CN109777811A - Tomato SlMYB0 gene and its application in raising plant frigostabile - Google Patents
Tomato SlMYB0 gene and its application in raising plant frigostabile Download PDFInfo
- Publication number
- CN109777811A CN109777811A CN201910094106.5A CN201910094106A CN109777811A CN 109777811 A CN109777811 A CN 109777811A CN 201910094106 A CN201910094106 A CN 201910094106A CN 109777811 A CN109777811 A CN 109777811A
- Authority
- CN
- China
- Prior art keywords
- gene
- tomato
- slmyb0
- nucleotide sequence
- seq
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Peptides Or Proteins (AREA)
Abstract
It is 756bp that the invention discloses tomato SlMYB0 genes improving the application in plant frigostabile ability, the nucleotide sequence length of the gene SlMYB0, and sequence is SEQ ID NO:1, and corresponding amino acid sequence is as shown in SEQ ID NO:2.Tomato SlMYB0 is constructed by gene means and is overexpressed plant and gene knockout plant, regulates and controls the expression of the gene SlMYB0 to study its regulatory mechanism to tomato low-temperature resistance.As a result, it has been found that SlMYB0 is overexpressed the expression that can induce tomato low-temperature resistance gene under low temperature, the low-temperature resistance of tomato is improved.The present invention provides genetic resources to cultivate low temperature resistant New Tomato Variety, has preferable potential using value, to study the mechanism of tomato plants response adverse circumstance signal and the molecule mechanism based theoretical of tolerance adverse environment.
Description
Technical field
The present invention relates to the fields such as genetic engineering, molecular biology and physiology, specifically, being related to tomato SlMYB0 base
Clone, transgene carrier building and the conversion of tomato of cause more particularly to SlMYB0 gene are in improving plant frigostabile ability
Application.
Background technique
Tomato is the annual or herbaceos perennial in Solanaceae Solanum, and alias tomato, tomato are world wides
It is interior to cultivate most wide, the maximum vegetable crop of consumption figure.Tomato variety type is abundant, can not only eat raw and make vegetables but also can make fruit, kind
Lycopene ingredient in eggplant can prevent various cancers, be one of most popular healthy food in the world.Tomato is in facilities vegetable
In occupy an important position, therefore improve tomato reply poor environment ability, cultivate resistant variety have important actual production
Meaning.
In recent years, with the extreme variation of global climate, low temperature, which increasingly becomes a kind of, influences extensive abiotic stress,
Normal growth and agricultural production to plant cause great destruction.Therefore, the physiology for studying plant responding Chilling stress is raw
Change variation and molecule mechanism, find the key gene of regulation plant low temperature response, provides weight to obtain the acquisition of low temperature resistant plant
The theories integration wanted, to improve vegetables yield, quality and economic benefit, and ensure vegetables stable market supply all have it is very heavy
The science and realistic meaning wanted.
Myb transcription factor takes part in as one kind transcription factor maximum in plant including cell cycle, physiological metabolism
Many vital movements including balance and environment response etc..With finding that the quantity of myb gene increases sharply in plant, MYB turns
The information such as the determination of regulatory mechanism, gene expression profile and target gene of the factor are recorded also to enrich constantly.Have now been found that multiple MYB
The response of transcription factor participation plants against abiotic stress.In drought stress, most of myb transcription factor is related to ABA,
Drought stress response is participated in as there are 43 genes to be induced in 156 myb transcription factors of soybean by ABA.It is some in addition to drought stress
Myb transcription factor also assists in the Resistant process of plant.The TaPIMP1 of wheat, AtMYB46, AtMYB72 of arabidopsis,
AtMYB73 respectively can the invasion to pinta bacterium, ash arrhizus bacteria, root-rot from compacted spore bacterium make response adjusting;Arabidopsis AtMYB102/
AtM4 and AtMYB41 can be by causing dehydration to resist the invasion of extraneous pest after by insect bite, and arabidopsis AtMYB96 passes through
Regulate and control salicylic acid route of synthesis and improves disease resistance.In addition, arabidopsis AtMYB30 passes through very-long-chain fatty acid route of synthesis,
The infringement of plants by phytopathogenic bacterium, which generates in hypersensitivity reaction process, plays positive control.These illustrate that myb transcription factor participates in planting
Object is to the answering of environment stress, however effect and its regulatory mechanism of the tomato myb transcription factor in low temperature stress are fresh
It appears in the newspapers.Therefore, the tomato material of variable expression SlMYB0 is cultivated by the clone to SlMYB0 gene, transgenic technology,
In terms of improving tomato to the resistance of low temperature stress and excavation environment stress genetic resources, have a good application prospect.
