contain from about 30 mg/ml to about 100 mg/ml fibrinogen and from about 50 ;tg/ml to about 500 ~tg/ml factor XIII. They may also contain additional ingredients, such as aprotinin, albumin, fibronectin, bulking agents, and solubilizers.
Methods far producing factor XIII are known in the art.
See, for example, U.S. Patent No. 5,204,447. The fibrinogen is also useful for coating surfaces of polymeric articles, e.g. synthetic vascular grafts, as disclosed in U.S. Patent No. 5,272,074.
The invention is further illustrated by the following non-limiting examples.

The multiple cloning site of the vector pUCl8 (Yanisch-Perron et al., Gene x:103-119, 1985) was removed and replaced with a synthetic double stranded oligonucleotide (the strands of which are shown in SEQ ID
NO: 8 and SEQ ID NO: 27) containing the restriction sites Pvu I/Mlu I/Eco ~RV/Xba I/Pw I/Mlu I, and flanked by 5~
overhangs compatible with the restriction sites Eco RI and Hind III. pUClB was cleaved with both Eco RI and Hind III, the 5~ terminal phosphate groups were removed with calf intestinal phophastase, and the oligonucleotide was ligated into the vector backbone. The DNA sequence across the junction was confirmed by sequencing, and the new plasmid was called pUCPM.
The ~-lactoglobulin (BLG) gene sequences from pSSitgXS (disclosed in WIPO publication WO 88/00239) were excised as a Sal I-Xba I fragment and recloned into the vector pUCPM that had been cut with Sal I and Xba I to construct vector pUCXS. pUCXS is thus a pUClB derivative containing the entire HLG gene from the sal I site to the Xba I site of phage SS1 (Ali and Clark, J. Mol. Biol.
415-426, 1988).
The plasmid pSSitgSE (disclosed in WIPO
publication WO 88/00239) contains a 1290 by BLG fragment flanked by Sph I and EcoR I restriction sites, a region spanning a unique Not I site and a single Pw II site which lies in the 5 ~ untranslated leader of the BLG mRNA.
Into this Pvu II site was ligated a double stranded, 8 by JNA linker (5~-GGATATCC-3~) encoding the recognition site for the enzyme Eco RV. This plasmid was called pSSitgSE/RV. DNA sequences bounded by Sph I and Not I
restriction sites in pSSitgSE/RV were excised by enzymatic digestion and used to replace the equivalent fragment in pUCXS. The resulting plasmid was called pUCXSRV. The sequence of the BLG insert in pUCSXRV is shown in SEQ ID

NO: 7, with the unique Eco RV site at nucleotide 4245 in the 5~ untranslated leader region of the BLG gene. This site allows insertion of any additional DNA sequences under the control of the BLG promoter 3' to the transcription initiation site.
Using the primers BLGAMP3 (5~-TGG ATC CCC TGC
CGG TGC CTC TGG-3' ; SEQ ID NO: 9 ) and BLGAMP4 ( 5 ~ -AAC GCG
TCA TCC TCT GTG AGC CAG-3'; SEQ ID NO: 10) a PCR fragment of approximately 650 by was produced from sequences immediately 3~ to the stop codon of the BLG gene in pUCXSRV. Tha PCR fragment was engineered to have a BamH I
site at its 5~ and and an Mlu I site at its 3~ end and was cloned as such into BamH I and Mlu I cut pGEM7zf(+) (Promega) to give pDAM200(+).
pUCXSRV was digested with Kpn I, and the largest, vector containing band was gel purified. This band contained the entire pUC plasmid sequences and some 3~ non-coding sequences from the BLG gene. Into this backbone was ligatad the small Kpn I fragment from pDAM200(+) which, in the correct orientation, effectively engineered a BamH I site at the extreme 5~ end of the 2.6 Kbp of the BLG 3~ flanking region. This plasmid was called pBLAC200. A 2.6 Kbp Cla I-Xba I fragment from p8LAC200 way ligatad into Cla I-Xba I cut pSP72 vector (Promaga), thus placing an EcoR V site immediately upstream of th~ BLG sequences. This plasmid was called pBLAC210.
Tha 2.6 Kbp Eco RV-Xba I fragment from p8LAC210 was ligatad into Eco RV-Xba I cut pUCXSRV to form pMAD6.
This, in aff.ct, excised all coding and intros sequences from pUCXSRV, forming a BLG minigane consisting of 4.3 Kbp of 5~ promoter and 2.6 Kbp of 3~ downstream sequences flanking a unique EcoR V site. An oligonucleotida linker (ZC6839: ACTACGTAGT; SEQ ID NO: 11) was inserted into the Eco RV site of pMAD6. This modification destroyed the Eco RV site and created a Sna BI site to be used for cloning purposes. The vector was designated pMAD6-Sna. Messenger RNA initiates upstream of the Sna HI site and terminates downstream of the Sna BI site. The precursor transcript will encode a single BLG-derived intros, intros 6, which is entirely within the 3' untranslated region of the gene.

Exam~rle II
Clones encoding the individual fibrinogen chains wars obtained from the laboratory of Dr. Earl W. Davie, 10 University of Washington, Seattle. A genomic fibrinogen Aa-chain clone (Chung et al., 1990, ibid.) was obtained from the plasmid BS4. This plasmid contains the Aa clone inserted into the Sal I and Ham HI sites of the vector pUCl8, but lacks the coding sequence for the first four 15 amino acids of the Aa chain. A genomic H~-chain DNA (Chung et al. , ibid. ) was isolated from a lambda Charon 4A phage clone (designated ~a4) as two EcoRI fragments of ca. 5.6 Kbp each. The two fragments wars cloned separately into pUCl9 that had been digested with Eco RI and treated with 20 calf intestinal phosphatass. The resulting clones were screened by digestion with the restriction enzyme Pvu II
to distinguish plasmids with the 5' and 3' B~ inserts (designated Beta5'RI/puc and Bsta3'RI/puc, respectively).
Genomic y-chain clones were isolated as described by Rixon et al. (Hiochemistrv ~q: 2077-2086, 1985). Clone py12A9 comprises 5' non-coding sequencss and approximately 4535 by of ~r-chain coding sequence. Clone p~r12F3 comprises the remaining coding sequence and 3' non-coding nucleotides.
Both are pBR322-based plasmids with the fibrinogen sequences inssrted at the EcoRI site. Thsss plasmids were used as templates for the respective PCR reactions.
The fibrinogen chain coding sequences were tailored for insertion into expression vectors using the polymerase chain reaction (PCR) as generally described by Mullis (U. S. Patent No. 4,683,202). This procedure removed native 5' and 3' untranslated sequences, added a 9 base sequence (CCT GCA GCC) upstream of the first ATG of each coding sequence, supplied the first four codons for the Aa-chain sequence, removed an internal Mlu I site in the Aa sequence ,and added restriction sites to facilitate subsequent cloning steps.
Referring to Figure 1, the 5~ end of the Aa coding sequence was tailored in a PCR reaction containing 20 pmola for each of primers ZC6632 (SEQ ID NO: 12) and ZC6627 (SEQ ID NO: 13), approximately 10 ng of plasmid BS4 template DNA, 10 ~ ~tl of a mix containing 2 . 5 mM each dNTP, l0 7.5 ~tl lOx Pyrococcus furiosus (Pfu) nNA polymerise buffer ,~l (200 mM Tris-HC1, pH 8.2, 100 mM KCl, 60 mM (NH4) 2504, 20 mM MgCl2, 1~ Triton X-100; 100 ;tg/ml nuclease free bovine serum albumin)(Stratagene, La Jolla, CA), and water to 75 ;tl. The mixture was heated to 94°C in a DNA thermal cyclar (Perkin-Elmer Corp., Norwalk, CT). To the heated mixture was added 25 ul of a mixture containing 2.5 ~tl lOx Pfu buffer ;1, 22 ;tl H20 and 1 ;tl 2.5 units/~tl Pfu DNA
polymerise (Stratagena). Ths reactions ware run in a DNA
thermal cycler (Perkin-Elmer) for five cycles of 94°, 45 seconds; 40°, 90 seconds; 72°, 120 seconds; 20 cycles of 94°, 45 seconds; 45°, 90 seconds; 72°, 120 seconds; then incubated at 72° for 7 minutes. The 5~ PCR-generated fragment was digested with Bam HI and Hind III, and the Sam HI-Hind III fragment was then ligated to an internal 2.91 Kbp Hind III-Xba I fragment and Bam HI, Xba I-digested pUCl8. PCR-generated axon sequences were sequenced.
Referring again to Figure 1, the 3~ end of the Aa coding sequence was tailored in a series of steps in which the Mlu I site 563 bases upstream from the stop codon of the Aa sequence was mutated using an overlap extension PCR reaction (Ho et al. , Gene ,~: 51-59, 1989) .
In the first reaction 40 pmols of each of primers ZC6521 (SEQ ID NO: 14) and ZC6520 (SEQ ID NO: 15) were combined with approximately 10 ng of plasmid BS4 template DNA in a reaction mixture as described above. The reaction was run for 5 cycles of 94°, 45 seconds; 40°, 60 seconds; 72°, Trade-mark seconds; 15 cycles of 94°, 45 seconds; 45°, 60 seconds;
72°, 120 seconds,~, then incubated at 72° for 7 minutes. A
second reaction was carried out in the same manner using 40 pmole of each of primers ZC6519 (SEQ ID NO: 16) and ZC6518 (SEQ ID NO: 17) and BS4 as template. The PCR-generated DNA fragments from the first and second reactions were isolated by gel electrophoresis and elution from the gel. Approximately 1/10 of each recovered reaction product was combined with 40 pmole of each of primers ZC6521 ( SEQ ID NO : 14 ) and ZC6518 ( SEQ ID NO: 17 ) in a PCR reaction in which the complementary 3' ends of each fragment (containing the single base change) annealed and served as a primer for the 3' extension of the complementary strand. PCR was carried out using the same reaction conditions as in the first and second 3' PCR
steps. The reaction product was then digested with Xba I
and Bam HI, and the Xba I-Ham HI fragmsnt was cloned into Xba I, Bam HI-digested pUCl8. PCR-generated exons were sequenced.
As shown in Figure l, the 5' Bam HI-Xba I
fragment (3.9 Kbp) and the 3' Xba I-Bam HI fragment (1.3 Kbp) were inserted into the Bam HI site of the vector Zem228. Zem228 is a pUCl8 derivative comprising a Bam HI
cloning site between a mouse MT-1 promoter and SV40 terminator, and a neomycin resistance marker flanked by Sv40 promoter and terminator sequences. See European Patent Office Publication EP 319,944 and Fig. 2. The entire Aa coding sequence was isolated from the Zem228 vec~~or as an Sna BI fragment, which was inserted into the Sna BI sits of the plasmid pMAD6-Sna.
Referring to Fig. 3, the 5' end of the Bp-chain was tailored by PCR using the oligonucleotides ZC6629 (SEQ
ID NO: 18) , ZC6630 (SEQ ID NO: 19) and ZC6625 (SEQ ID NO:
20). These primers were used in pairwise combinations (ZC6629 + ZC6625 or ZC6630 + ZC6625) to generate B~ coding sequences beginning at the first ATG codon (position 470 in SEQ ID NO: 3)(designated N1-Heta) or the third ATG

codon (position 512 in SEQ ID NO: 3)(designated N3-Beta).
Approximately 5, ng of Beta5~RI/puc template DNA was combined with 20 pmole of each of the primers (N1-Beta:ZC6629, SEQ ID NO: 18 + ZC6625, SEQ ID NO: 20; or N3-Bsta:ZC6630, SEQ ID NO: 19 + ZC6625, SEQ ID NO: 20) in a reaction mixture as described above. Ths mixtures ware incubated for 5 cycles of 94°, 45 seconds; 40°, 120 seconds; (N1-Bsta) or 90 seconds (N3-Beta); 72°, 120 seconds; 20 cycles of 94°, 45 seconds; 45°, 120 seconds;
(N1-Beta) or 90 seconds (N3-Beta); 72°, 120 seconds; then incubated at 72° for 7 minutes. The two reaction products N1, 555 by or N3, 510 bp) wars each digested with Eco RI
and Bgl II, and the fragments were ligated to the internal Bgl II-Xba I fragment and Eco RI + Xba I-digested pUCl9.
The 3~ end of the BQ sequence was tailored in a reaction mixture as described above using the oligonucleotide primers ZC6626 (SEQ ID NO: 21) and ZC6624 (SEQ ID NO: 22) and approximately 5 ng of Bsta3'RI/puc template. The mixtures ware incubated for 5 cycles of 94°, 45 seconds;
40°, 90 seconds; 72°, 120 seconds; 15 cycles of 94°, 45 seconds; 45°, 90 seconds; 72°, 120 seconds; than incubated at 72° for 7 minutes. A 990 by Bgl II-Eco RI fragment was isolated. This 3~ fragment was ligatsd to the adjacent coding fragment (340 bp, SphI-Hgl II) and Sph I + Eco RI-digested pUCl9. Tha 3~ and 5~ PCR-generated axons were sequenced. A third interansdiats vector was constructed by combining two internal fragments (4285 by Xba I-Eco RI and 383 kb Eco RI-Sph I) in Xba I + Sph I-digested pUCl9. The entire B~3 coding sequence (two forms) was then assembled by ligating one of the 5' Eco RI-Xba I fragments, the, internal Xba I-Sph I fragment, the 3' Sph I-Eco RI
fragment and Eco RI-digested vector pUCl9. The B~
sequence was then isolated as a 7.6 Kbp Sna BI fragment and inserted into the Sna BI site of pMAD6-Sna.
Referring to Fig. 4, the 5' end of the gamma chain sequence was tailored by PCR using the oligonucleotide primers ZC6514 (SEQ ID NO: 23) and ZC6517 (SEQ ID NO: 24) and approximately 50 ng of p~12A9 as template. The PCR reaction was run as described above using 40 pM of each primer. The reaction was run for 5 cycles of 94°, 45 seconds; 40°, 60 seconds, 72°, 120 seconds, followed by 15 cycles of 94°, 45 seconds; 45°, 60 seconds; 72°, 120 seconds. The resulting 213 by fragment was digested with Bam HI and Spe I, and the resulting restriction fragment was ligated with the adjacent downstream 4.4 kb Spe I-Eco RI fragment and Bam HI + Eco l0 RI digested pUCl9. The 3' end of the gamma chain sequence was tailored using oligonucleotide primera ZC6516 (SEQ ID
NO: 25) and ZC6515 (SEQ ID NO: 26) using 40 pM of each primer, approximately 50 ng of p~r12F3 template and the same thermal cycling schedule as used for the 5' fragment.
The resulting 500 by fragment was digested with Spe I and Bam HI, and the resulting restriction fragment was ligated with the upstream 2.77 kb Eco RI-Spe I fragment and Eco RI
+ Bam HI-digested pUCl9. All PCR-generated exons were sequenced. The entire y'-chain coding sequence was then assembled by ligating a 4.5 Kbp Bam HI-Eco RI 5' fragment, a 1.1 Kbp Eco RI-Pst I internal fragment and a 2.14 Kbp Pst I-Xba I 3' fragment in Bam HI + Xba I-digested Zem219b. Zem219b is a pUCl8-derived vector containing a mouse metallothionein promoter and a DHFR selectable marker operably linked to an SV40 promoter (Fig. 5).
Plasmid Zem219b has been deposited with American Type Culture Collection as an E. coli XL1-blue transformant under Accession No. 68979. The entire ~r~-chain coding sequence was then isolated as a 7.8 Kbp Sna B1 fragment and inserted into the Sna BI site of pMAD6-Sna.
Exam'! a III
Mice for initial breeding stocks (C57BL6J, CBACA) were obtained from Harlan Olac Ltd. (Hicester, UK).
These were mated in pairs to produce F1 hybrid cross (B6CBAF1) for recipient female, superovulated females, stud males and vasectomized males. All animals were kept on a 14 hour light/10 hour dark cycle and fed water and food (Special Diet Services RM3, Edinburgh, Scotland) ad libitum.
Transgc.-is mice were generated essentially as 5 described in Hogs; et al. , ManiDUlatinqy the Mouse Embrv~
A Laborato~y~ Manual, Cold Spring Harbor Laboratory, 1986, Female B6CBAF1 animals were supsrovulatad at 4-5 weeks of age by an i.p. infection of pregnant mares' .serum 10 gonadotrophin (FOLLIGOM"' Vet-Drug, Falkirk, Scotland) (5 iu) followed by an i.p. injection of human chorionic gonadotrophin (CHORULON; Vet-Drug, Falkirk, Scotland) (5 iu) 45 hours later. They were then mated with a stud male overnight. Such females were next examined for copulation 15 plugs. Those that had mated were sacrificed, and their eggs were collected for microinjection.
DNA was injected into the fertilized eggs as described in Hogan at al. (ibid.) Briefly, each of the vectors containing the Aa, Bp and y expression units was 20 digested with Mlu I, and the expression units were isolated by sucrose gradient centrifugation. All chemicals used ware reagent grads (Sigma Chemical Co., St.
Louis, MO, U.S.A.), and all solutions wars sterile and nuclease-Eras. Solutions of 20% and 40% sucrose in 1 M
25 NaCl, 20 mM Tris pH 8.0, 5 mM EDTA were prepared using UHP
water and filter sterilized. A 30% sucrose solution was prepared by mixing equal volumes of the 20% and 40%
solutions. A gradient was prepared by layering 0.5 ml steps of the 40%, 30% and 20% sucrose solutions into a 2 ml polyallomer tube and allowed to stand for one hour.
100 ~tl of DNA solution (max. 8 ~,cg DNA) was loaded onto the top of the gradient, and the gradient was centrifuged for 17-20 hours at 26,000 rpm, 15~C in a Beckman TL100 ultracentrifuge using a TLS-55 rotor (Beckman Instruments, Fullerton, CA, USA). Gradients were fractionated by puncturing the tube bottom with a 20 ga. needle and collecting drops in a 96 well microtiter plate. 3 ~tl # Trade-mark aliquots were analyzed on a 1% agarose mini-gel.
Fractions containing~the desired DNA fragment were pooled and ethanol precipitated overnight at -20°C in 0.3M sodium acetate. DNA pellets were resuspended in 50-100 ~l UHP
water and quantitated by fluorimstry. The expression units were diluted in~Dulbecco~s phosphate buffered saline without calcium and magnesium (containing, per liter, 0.2 g KCI, 0.2 g KH2P04, 8.0 g NaCl, 1.15 g Na2HP04), mixed (using either the~Ni-Beta or N3-Beta expression unit) in a 1:1:1 molar ratio, concentration adjuste3 to about 6 Etg/ml, and injected into the eggs (-2 pl total DNA
solution per egg).
Recipient females of b-8 weeks of age are prepared by mating 86CBAF1 females in natural estrus with vasectomized males. Females possessing copulation plugs are then kept for transfer of microinjected eggs.
Following birth of potential transgenic animals, tail biopsies ars taken, under anesthesia, at four weeks of age. Tissue samples are placed in 2 ml of tail buffer (0.3 M Na acetate, 50 mM HCl, 1.5 mM MgCl2, 10 mM Tris-HC1, pH 8.5, 0.5% NP40, 0.5% Tween ZO) containing 200 ;tg/ml proteinase K (Boehringer Mannheim, Mannheim, Germany) and vortexed. The samples are shaken (250 rpm) at 55°-60° for 3 hours to overnight. DNA prepared from biopsy samples is examined for the presence of the injected constructs by PCR and Southern blotting. The digested tissue is vigorously vortexed, and 5 ;tl aliquots are placed in 0.5 ml microcentrifuge tubes. Positive and negative tail samples are included as controls. Forty ;tl of silicone oil (HDH, Pools, UK) is added to each tube, and the tubes are briefly centrifuged. The tubes are incubated in the heating block of a thermal cycler (e. g.
Omni-gene, Hybaid, Teddington, UK) to 95°C for 10 minutes.
Following this, each tube has a 45 ~tl aliquot of PCR. mix added such that the final composition of each reaction mix is: 50 mM KCl; 2 mM MgCl2; 10 mM Tris-HC1 (pH 8.3) ; 0.01%
gelatin; 0.1% NP40, 10% DMSO; 500 nM each primer, 200 ~M