Summary of the invention
The technical problem to be solved in the present invention is to provide gene SlMYB0 to improve the application in tomato low temperature tolerance ability.
In order to achieve the object of the present invention, gene SlMYB0 provided by the invention is improving answering in tomato low temperature tolerance ability
With the nucleotide sequence of the gene SlMYB0cDNA are as follows:
1) nucleotide sequence shown in SEQ ID NO:1;Or
2) nucleotide sequence shown in SEQ ID NO:1 is substituted, lacks and/or increases one or more nucleotide and tool
There is the nucleotide sequence of identical function;Or
3) hybridize under strict conditions with sequence shown in SEQ ID NO:1 and nucleotide sequence with the same function;Or
4) there is 90% or more homology and nucleotides sequence with the same function with nucleotide sequence 1), 2) or 3)
Column.
Invention also provides a kind of protein of said gene coding, which has shown in SEQ ID NO:2
Amino acid sequence.It should be appreciated that those skilled in the art can disclosed amino acid sequence according to the present invention, do not influencing its work
Under the premise of property, replaces, lacks and/or increase one or several amino acid, obtain the mutant nucleotide sequence of the albumen.It should be understood that
In view of the degeneracy of codon and the preferences of different plant species codon, those skilled in the art be can according to need using suitable
Close the codon of particular species expression.
The present invention also provides cloning vectors or all kinds of tables containing the low temperature resistant SlMYB0 gene order of tomato or its segment
Up to carrier, the host cell containing the carrier, the conversion plant cell containing the gene order or its specific fragment and turn
Gene plant.
Plant of the present invention is tomato.The low temperature resistant SlMYB0 gene of tomato is overexpressed in tomato and is compiled using gene
The technology of collecting is mutated, and foreign gene can be guided to be overexpressed in plant and gene editing knockout technology including the use of any
Carrier carry out.
The present invention also provides a kind of method for constructing low temperature resistant transgene tomato, including gene overexpression, the methods
Specifically: tomato total serum IgE is extracted, reverse transcription obtains cDNA, and using cDNA as template, F and R are primer, expand SlMYB0 gene, will
Amplified production is building up on plant over-express vector;Utilize CRISPR-P website design SlMYB0 gene target sequence, the target of synthesis
The Bbs I site of AtU6-sgRNA-AtUBQ-Cas9 carrier, the AtU6- that then will newly obtain are connected to after sequence anneals
SgRNA-AtUBQ-Cas9 segment is connected to the Hind III/Kpn I site of pCAMBIA1301 carrier, constructs tomato
SlMYB0 gene C RISPR expression vector.Then Agrobacterium is converted with the recombinant expression carrier obtained, then with the agriculture bar of conversion
Bacterium invades tomato cotyledon, and carries out Plant Tissue Breeding, screens positive transgenic tomato plant, obtains low temperature resistant transgenosis kind
Eggplant.Wherein, the nucleotide sequence of the primers F and R are as shown in SEQ ID NO:3 and 4.The nucleotide sequence of the sgRNA is such as
Shown in SEQ IN NO:5.
The plant expression vector that the present invention uses is the expression vector with 35S promoter, such as carrier pFGC1008-HA
Or pCAMBIA1301.
The present invention goes back while providing a kind of host cell, which is Bacillus coli cells, agrobatcerium cell.Its
In, the preferably described Agrobacterium is GV3101.
The present invention goes back while providing the purposes of said gene: for constructing transgene tomato, the transgene tomato energy
Enough resistances improved to low temperature stress.It, can be to used load for the ease of being identified Transgenic Tomato Plants and being screened
Body is processed, such as plant alternative label or resistant antibiotic marker is added.Overexpression noted earlier carries
It joined 3HA label protein in body pFGC1008.