dN''Ps; 0.02 U/~l Taq polymerise (Boehringer Mannheim, Mannheim, Germany). The tubas are then cycled through 30 repeated temperature changes as required by the particular primers used. The primers may bs varied but in all cases must target the BLG promoter region. This is specific for the injected DNA fragments because the mouse doss not have a BLG gene. Twelve ~tl of 5x loading buffer containing Orange G marker dye (0.25 Orange G [Sigma] 15~ Ficoll type 400 [Pharmacia Biosystsms Ltd., Milton Keynes, UK]) is then added to each tubs, and the reaction mixtures are electrophoresad on a 1.6~ agarose gel containing ethidium bromide (Sigma) until the marker dye has migrated 2/3 of the length of the gel. Ths gel is visualized with a UV
light source emitting a wavelength of 254 nm. Transgenic mice having one or more of the injected DNA fragments are identified by this approach.
Positive tail samples are processed to obtain puts DNA. The DNA samples are screened by Southern blotting using a BLG promoter probe (nucleotides 2523-4253 of SEQ ID NO: 7). Specific cleavages with appropriate restriction enzymes (a.g. Eco RI) allow the distinction of the three constructs containing the Aa, 8S and y sequences.
Southern blot analysis of transgsnic mice prepared essentially as described above demonstrated that more than 50~ of progeny contained all three fibrinogen sequences. Examination of milk from positive animals by reducing SDS polyacrylamide gel electrophoresis demonstrated the presence of all three protein chains at concentrations up to 1 mg/ml. The amount of fully assembled fibrinogen was related to the ratios of individual subunits present in the milk. No apparent phenotype was associated with high concentrations of human fibrinogen in mouse milk.
Example IV
Donor ewes are treated with an intravaginal progesterone-impregnated sponge (CIiRONOGEST# Goat Sponge, Trade-mark Intervet, Cambridge, UK) on day 0. Sponges are left in situ for ten or twelve days.
Superowlation is induced by treatment of donor ewes with a total of one unit of ovine follicle stimulating hormone (OFSH) (OVAGEN; Horizon Animal Reproduction Technology Pty. Ltd., New Zealand) administered in eight intramuscular injections of 0.125 units per injection starting at 5:00 pm on day -4 and ending at 8:00 am on day 0. Donors are injected intramuscularly with 0.5 ml of a luteolytic agent (ESTRUMATE; Vet-Drug) on day -4 to cause regression of the corpus luteum, to allow return to estrus and owlation.
To synchronize owlation, the. donor animals are injected intramuscularly with 2 ml of a synthetic releasing hormone analog (RECEPTAL; Vet-Drug) at 5:00 pm on day 0.
Donors are starved of food and water for at least 12 hours before artificial insemination (A.I.). The animals are artificially inseminated by intrauterine laparoscopy under sedation and local anesthesia on day 1.
Either xylazine (ROMPUN; Vet-Drug) at a dose rate of 0.05-0.1 ml per 10 kg bodywaight or ACP injection 10 mg/ml (Vet-Drug) at a doss rate of 0.1 ml per 10 kg bodyweight is injected intramuscularly approximately fifteen minutes before A.I. to provide sedation. A.I. is carried out using freshly collected semen from a Poll Dorset ram.
Semen is diluted with equal parts of filtered phosphate buffered saline, and 0.2 ml of the diluted semen is injected per uterine horn. Immediately pre- or post-A. I., donors are given an intramuscular injection of AMOXYPEN #
(Vet-Drug).
Fertilized eggs are recovered on day 2 following starvation of donors of food and water from 5:00 pm on day 1. Recovery is carried out under general anesthesia induced by an intravenous injection of 5% thiopentone sodium (INTRAVAL SODIUM; Vet-Drug) at a dose rate of 3 ml per 10 kg bodyweight. Anesthesia is maintained by inhalation of 1-2% Halothane/02/N20 after intubation. To Trade-mark recover the fertilized eggs, a laparotomy incision is made, and the ,uterus is exteriorized. The eggs are recovered by retrograde flushing of the oviducts with Ovum Culture Medium (Advanced Protein Products, Brierly Hill, Wast Midlands, UR) supplemented with bovine serum albumin of Naw Zealand origin. After flushing, the uterus is returned to the abdomen, and the incision is closed.
Donors are allowed to recover post-operatively or are euthanized. Donors that are allowed to recover are given an intramuscular injection of Amoxypen L.A. a, the manufacturer's recommended dose rate immediately pre- or post-operatively.
Plasmids containing the three fibrinogen chain expression units are digested with Mlu I, and the expression unit fragments are recovered and purified on sucrose density gradients. The fragment concentrations are determined by lluorimetry and diluted in Dulbecco's phosphate bulfarad saline without calcium and magnesium as described above. Tha concentration is adjusted to 6 ~tg/ml and approximately 2 pl of the mixture is microinjected into one pronucleus o! each fertilized eggs with visible pronuclei.
All fertilized eggs surviving pronuclear microinjaction era cultured in vitro at 38.5°C in an atmosphere o! 5~ C02:5~ 02:90 N2 and about -100 humidity in a bicarbonate bu!lered synthetic oviduct medium (see Table) supplemented with 20~ v/v vasectomized ram serum.
Tha serum may be heat inactivated at 56°C !or 30 minutes and stored lrozan at -20°C prior to use. The fertilized eggs era cultured for a suitable period of time to allow early embryo mortality (caused by the manipulation techniques) to occur. These dead or arrested embryos are discarded. Embryos having developed to 5 or 6 cell divisions are transferred to synchronized recipient ewes.

Table Synthetic oviduct Medium 5 Stock A (Lasts '~ Mo nths) NaCl 6.29 g KCl 0.534 g ~2P04 0.162 g MgS04.7H O 0.182 g to Penicillin 0.06 g Sodium Lactate 60$ syrup 0.6 mls Super H20 99.4 mls Htock B (Lasts 2 we eks) 15 NaHC03 0.21 g Phenol red 0.001 g Super H20 10 mls Mock C (Lasts 2 we eks) 20 Sodium Pyruvate 0.051 g Super H20 10 mls Stock D (Lasts 3 mo nths) CaC12.2H20 0.262 g 25 Super H20 10 mls Stock E (Lasts 3 mo nths( Hepss 0.651 g Phenol red 0.001 g 30 Super H20 10 mls TQ make i lO
l f u~ B
m carbonate Buffered s o STOCK A 1 ml STOCK B 1 ml STOCK C 0.07 ml STOCK D 0.1 ml Super H20 7.83 ml Osmolarity should be 265-285 mOsm.