The present invention constructs the transgenic plant of tomato SlMYB0 gene overexpression and gene knockout for the first time, and carries out function
Research.It is tested by low-temperature treatment, discovery SlMYB0 gene plays the role of positive regulation in the low temperature resistant stress of tomato.
SlMYB0 gene provided by the invention provides genetic resources to cultivate low temperature resistant New Tomato Variety, has preferable
Potential using value establishes theory for the mechanism for studying tomato plants response adverse circumstance signal and the molecule mechanism for being resistant to adverse environment
Basis.
Detailed description of the invention
To make the objectives, technical solutions, and advantages of the present invention clearer, with reference to the accompanying drawing to of the invention specific
Embodiment is described in further detail.
Fig. 1 is the vegetable protein Western Blot inspection of SlMYB0 gene overexpression tomato strain in the embodiment of the present invention 3
Survey result.
Fig. 2 is the sequencing result of the sgRNA sequence of SlMYB0 gene knockout tomato strain in the embodiment of the present invention 3.
Fig. 3 be in the embodiment of the present invention 4 under room temperature and cryogenic conditions and its result of protein content;Wherein, A is
The expression of SlMYB0 gene, B are the level of SlMYB0 protein content.
Fig. 4 is transgene tomato OE#16 and OE#18, myb0#13 in the embodiment of the present invention 4 under room temperature and cryogenic conditions
Low temperature resistant phenotype is showed with myb0#14.
Fig. 5 is transgene tomato OE#16 and OE#18, myb0#13 in the embodiment of the present invention 4 under room temperature and cryogenic conditions
With the conductivity variations of myb0#14.
Fig. 6 is transgene tomato OE#16 and OE#18, myb0#13 in the embodiment of the present invention 4 under room temperature and cryogenic conditions
Change with the PSII maximum Photochemical quantum yield (Fv/Fm) of myb0#14.
Fig. 7 is transgene tomato OE#16 and OE#18, myb0#13 in the embodiment of the present invention 4 under room temperature and cryogenic conditions
With the variation for resisting cold gene expression dose in myb0#14;Wherein, A is the expression of tomato CBF1 gene, and B is tomato CBF2
The expression of gene, C are the expression of tomato CBF3 gene.
Fig. 8 is in the embodiment of the present invention 4 under room temperature and cryogenic conditions, and the different MYB screened in wild-type tomatoes are transcribed
The variation of factor expression level, including SlMYB0 (Solyc03g005570), SlMYB10 (Solyc05g055030),
SlMYB15 (Solyc09g090130), SlMYB17 (Solyc05g048830), SlMYB30 (Solyc06g069850),
SlMYB31 (Solyc03g116100), SlMYB46 (Solyc11g065840), SlMYB50 (Solyc06g071690),
SlMYB61 (Solyc01g102340), SlMYB96 (Solyc02g067340), the base of SlMYB106 (Solyc01g010910)
Because of the comparison between expression.
Specific embodiment
The present invention is further explained in the light of specific embodiments, but the present invention is not limited to following embodiments.This
Invent other changes and modification being intended to cover in scope and spirit disclosed by the invention.
Unless otherwise indicated, implementation of the invention will use the obvious botany routine skill of those skilled in the art
Art, tissue cultures, molecular biology, biological physiology are biochemical, DNA is recombinated and bioinformatics technique.These technologies are in the literature
Abundant explanation is carried out.
The building of embodiment 1:SlMYB0 gene overexpression carrier
For the molecular mechanism for understanding plant responding low temperature, SlMYB0 gene has been cloned from tomato dna group.According to coding
Region sequence analysis, designs specific primer SlMYB0-F and SlMYB0-R, and adds restriction enzyme site respectively on primer
(Asc I and Kpn I), sequence is as shown in SEQ ID NO:3 and 4.With PrimerSTAR high fidelity enzyme PCR amplification SlMYB0 piece
Then section carries out digestion to pcr amplified fragment and carrier, SlMYB0 segment is connected on pFGC1008-HA, is overexpressed
Carrier OE.Above-mentioned recombinant plasmid is sent to the sequencing confirmation of Qing Ke company, the nucleotide sequence such as SEQ of resulting gene SlMYB0
Shown in ID No:1;The result shows that the sequence (Solyc03g005570) one announced in the sequence and Solgenomics cloned
It causes.