Add 2.5 ml of heat inactivated sheep serum and filter sterilize.

To make uo 10 mls o f HEPES Buffered Med STOCK A 1 ml STOCK 8 0.2 ml STOCK C 0.07 ml STOCK D 0.1 ml STOCK E 0.8 ml Super H20 7.83 ml Osmolarity should be 265-285 mOsm.
Add 2.5 ml of heat inactivated sheep serum and filter sterilize.
Recipient ewes are treated with an intravaginal progesterone-impregnated sponge (Chronogest Ewe Sponge or Chronogest Ewe-Lamb Sponge, Interest) left in situ for 10 or 12 days. The ewes are injected intramuscularly with 1.5 ml (300 iu) of a follicle stimulating hormone substitute (P.M.S.G., Interest) and with 0.5 ml of a luteolytic agent (Estrumate, Coopers Pitman-Moors) at sponge removal on day -1. The~ewes era tested for estrus with a vasectomized ram between 8:00 am and 5:00 pm on days 0 and 1.
Embryos surviving in vitro culture are returned to recipients ( starved from 5 : 00 pm on day 5 or 6 ) on day 6 or 7. Embryo transfer is carried out under general anesthesia as described above. The uterus is exteriorized via a laparotomy incision with or without laparoscopy.
Embryos are returned to one or both uterine horns only in ewes with at least ons suitable corpora lutea. After replacement of the uterus, the abdomen is closed, and the recipients are allowed to recover. The animals are given an intramuscular injection of Amoxypen L.A. at the manufacturer's recommended dose rate immediately pry- or post-operatively.
Lambs are identified by ear tags and left with their dams for rearing. Ewes and lambs are either housed and fed complete diet concentrates and other supplements and or ad lib. hay, or are let out to grass.
Within the (first week of life (or as soon thereafter as possible without prejudicing health), each lamb is tested for the presence of the heterologous DNA by two sampling procedures. A 10 ml blood sample is taken from the jugular vein into an EDTA vacutainer. If fit enough, the lambs also have a second 10 ml blood sample taken within one week of the first. Tissue samples are taken by tail biopsy as soon as possible after the tail has become desensitized after the application of a rubber elastrator ring to its proximal third (usually within 200 minutes after "tailing"). The tissue is placed immediately in a solution of tail buffer. Tail samples are kept at room temperature and analyzed on the day of collection. All lambs are given an intramuscular infection of Amoxypen L.A. at' the manufacturer's recommended dose rate immediately post-biopsy, and the cut end of the tail is sprayed with an antibiotic spray.
DNA is extracted from sheep blood by first separating white blood cells. A 10 ml sample of blood is diluted in 20 ml of Hank's buffered saline (HHS; obtained from Sigma Chemical Co. ) . Ten ml of the diluted blood is layered over 5 ml of Histopaque (Sigma) in each of two 15 ml screw-capped tubes. The tubes are centrifuged at 3000 rpm (2000 x g max.), low brake for 15 minutes at room temperature. White call interfaces are removed to a clean 15 ml tube and diluted to 15 ml in HBS. The diluted cells are spun at 3000 rpm for 10 minutes at room temperature, and the call pellet is recovered and resuspended in 2-5 ml of tail buffer.
To extract DNA from the white cells, 10% SDS is added to the resuspendsd cells to a final concentration of 1%, and the tube is inverted to mix the solution. One mg of fresh proteinase K solution is added, and the mixture is incubated overnight at 45°C. DNA is extracted using an equal volume of phenol/chloroform (x3) and chloroform/isoamyl alcohol (xi). Ths DNA is then precipitated by adding 0.1 volume of 3 M NaOAc and 2 volumes of ethanol, and the tubs is inverted to mix. The precipitated DNA is spooled out using a clean glass rod with a sealed end. The spool is washed in 70% ethanol, and the DNA is allowed to partially dry, then is redissolved in TE (10 mM Tris-HC1, 1 mM EDTA, pH 7.4).

DNA samples from blood and tail are analyzed by Southern blotting using probes for the BLG promoter region and the fibrinogen chain coding regions.
From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.

SEQUENCE LISTING
(1) GENERAL INFORMATION:
(i) APPLICANT: ZymoGenetics, Inc.
1201 Eastlake Avenue East Seattle, Washington 98102 United States of America Pharmaceutical Proteins Ltd.
Roslin Edinburgh Midlothian, Scotland EH25 9PP
(ii) TITLE OF INVENTION: Production of Fibrinogen in Transgenic Animals (iii) NUMBER OF SEQUENCES: 27 (iv) CORRESPONDENCE ADDRESS:
(A) ADDRESSEE: ZymoGenetics, Inc.
(B) STREET: 1201 Eastlake Avenue East (C) CITY: Seattle (D) STATE: WA
(E) COUNTRY: USA
(F) ZIP: 98102 (v) COMPUTER READABLE FORM:
(A) MEDIUM TYPE: Floppy disk (B) COMPUTER: IBM PC compatible (C) OPERATING SYSTEM: PC-DOS/MS-DOS
(D) SOFTWARE: PatentIn Release X1.0, Version X1.25 (vi) CURRENT APPLICATION DATA:
(A) APPLICATION NUMBER:
(B) FILING DATE:
(C) CLASSIFICATION:
(viii) ATTORNEY/AGENT INFORMATION;
(A) NAME: Parker, Gary E
(B) REGISTRATION NUMBER: 31-648 (C) REFERENCE/OOCKET NUMBER: 93-15PC
(ix) TELECOMMUNICATION INFORMATION:
(A) TELEPHONE: 206-442-6673 (B) TELEFAX: 206-442-6678 (2j INFORMATION FOR SEQ ID N0:1:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 5943 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (genomicj (viij IMMEDIATE SOURCE:
(B) CLONE: Human Fibrinogen A-alpha chain (ixj FEATURE:
(A) NAME/KEY: COS
(B) LOCATION: ~oin(31..84, 1154..1279, 1739..1922, 3055..3200, 3786..5210) (xij SEQUENCE DESCRIPTION: SEQ ID N0:1:

Met Phe Ser Met Arg Ile Val Cys Leu Val Leu Ser Val Val Gly Thr Ala Trp Thr Ala Asp Ser Gly Glu Gly Asp Phe Leu Ala Glu Gly Gly Gly Yal Arg Gly Pro Arg Val Val Glu Arg His Gln Ser Ala Cys Lys Asp Ser Asp Trp Pro Phe Cys Ser Asp Glu Asp Trp Asn Tyr LysCys ProSer GlyCysArg MetLys GlyLeuIle AspGlu YalAsn 65 . 70 75 GlnAsp PheThr AsnArgIle AsnLys LeuLysAsn SerLeu PheGlu TyrGln LysAsn AsnLysA_spSerHis SerLeuThr ThrAsn IleMet GTAAGTATTA

GluI1~ LeuArg GlyAspPhe SerSer AlaAsn AGCTACTTCA CGT
ATAACCATAT GAT
TTTCGATTTC AAT

Asn Arg Asp Asn ThrTyrAsnArg YalSer GluAspLeu ArgSerArg IleGlu Yal Leu LysArgLysVal IleGlu LysValGln HisIleGln LeuLeu Gln Lys AsnYalArgAla GlnLeu YalAspMet LysArgLeu Glu AAGGAAGGCG