The amino acid sequence of the protein of gene coding is as shown in SEQ ID No:2.
The building of embodiment 2:SlMYB0 gene mutation carrier
Using CRISPR-P website design SlMYB0 gene target sequence, particular sequence is as shown in SEQ ID No:5
CGAGCTTGAAGAAAGGGTCA.The Bbs I of AtU6-sgRNA-AtUBQ-Cas9 carrier is connected to after the target sequence annealing of synthesis
Then the AtU6-sgRNA-AtUBQ-Cas9 segment newly obtained is connected to the Hind III/ of pCAMBIA1301 carrier by site
Kpn I site.Above-mentioned recombinant plasmid is sent to the sequencing confirmation of Qing Ke company.
Embodiment 3: the building and detection of tomato SlMYB0 transgenic line
The over-express vector pFGC1008::SlMYB0-HA that embodiment 1 obtains and the gene editing that embodiment 2 obtains are carried
Body pCAMBIA1301::AtU6-sgRNA (SlMYB0)-AtUBQ-Cas9 converts Agrobacterium GV3101 respectively, and carries out tomato
Cotyledon infects, and by callus induction, induction of resistance differentiation and culture of rootage obtain tissue-cultured seedling, by T2 for mutant seeds and
It is overexpressed seed and carries out the test of kalamycin resistance and chlorampenicol resistant respectively, select that 3/4 is resistant and remaining 1/4 does not have
The strain of resistance illustrates that the over-express vector that target gene is connected in the strain is inserted into the form of single copy.By these plant
It removes, then carries out single plant sowing.It is overexpressed positive transgenic plant using Western Blot verifying SlMYB0, it is wild as the result is shown
Raw type does not have protein band, and is overexpressed the band (Fig. 1) that strain has SlMYB0-HA, is verified using PCR and sequencing technologies positive
SlMYB0 mutation transgene plant, discovery myb0#13 lack 7 bases, and myb0#14 lacks 14 bases, respectively in original phase
It is mutated at the 7th of adjacent motif (PAM) and the 17th base, and stops translation (Fig. 2) immediately.
The low temperature tolerance ability of embodiment 4:SlMYB0 gene transgenic material detects
The wild-type tomatoes seedling of five leaves wholeheartedly is subjected to 25 DEG C and 4 DEG C processing first, it is as the result is shown (Fig. 3, A and B), low
Temperature can induce the expression (Fig. 3 A) of SlMYB0 gene for 6 hours, while promote within low temperature 12 hours a large amount of accumulation of SlMYB0 albumen
(Fig. 3 B), this illustrates that tomato SlMYB0 responds low temperature stress.
By SlMYB0 gene overexpression strain and mutation obtained in five leaves wild-type tomatoes seedling wholeheartedly and embodiment 3
Body strain carries out 25 DEG C and 4 DEG C processing in artificial incubator, after low-temperature treatment 7 days, by low temperature stress processing group and identical item
The control group for not carrying out low-temperature treatment under part is compared, and observation wild type is overexpressed strain and mutant strain tomato plant
Phenotype (Fig. 4), conductivity (Fig. 5), PSII maximum Photochemical quantum yield (Fv/Fm, Fig. 6) and tomato resist cold gene C BF1
The variation of (Fig. 7 A), CBF2 (Fig. 7 B) and CBF3 (Fig. 7 C) expression.The results show that being overexpressed tomato plant can significantly mention
The lower temperature resistance (Fig. 4) of high tomato, conductivity are substantially less than wild type (WT) and myb0 mutating strain series (Fig. 5).In addition, being overexpressed
Fv/Fm (Fig. 6) the He Kangleng gene (CBF1, CBF2 and CBF3, Fig. 7) of plant is above wild-type tomatoes (WT), and mutant
Strain is minimum.It can be seen that tomato SlMYB0 is just regulating and controlling the low temperature tolerance ability of plant.
In addition, the common knowledge as this field, the nucleotide sequence shown in SEQ ID NO:1 has above-mentioned effect
In the case of, carrying out certain change to it by conventional means will not influence its function, such as be substituted, lack and/
Or increases one or more nucleotide and have and do not change protokaryon nucleotide sequence function, nucleotides sequence with the same function
Column;Or hybridize under strict conditions with sequence shown in SEQ ID NO:1 and nucleotide sequence with the same function, it is described stringent
Condition be in 0.1 × SSPE containing 0.1%SDS or 0.1 × SSC solution containing 0.1%SDS, hybridize at 65 DEG C, and use this
Solution washes film;Or the nucleotide sequence with 90% or more homology and coding identical function protein.