ACTGAGTGTCTACTATATGCAGAGAAAAGTGTTATATCCaTCATCTACCTAAAAGTAGGT3330 GTG GAC
ATT GAT

Val Asp Ile Lys Ile Asp Ile Arg Ser Cys Arg Gly Ser Cys Ser Arg Ala Leu Ala Arg Glu Val GAT CTG AAG GAC TAT GAA~GAT CAG CAG AAG CAA CTT GAA CAG GTC ATT 3899 Asp Leu Lys Asp Tyr Glu Asp Gln Gln Lys Gln Leu Glu Gln Val Ile Ala Lys Asp Leu Leu Pro Ser Arg Asp Arg Gln His Leu Pro Leu Ile 210 215 22tr Lys Met Lys,Pro Yal Pro Asp Leu Yal Pro Gly Asn Phe Lys Ser Gln Leu Gln Lys Yal Pro Pro Glu Trp Lys Ala Leu Thr Asp Met Pro Gln Met Arg Met Glu Leu Glu Arg Pro Gly Gly Asn Glu Ile Thr Arg Gly Gly Ser Thr Ser Tyr G1y Thr Gly Ser Glu Thr Glu Ser Pro Arg Asn Pro Ser Ser Ala Gly Ser Trp Asn Ser Gly Ser Ser Gly Pro Gly Ser Thr Gly Asn Arg Asn Pro Gly Ser Ser Gly Thr Gly Gly Thr Ala Thr TGG AAA CCT GGG AGC TCT GGA CCT GGA AGT GCT GGA AGC TG~ AAC TCT 4283 Trp Lys Pro Gly Ser Ser Gly Pro Gly Ser Ala Gly Ser Trp Asn Ser Gly Ser Ser Gly Thr Gly Ser Thr Gly Asn Gln Asn Pro Gly Ser Pro Arg Pro Gly Ser Thr Gly Thr Trp Asn Pro Gly Ser Ser Glu Arg Gly Ser Ala Gly His Trp Thr Ser Glu Ser Ser Val Ser Gly Ser Thr Gly 370 375 ?80 GlnTrpHis SerGluSer GlySerPhe ArgPro AspSerPro GlySer GGGAACGvG AGGCCTAAC AAGCCAGAC TGGGGC ACATTTGAA GAGGTG 4523 GlyAsnAla ArgProAsn AsnProAsp TrpGly ThrPheGlu GluVal TCAGGAAAT,GTAAGTCCA GGGACAAGG AGAGAG TACCACACA GAAAAA 4571 SerGlyAsn YalSerPro GlyThrArg ArgGlu TyrHisThr GluLys LeuValThr SerLysGly AspLysGlu LeuArg ThrGlyLys GluLys Val Thr Ser Gly Ser Thr Thr Thr Thr Arg Arg Ser Cys Ser Lys Thr Yal Thr Lys Thr Yal Ile G1y Pro Asp Gly His Lys Glu Yal Thr Lys Glu Yal Val Thr Ser Glu Asp Gly Ser Asp Cys Pro Glu Ala Met Asp Leu Gly Thr Leu Ser Gly Ile Gly Thr Leu Asp Gly Phe Arg His Arg His Pro Asp Glu Ala Ala Phe Phe Asp Thr Ala Ser Thr Gly Lys Thr Phe Pro Gly Phe Phe Ser Pro Met Leu Gly Glu Phe Val Ser Glu Thr Glu Ser Arg Gly Ser Glu Ser Gly Ile Phe Thr Asn Thr Lys Glu Ser AGT TCT CAT CAC CCT GGG,ATA GCT GAA TTC CCT TCC CGT GGT AAA TCT 5003 Ser Ser His His Pro Gly Ile Ala Glu Phe Pro Ser Arg Gly Lys Ser Ser Ser Tyr Ser Lys Gln Phe Thr Ser Ser Thr Ser Tyr Asn Arg G1y Asp Ser Thr Phe Glu Ser Lys Ser Tyr Lys Met Ala Asp Glu Ala Gly Ser Glu Ala Asp His Glu Gly Thr His Ser Thr Lys Arg Gly His Ala lys Ser Arg Pro Val Arg Gly Ile His Thr Ser Pro leu Gly Lys Pro Ser Leu Ser Pro (2) INFORMATION FOR SEQ ID N0:2:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 644 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0:2:
Met Phe Ser Met Arg Ile Val Cys Leu Val Leu Ser Val Yal Gly Thr Ala Trp Thr Ala Asp Ser Gly Glu Gly Asp Phe Leu Ala Glu Gly Gly Gly Val Arg Gly Pro Arg Val Yal Glu Arg His Gln Ser Ala Cys Lys Asp Ser Asp Trp Pro Phe Cys Ser Asp Glu Asp Trp Asn Tyr Lys Cys Pro Ser Gly Cys Arg Met Lys Gly Leu Ile Asp Glu Val Asn Gln Asp Phe Thr Asn Arg Ile Asn Lys Leu Lys Asn Ser Leu Phe Glu Tyr Gln Lys Asn Asn Lys Asp Ser His Ser Leu Thr Thr Asn Ile Met Glu Ile Leu Arg Gly Asp Phe Ser Ser Ala Asn Asn Arg Asp Asn Thr Tyr Asn Arg Yal Ser Glu Asp Leu Arg Ser Arg Ile Glu Val Leu Lys Arg Lys Yal Ile Glu Lys Val Gln His Ile Gln Leu Leu Gln Lys Asn Yal Arg Ald Gln Leu Yal Asp Met Lys Arg Leu Glu Val Asp lle Asp Ile Lys Ile Arg Ser Cys Arg Gly Ser Cys Ser Arg Ala Leu Ala Arg Glu Val Asp Leu Lys Asp Tyr Glu Asp Gln Gln Lys Gln Leu Glu Gln Yal Ile Ala Lys Asp Leu Leu Pro Ser Arg Asp Arg Gln His Leu Pro Leu Ile Lys Met Lys Pro Yal Pro Asp Leu Val Pro Gly Asn Phe Lys Ser Gln Leu Gln Lys Val Pro Pro Glu Trp Lys Ala Leu Thr Asp Met Pro Gtn Met Arg Met Glu Leu Glu Arg Pro Gly Gly Asn Glu Ile Thr Arg Gly Gly Ser Thr Ser Tyr Gly 'fhr Gly Ser Glu Thr Glu Ser Pro Arg Asn Pro Ser Ser Ala Gly Ser Trp Asn Ser Gly Ser Ser Gly Pro Gly Ser Thr Gly Asn Arg Asn Pro Gly Ser Ser Gly Thr Gly Gly Thr Ala Thr Trp Lys Pro Gly Ser Ser Gly Pro Gly Ser Ala Gly Ser Trp Asn Ser Gly Ser Ser Gly Thr Gly Ser Thr Gly Asn Gln Asn Pro Gly Ser Pro Arg Pro Gly Ser Thr Gly Thr Trp Asn Pro Gly Ser Ser Glu Arg Gly Ser Ala Gly His Trp Thr Ser Glu Ser Ser Val Ser Gly Ser Thr Gly Gln Trp His Ser Glu Ser Gly Ser Phe Arg Pro Asp Ser Pro Gly Ser Gly Asn Ala Arg Pro Asn Asn Pro Asp Trp Gly Thr Phe Glu Glu Val Ser Gly Asn Val Ser Pro Giy Thr Arg Arg Glu Tyr His Thr Glu Lys Leu Val Thr Ser Lys Gly Asp Lys Glu Leu Arg Thr Gly Lys Glu Lys YalThr Ser Ser Thr Thr Thr Thr Arg Arg Ser Gly Cys Ser Lys Thr YalThr Lys Val Ile Gly Pro Asp Gly His Lys Thr 465Thr Glu Yal Lys GluVal Val Ser Glu Asp Gly Ser Asp Cys Pro Met Thr Glu Ala Asp LeuGly Thr Ser Gly Ile Gly Thr Leu Asp Gly His Leu Phe Arg Arg HisPro Asp Ala Ala Phe Phe Asp Thr Ala Ser Lys Glu Thr Gly Thr PhePro Gly Phe Ser Pro Met Leu Gly Glu Phe Glu Phe Val Ser Thr GluSer Arg Ser Glu Ser Gly Ire Phe Thr Asn Glu 545G1y Thr Lys Ser 550 . 555 SerSer His Pro Gly Ile Ala Glu Phe Pro Ser Lys His Arg Gly Ser SerSer Tyr Lys Gln Phe Thr Ser Ser Thr Ser Arg Ser Tyr Asn Gly AspSer Thr Glu Ser Lys Ser Tyr Lys Met Ala Ala Phe Asp Glu Gly SerGlu Ala His Asp His Ala Glu Gly Thr His Ser Thr Lys Arg Gly Lys Lys Ser Pro Arg Pro 640 Val Arg Gly Ile His Thr Ser Pro Leu Gly Ser Leu Ser Pro (2) INFORMATION FOR SEQ ID N0:3:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 8878 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear (iij MOLECULE TYPE: DNA (genomic) (vii) IMMEDIATE SOURCE:
(Bj CLONE: human fibrinogen B-beta chain ('ix) FEATURE:
(A) NAME/KEY: misc_RNA
(B) LOCATION: 1..469 (ix) FEATURE:
(A) NAME/KEY: exon (B) LOCATION: 470..583 (ixj FEATURE:
(Aj NAME/KEY: intron (B) LOCATION: 584..3257 (ixj FEATURE:
(A) NAME/KEY: exon (B) LOCATION: 3258..3449 (ix) FEATURE:
(Aj NAME/KEY: intron (Bj LOCATION: 3450..3938 (ixj FEATURE:
(Aj NAME/KEY: exon (B) LOCATION: 3939..4122 (ixj FEATURE:
(Aj NAME/KEY: intron (B) LOCATION: 4123..5042 (ix) FEATURE:
(Aj NAME/KEY: exon (B) LOCATION: 5043..5270 (ix) FEATURE:
(A) NAME/KEY: intros (B) LOCATION: 5271..5830 (ix) FEATURE: ' (A) NAME/KEY: exon (B) LOCATION: 5831..5944 (ix) FEATURE:
(A) NAME/KEY: intros (B) LOCATION: 5945..6632 (ix) FEATURE:
(A) NAME/KEY: exon (B) LOCATION: 6633..6758 (ix) FEATURE:
(A) NAME/KEY: intros (B) LOCATION: 6759..6966 (ix) FEATURE:
(A) NAME/KEY: exon (B) LOCATION: 6967..7252 (ix) FEATURE:
(A) NAME/KEY: intros (B) LOCATION: 7253..7870 (ix) FEATURE:
(A) NAME/KEY: axon (B) LOCATION: 7871..8102 (ix) FEATURE:
(A) NAME/KEY: 3'UTR
(8) LOCATION: 8103..8537 (ix) FEATURE:
(A) NAME/KEY: misc_RNA
(B) LOCATION: 8538..8878 (ix) FEATURE:
(A) NAME/KEY: CDS
(B) LOCATION: ~oin(470..583, 3258..3449, 3939..4122, 5043..5270, 5831..5944, 6633..6758, 6967..7252, 7871..8102) (xi) SEQUENCE DESCRIPTION: SEQ ID N0:3:

Met Lys Arg Met Yal Ser Trp Ser Phe His Lys Leu Lys Thr Met Lys His Leu Leu Leu Leu Leu Leu Cys Yal Phe Leu Val Lys Ser Gln Gly Val Asn Asp Asn Glu Glu TTCGGATCAT TAT~GAGTTT CAAGGGAACT TGAGTGTTGT ACTTATCAGA CTCTACATGT 1463 AC?TGCCCAA GGTCTCATAG CTGTAAGTCA ACCCTACGGT CAAGACCTAC AAGTAGCCGA c723 GTTACTGAAC AGTAAGCAAC CTACAGATTC ACTATCACCA ACCAGCCAGT T~aATGGATCT 3143 Gly Phe Phe Ser Ala Arg Gly His Arg Pro Leu Asp Lys Lys Arg Glu G1u Ala Pro Ser Leu Arg Pro Ala Pro Pro Pro Ile Ser Gly Gly Gly Tyr Arg Ala Arg Pro Ala Lys Ala Ala Ala Thr Gln Lys Lys Ilal Glu Arg Lys Ala Pro Asp Ala Gly Gly Cys Leu His Ala Asp Pra Asp Leu TTG TGT CAG TTG CAA
GAG GCT

Gly Val Leu Cys Pro Thr Gly Cys Gln Leu Gln Glu Ala GAA AGG CCA ATC
AGA AAT AGT

Leu Leu Gln Gln Val Asp Glu Leu Asn Glu Arg Pro Ile Arg Asn Ser GCT GTT TCC CAG
ACC TCC TCT

Asn Asn Val Glu Ser Ser Phe Gln Tyr Ala Val Ser Gln Thr Ser Ser AAA GAC CTG TGG G
CAA AAG AGG

Met Tyr Leu Leu Gln Lys Gln Val Lys Lys Asp Leu Trp Gln Lys Arg GTATGGTGGT TAGGATT' T GTTAATTTGT ATATGTCATG CGCCAAATCA TTTCCACTAA 4902 Asp Asn Glu Asn Val Val Asn Glu Tyr Ser Ser Glu Leu Glu Lys His Gln Leu Tyr Ile Asp Glu Thr Val Asn Ser AAT ATC CCA ACT AAC CTT CGT GTG CTT CGT TCA AiC CTG GAA AAC CTG 5167 Asn Ile Pro Thr Asn Leu Arg Val Leu Arg Ser Ile Leu Glu Asn Leu Arg Ser Lys Ile Gln Lys Leu Glu Ser Asp Yal Ser Ala Gln Met Glu Tyr Cys Arg Thr Pro Cys Thr Val Ser Cys Asn Ile Pro Val Yal Ser Gly Lys TGAAAATCTA ATATTTGTTA TATTATTTTC AAAGGTCTAT AATAA~ACAC TCCTTAGTAA 5740 CCTGAACATA ATGTTGTCTT~ACATTTGCAG AA TGT GAG GAA ATT ATC AGG AAA 5853 Glu Cys Glu Glu Ile Ile Arg Lys Gly Gly Glu Thr Ser Glu Met Tyr Leu Ile Gln Pro Asp Ser Ser Val Lys Pro Tyr Arg Val Tyr Cys Asp Met Asn Thr Glu Asn Gly Gly Trp Thr Val Ile Gln Asn Arg Gln Asp Gly Ser Val Asp Phe Gly Arg Lys Trp Asp Pro Tyr lys Gln Gly Phe Gly Asn Val Ala Thr Asn Thr Asp Gly Lys Asn Tyr Cys Gly Leu Pro GACAAAAATG TG~AAGCTAA AGATAAGGGA AGAAAGGCAG TTTTTAGTTT CCCA.4AATTT 6928 Gly Glu Tyr Trp Leu Gly Asn Asp Lys Ile Ser Gln Leu Thr Arg Met Gly Pro Thr Glu Leu Leu Ile Glu Met Glu Asp Trp Lys Gly Asp Lys Val Lys Ala His Tyr Gly Gly Phe Thr Val Gln Asn Glu Ala Asn Lys Tyr Gln Ile Ser Val AAC AAA TAC AGA GGA ACA GCC GGT AAT GCC CTC ATG GAT GG~i GCA TCT 7172 Asn Lys Tyr Arg Gly Thr Ala Gly Asn Ala Leu Met Asp Gly Ala Ser Gln Leu Met Gly Glu Asn Arg Thr Met Thr Ile His Asn Gly Met Phe 390 . 395 400 Phe Ser Thr Tyr Asp Arg Asp Asn Asp Gly Trp TAATCTGCAA AACGTAACTT,GACCACCGTA GTTCTGTTTC TAATAACGCC AAACACATTT 7862 Leu Thr Ser Asp Pro Arg Lys Gln Cys Ser Lys Glu Asp Gly Gly Gly Trp Trp Tyr Asn Arg Cys His Ala Ala Asn Pro Asn Gly AGA TAC TAC TGG GGT GGA CAG TAC ACC TGG GP.C ATG GCA AAG CAT GGC 8006 Arg Tyr Tyr Trp Gly Gly Gln Tyr Thr Trp Asp Met Ala Lys His Gly Thr Asp Asp Gly Yal Val Trp Met Asn Trp Lys Gly Ser Trp Tyr Ser ATG AGG AAG ATG AGT ATG AAG ATC AGG CCC TTC TTC CCA CAG CAA TAGTCCCCAA

Met Arg Lys Met Ser Met Lys Ile Arg Pro Phe Phe Pro Gln Gln TTCTTTCATA CATTATATTC CTCTAAAACT CTCAAGCAGA CGTGAGTGTo ACTTTTTGAA 8229 CACTTGTAAG.GAAGGAGAAG CGTTCACAAC CTCAAATAG: TAATAAACCG GTCTTGAATA 8649 ATGGTGhAAC CCCATCTCTA CTAAAAATAC AAAAATTAGC CAGGCGTGGT GGCAGGTGCC 8829 (2) INFORMATION FOR SEQ ID N0:4:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 491 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0:4:
Met Lys Arg Met Val Ser Trp Ser Phe His Lys Leu Lys Thr Met Lys His Leu Leu Leu Leu Leu Leu Cys Val Phe Leu Val Lys Ser Gln Gly Val Asn Asp Asn Glu Glu Gly Phe Phe Ser Ala Arg Gly His Arg Pro Leu Asp Lys Lys Arg Glu Glu Ala Pro Ser Leu Arg Pro Ala Pro Pro Pro Ile Ser Gly Gly Gly Tyr Arg Ala Arg Pro Ala Lys Ala Ala Ala Thr Gln Lys Lys Val Glu Arg Lys Ala Pro Asp Ala Gly Gly Cys Leu His Ala Asp Pro Asp Leu Gly Val Leu Cys Pro Thr Gly Cys Gln Leu Gln Glu Ala Leu Leu Gln Gln Glu Arg Pro Ile Arg Asn Ser Val Asp Glu Leu Asn Asn Asn Val Glu Ala Val Ser Gln Thr Ser Ser Ser Ser 130 ' 135 140 Phe Gln Tyr Met Tyr Leu Leu Lys Asp Leu Trp Gln Lys Arg Gln Lys Gln Val Lys Asp Asn Glu Asn Val Val Asn Glu Tyr Ser Ser Glu Leu Glu Lys His Gln Leu Tyr Ile Asp Glu Thr Val Asn Ser Asn Ile Pro Thr Asn Leu Arg Val Leu Arg Ser Ile Leu Glu Asn Leu Arg Ser Lys Ile Gln Lys Leu Glu Ser Asp Val Ser Ala Gln Met Glu Tyr Cys Arg Thr Pro Cys Thr Val Ser Cys Asn Ile Pro Val Val Ser Gly Lys Glu Cys Glu Glu Ile Ile Arg Lys Gly Gly Glu Thr Ser Glu Met Tyr Leu Ile Gln Pro Asp Ser Ser Val Lys Pro Tyr Arg Val Tyr Cys Asp Met Asn Thr Glu Asn Gly Gly Trp Thr Val Ile Gln Asn Arg Gln Asp Gly Ser Val Asp Phe Gly Arg Lys Trp Asp Pro Tyr Lys Gln Gly Phe Gly Asn Val Ala Thr Asn Thr Asp Gly Lys Asn Tyr Cys Gly Leu Pro Gly Glu Tyr Trp Leu Gly Asn Asp Lys Ile Ser Gln Leu Thr Arg Met Gly Pro Thr Glu Leu Leu Ile Glu Met Glu Asp Trp Lys Gly Asp Lys Val Lys Ala His Tyr Gly Gly Phe Thr Val Gln Asn Glu Ala Asn Lys Tyr Gln Ile Ser Val Asn Lys Tyr Arg Gly Thr Ala Gly Asn Ala Leu Met Asp Gly Ala Ser Gln Leu Met Gly Glu Asn Arg Thr Met Thr Ile His Asn Gly Met Phe Phe Ser Thr Tyr Asp Arg Asp Asn Asp Gly Trp Leu Thr Ser Asp Pro Arg Lys Gln Cys Ser Lys Glu Asp Gly Gly Gly Trp Trp Tyr Asn Arg Cys His Ala Ala Asn Pro Asn Gly Arg Tyr Tyr Trp Gly Gly Gln Tyr Thr Trp Asp Met Ala Lys His Gly Thr Asp Asp Gly Val Val Trp Met Asn Trp Lys Gly Ser Trp Tyr Ser Met Arg Lys Met Ser Met Lys Ile Arg Pro Phe Phe Pro Gln Gln (2) INFORMATION FOR SEQ ID N0:5:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 10564 base pairs (B) TYPE; nucleic acid (C) STRANDEONESS: double (D) TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (genomic) (vii) IMMEDIATE SOURCE:
(B) CLONE: human fibrinogen gamma chain (ix) FEATURE:
(A) NAME/KEY: COS
(B) LOCATION: join(1799..1876, 1973..2017, 2207..2390, 2510 ..2603, 4211..4341, 4645..4778, 5758..5942, 7426 ..7703, 9342..9571) (xi) SEQUENCE DESCRIPTION: SEQ ID N0:5:

AATTAAAGTA TTAGTATTTC TTTCAAACTG GAGGCATTTC TCCCACTAAC ATATTTCATC . 780 AAAACCTTGA

TTG CAC CCC CGG TTC
AAT TTA ATT

Met Ser Trp Ser Leu Tyr Tyr Ala Leu His Pro Arg Phe Asn Leu Ile Leu Leu Phe Leu Ser Ser Thr Cys Val Ala ATTT~TTCTC TTTTAG TAT GTT GCT ACC AGA GAC AAC TGC TGC ATC TTA 2005 Tyr Val Ala Thr Arg Asp Asn Cys Cys Ile Leu Asp Glu Arg Phe AGAGGGr,CAG AGGAATAGAA ATAATTCCCT CATAAATATC ATCTGGCACT TGTAACTTTT 2117 Gly Ser Tyr Cys Pro Thr Thr Cys Gly Ile Ala Asp Phe Leu Ser Thr Tyr Gln Thr Lys Val Asp Lys Asp Leu Gln Ser Leu Glu Asp Ile Leu His Gln Yal Glu Asn Lys Thr Ser Glu Yal Lys Gln Leu Ile Lys Ala Ile Gln Leu Thr Tyr Asn Pro Asp 61u Ser Ser Lys Pro Asn Met Ile Asp Ala Ala Thr Leu Lys Ser Arg Ile Met Leu Glu Glu Ile Met Lys Tyr Glu Ala Ser Ile Leu Thr His Asp Ser Ser Ile Arg AAGAAAGAT~ TTCTAGATGT CTTCAAATGC TAGTTTGACC ATATTTATCA AAAATTTTTT 2873 TGTAACCAGA AGCATTAAAG_AAGAAAGGGG AAGTATCTGT TGTTTTATTT TACATACAAT 3653 AAATATAAAA TTACTCTTCT GAAaGGAATA CTTATTTTTG TCTTCTTATT TTTGTTATCT 4193 Tyr Leu Gln Glu Ile Tyr Asn Ser Asn Asn Gln Lys Ile 11a1 Asn Leu Lys Glu Lys Ilal Ala Gln Leu Glu Ala Gln Cys Gln Glu Pro Cys lys Asp Thr Val Gln Ile His Asp Ile Thr Gly Lys TCAGTTGTCT_AGACCTTTCTTGAATAGCTA TTTAAAAGGAATGCTGATGT 4521 AAAAAAACAG

AATAGTTTAC

TGT CAA GCT AGC GGG
GAC ATT CTT
GCC AAT

Asp Cys Lys Gly Lys Gln Gln Asp Ala Ser Gly Ile Ala Leu Asn ATT AAA CAA GTC TAC
CCT CTG TGT
AAA GCT

Tyr Phe Asn Gln Phe leu Ile Lys Gln Val Tyr Pro Leu Cys Lys Ala ~

GAT GGG GTG AAG
TCT GGA
AAT GGA

Glu Ile Trp Thr Phe Gln Asp Gly Val Lys Ser Gly Asn Gly GGAACCTGTGTTGCATCTGCCACTTGCTGATACCCACTAG~GAATCTTGGCTCCTTTACTT 5318 A~g Asp Leu Phe Asp Lys Gly Lys Ser Asn Val GGA ACT

TrpIleGln TyrLysGlu GlyPhe His LeuSerPro Gly Thr Gly Thr AAG AGC

ThrGluPhe TrpLeuGly AsnGlu Ile HisLeuIle Thr Gln Lys Ser GTG TGG

SerAlaIle ProTyrAla LeuArg Glu LeuGluAsp Asn Gly Val Trp CCAACTTTTT
ATTGTAAAGA

ArgThrSer CCATTTCCCA.GCCACTGGAGATTAGAAAATAAGCTAAATATTTTCTGGAAATTTCTGTTC6762 ACT G TAT TTC AAG
GTG GGA
CCT GAA
G

Thr Ala Ala Met la Asp Asp Tyr Phe Lys Val Gly Pro Glu A

CGC TAT GCC GCT
TAC TTC
GCT GGT

lys Tyr Leu Thr Gly Asp Gly Asp Arg Tyr Ala Ala Tyr Phe Ala Gly AGT

AlaPheAsp GlyPhe AspPheGly AspAsp ProSerAsp LysPhe Phe ACATCCCAT AATGGC ATGCAGTTC AGTACC TGGGACAAT GaCAAT GAT 7612 ThrSerHis AsnGly MetGlnPhe SerThr TrpAspAsn AspAsn Asp LysPheGlu GlyAsn CysAlaGlu GlnAsp GlySerGly TrpTrp Met AsnLysCys HisAla GlyHisLeu AsnGly ValTyrTyr Gln ss AAGAAACTCT AAGG~AAAAT GCTTGATCTG TGTGACCCGG GGCGCCATGC CAGAGCTGTA 8783 GGAGATATTTTCAGTTAGCA ~GATAATACTATAAATTTTATGTAACTGGCAATGCACTTCG9263 TGTTTTAG

Gly GlyThrTyr Ser LysAlaSerThr ProAsn GlyTyrAsp AsnGlyIle IleTrpAla Thr TrpLysThrArg TrpTyr SerMetLys LysThrThr MetLysIle Ile ProPheAsnArg LeuThr IleGlyGlu GlyGlnGln HisHisLeu Gly GlyAlaLysGln ValArg ProGluHis ProAlaGlu ThrGluTyr Asp SerLeuTyrPro GluAsp GATTTGTAGAAAATTA CACAAAGTTT CHGAAATTCT

ACTGCTAACT
TCTATTGACC

AspLeu GTTACAAAGGAAATAGCAATTATGGCTTTTGCCCTCTAGGAGATA~AGGACAAATACAGG10461 CACAGCCAf,ACAACCAAGATGCATAGTATCCAAAGTGCAGCTG 10564 (2) INFORMATION FOR SEQ ID N0:6:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 453 amino acids (B) TYPE: amino acid (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID N0:6:
Met Ser Trp Ser Leu His Pro Arg Asn Leu Ile Leu Tyr Phe Tyr Ala Leu Leu Phe Leu Ser Ser Thr Cys Yal Ala Tyr Val Ala Thr Arg Asp Asn Cys Cys Ile Leu Asp Glu Arg Phe Gly Ser Tyr Cys Pro Thr Thr Cys Gly Ile Ala Asp Phe Leu Ser Thr Tyr Gln Thr Lys Val Asp Lys Asp Leu Gln Ser Leu Glu Asp Ile Leu His Gln Val Glu Asn Lys Thr Ser Glu Val Lys Gln Leu Ile Lys Ala Ile Gln Leu Thr Tyr Asn Pro Asp Glu Ser.Ser Lys Pro Asn Met Ile Asp Ala Ala~ Thr Leu Lys Ser Arg Ile Met Leu Glu Glu Ile Met Lys Tyr Glu Ala Ser Ile Leu Thr 115 v 120 125 His Asp Ser Ser Ile Arg Tyr Leu Gln Glu Ile Tyr Asn Ser Asn Asn Gln Lys I1e Val Asn Leu Lys Glu Lys Val Ala Gln Leu Glu Ala Gln Cys Gln Glu Pro Cys Lys Asp Thr Val Gln Ile His Asp Ile Thr Gly Lys Asp Cys Gln Asp Ile Ala Asn Lys Gly Ala Lys Gln Ser Gly Leu Tyr Phe Ile Lys Pro Leu Lys Ala Asn Gln Gln Phe Leu Yal Tyr Cys Glu Ile Asp Gly Ser Gly Asn Gly Trp Thr Val Phe Gln Lys Arg Leu Asp Gly Ser Val Asp Phe Lys Lys Asn Trp Ile Gln Tyr Lys Glu Gly Phe Gly His Leu Ser Pro Thr Gly Thr Thr Glu Phe Trp Leu Gly Asn Glu Lys Ile His Leu Ile Ser Thr Gln Ser Ala Ile Pro Tyr Ala Leu Arg Yal Glu Leu Glu Asp Trp Asn Gly Arg Thr Ser Thr Ala Asp Tyr Ala Met Phe Lys Yal Gly Pro Glu Ala Asp Lys Tyr Arg Leu Thr Tyr Ala Tyr Phe Ala Gly Gly Asp Ala Gly Asp Ala Phe Asp Gly Phe Asp Phe Gly Asp Asp Pro Ser Asp Lys Phe Phe Thr Ser His Asn Gly Met Gln Phe Ser Thr Trp Asp Asn Asp Asn Asp Lys Phe Glu Gly Asn Cys Ala Glu Gln Asp Gly Ser Gly Trp Trp Met Asn Lys Cys His Ala Gly His Leu Asn Gly 11a1 Tyr Tyr Gln Gly Gly Thr Tyr Ser Lys Ala Ser Thr Pro Asn Gly Tyr Asp Asn Gly Ile Ile Trp Ala Thr Trp Lys Thr Arg Trp Tyr Ser Met Lys Lys Thr Thr Met Lys Ile Ile Pro Phe Asn 405 . 410 415 Arg Leu Thr Ile Gly Glu Gly Gln Gln His His Leu Gly G?y Ala Lys Gln Ilal Arg Pro Glu His Pro Ala Glu Thr Glu Tyr Asp Ser Leu Tyr Pro Glu Asp Asp Leu (2) INFORMATION FOR SEQ ID N0:7:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 10807 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ovine beta-lactoglobulin (xi) SEQUENCE DESCRIPTION: SEQ ID N0:7:

TTCACATCTG TGAGCATGAT ATATTTTCCC CCTCTATATC ATCTTCfIATT CCTCCTATCA 360 GATAGCTCAT TGTTAGTGTA TATATAGAAA AGCAACAGAT TTC'.'ATGTAT TAATTTTGTA 540 CTCTCTCTGG ATGGTATTCT CTGGAAGCTG AAGGTTCCTG AAGTTP.TGAA TAGCTTTGCC 2160 CTCAGTCTAG TCTCTGCCTC CGTGiTCACA CGCCTTCTCC CCATGTCCCC TCCGTGTCCC 2640 G

AAGTGCCTCCTGCTTGCCCTGGGCCTGGCCCTCGCCTGTGGCGTCCAGGCCATCATCGTC 4320.

ACCCAGACCATGAAAGGCCTGGACATCCAGAAGGTTCGAGGGTTGGCCGGGTGGG~GAGT 4380 CATCAGGCCC TGGGG~CCCC CCTGTGAGAA TGGCTGGAAG CTGGGGTCCC TCCTGGCGAC 8460 GGGGGACTAG_~AGGGACCAG GACTGCAGTCACCCTTCCTGGGACCCAGGCCCCTCCAGGC8820 ACTCGGCAGAGA~ATCTGCCAGTTCACTTGGAGTGTTCAGTCAACACCCAAACT~GACAA9120 GTACCCAAACGCA~TGATCTGTCTGGCTAATGATGAGAGATTCCCAGTAGAGAGCTGGCA9300 CTGATGTGAAGAGCTGACTCATTTGAAAA~ACCCTGATGCTGGGAAAGATTGAGGGCAGG9480 TATTGGCAGGTGGATTCTTTACCACTGTGCCACCAGGGAAGCCCGTGTTACTCTCTATGT9960.

(2) INFORMATION FOR SEQ ID N0:8:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 47 base pairs (B) TYPE: nucleic acid (C) STRANDEONESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID N0:8:

(2) INFORMATION FOR SEQ ID N0:9:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 24 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: BLGAMP3 (xi)~SEQUENCE DESCRIPTION: SEQ ID N0:9:

(2) INFORMATION FOR SEQ ID N0:10:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 24 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: BLGAMP4 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:10:

(2) INFORMATION FOR SEQ IO N0:11:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 10 base pairs (B) TYPE: nucleic acid (C) STRANOEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLUNE: ZC6B39 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:11:

(2) INFORMATION FOR SEQ IO N0:12:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 42 base pairs (B) TYPE: nucleic acid (C) STRANOEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6632 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:12:
CGACGCGGAT CCTACGTAi,C TGCAGCCATG TTTTCCATGA GG 42 (2) INFORMATION FOR SEQ ID N0:13:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 21 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6627 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:13:

(2) INFORMATION FOR SEQ ID N0:14:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 24 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6521 (xi) SEQUENCE DESCRIPTION: SEQ IO N0:14:

(2) INFORMATION FOR SEQ ID N0:15:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 30 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6520 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:15:
GCATGAACf;T CGCGTGGTGG TTGTGCTACC 30 (2) INFORMATION FOR SEQ ID N0:16:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 30 ba:,e pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(8) CLONE: ZC6519 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:16:

(2) INFORMATION FOR SEQ ID N0:17:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 36 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6518 (xi) SEQUENCE DESCQIPTION: SEQ ID N0:17:

(2) INFORMATION FOR SEQ ID N0:18:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 45 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6629 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:18:

(2) INFORMATION FOR SEQ ID N0:19:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 45 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (fl) TOPOLOGY: linear (vii) IMMEDIATE aOURCE:
(8) CLONE: ZC6630 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:19:

(2) INFORMATION FOR SEQ ID N0:20:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 21 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vi i ) IdhIEDIATE SOURCE:
(B) CLONE: ZC6625 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:20:

(2) INFORMATION FOR SEQ ID N0:21:
(i) SEQUENCE i,HARACTERISTICS:
(A) LENGTH: 21 base pairs (B) TYPE: nucleic acid (C) STRANOEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6626 xi) SEQUENCE DESCpIPTION: SEQ ID N0:21:
:~.:...: iTACT GTGGCCTACC A 21 (2) INFORMATION FOR SEQ ID N0:22:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 33 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(6) CLONE: ZC6624 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:22:

(2) INFORMATION FOR SEQ ID N0:23:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 45 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6514 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:23:

(2) INFORMATION FOR SEQ ID N0:24:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 21 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6517 (xi) SEQUENCE DESCRIPTION: SEQ IO N0:24:

(2) INFORMATION FOR SEQ ID N0:25:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 22 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6516 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:25:

(2) INFORMATION FOR SEQ ID N0:26:

(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 22 base pairs (B) TYPE: nucleic acid (C) STRANOEDNESS: single (D) TOPOLOGY: linear (vii) IMMEDIATE SOURCE:
(B) CLONE: ZC6515 (xi) SEQUENCE DESCRIPTION: SEQ ID N0:26:

(2) INFORMATION FOR SEQ ID N0:27:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 47 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (xi) SEQUENCE DESCRIPTION: SEQ ID N0:27:
AAGCTACGCG TCGATCGTCT AGAGTATATC GTCGACGCGT CGATCGG

Claims (9)

1. A non-human mammalian embryo containing in its nucleus heterologous DNA segments encoding A.alpha., B.beta. and .gamma.
chains of fibrinogen.

2. A transgenic non-human female mammal that produces recoverable amounts of biocompetent human fibrinogen in its milk

3. A non-human mammal produced according to the process comprising, providing a first DNA segment encoding a fibrinogen A.alpha. chain, a second DNA segment encoding a fibrinogen B.beta. chain, and a third segment encoding a fibrinogen .gamma. chain, wherein each of said first, second and third segments is operably linked to additional DNA segments required for its expression in a mammary gland of a host female mammal and secretion into milk of said howst femaile maammal;
introducing said DNA segments into a fertilized egg of a mammal of a non-human species;
inserting said egg into an oviduct or uterus of a female of said non-human species to obtain an offspring carrying said first, second and third DNA segments.

4. A non-human mammal according to claim 3 wherein said mammal is female.

5. A female mammal according to claim 4 that produces milk containing biocompetent fibrinogen encoded by said DNA segments.

6. A non-human mammal according to claim 3 wherein said mammal is male.

7. A non-human mammal carrying in its germline DNA segments encoding heterologous heterologous DNA segments encoding A.alpha., B.beta. and .gamma. chains of fibrinogen, wherein female progeny of said mammal express said DNA segments in a mammary gland to produce biocompetent fibrinogen.

8. A mammal according to claim 7 wherein said mammal is female.

9. A mammal according to claim 7 wherein said mammal is male.