Sequence table
<110>Zhejiang University
<120>tomato SlMYB0 gene and its application in raising plant frigostabile
<160> 5
<170> SIPOSequenceListing 1.0
<210> 1
<211> 756
<212> DNA/RNA
<213> Solanum lycopersicum
<400> 1
atggacagag caccttcttg tgagaaaacg agcttgaaga aagggtcatg ggatcacgaa 60
gaagaccaaa ttctcatctc ttacattaac aaaaatggcc atggcaattg gcgcgcactc 120
cctagacaag ctggattatt gagatgtgga aaaagttgca gattgaggtg gatgaattat 180
ttgagtccac atattaagag gggaaatttc accaaagaag aagaagataa tatcatcaat 240
ttacatgaaa ttcttggaaa tagatggtca gcaatagcag caagattacc gggaagaacg 300
gataatgaaa taaaaaatat ttggcacacc cacttgaaga aaaggctaaa aaattgtcag 360
tctcctcgaa gcttcaaaag acacaaaaaa attaatcaaa taaataattg catgcatgct 420
cctaactcac cagaaatatc gtctagcgag acgtcaatca tgacaaccaa ttcatcatca 480
agtggtactt tcgatacgac gatcgacgat caaatagtga ttaaacaaga agaaatggac 540
tcatcggagt atttcgccaa gatcgatgag agcttctgga cggatgaatt aacgatagag 600
aacaatttcg actttgttac taatatggat ggtgaagaat ttgaaagctt agacatgttt 660
aatagtacaa caataatgga ggatgacatt gacatggact ttttgttcaa ctttttcata 720
aagactgagg aattttcaga attaccagaa ctttga 756
<210> 2
<211> 251
<212> PRT
<213> Solanum lycopersicum
<400> 2
Met Asp Arg Ala Pro Ser Cys Glu Lys Thr Ser Leu Lys Lys Gly Ser
1 5 10 15
Trp Asp His Glu Glu Asp Gln Ile Leu Ile Ser Tyr Ile Asn Lys Asn
20 25 30
Gly His Gly Asn Trp Arg Ala Leu Pro Arg Gln Ala Gly Leu Leu Arg
35 40 45
Cys Gly Lys Ser Cys Arg Leu Arg Trp Met Asn Tyr Leu Ser Pro His
50 55 60
Ile Lys Arg Gly Asn Phe Thr Lys Glu Glu Glu Asp Asn Ile Ile Asn
65 70 75 80
Leu His Glu Ile Leu Gly Asn Arg Trp Ser Ala Ile Ala Ala Arg Leu
85 90 95
Pro Gly Arg Thr Asp Asn Glu Ile Lys Asn Ile Trp His Thr His Leu
100 105 110
Lys Lys Arg Leu Lys Asn Cys Gln Ser Pro Arg Ser Phe Lys Arg His
115 120 125
Lys Lys Ile Asn Gln Ile Asn Asn Cys Met His Ala Pro Asn Ser Pro
130 135 140
Glu Ile Ser Ser Ser Glu Thr Ser Ile Met Thr Thr Asn Ser Ser Ser
145 150 155 160
Ser Gly Thr Phe Asp Thr Thr Ile Asp Asp Gln Ile Val Ile Lys Gln
165 170 175
Glu Glu Met Asp Ser Ser Glu Tyr Phe Ala Lys Ile Asp Glu Ser Phe
180 185 190
Trp Thr Asp Glu Leu Thr Ile Glu Asn Asn Phe Asp Phe Val Thr Asn
195 200 205
Met Asp Gly Glu Glu Phe Glu Ser Leu Asp Met Phe Asn Ser Thr Thr
210 215 220
Ile Met Glu Asp Asp Ile Asp Met Asp Phe Leu Phe Asn Phe Phe Ile
225 230 235 240
Lys Thr Glu Glu Phe Ser Glu Leu Pro Glu Leu
245 250
<210> 3
<211> 30
<212> DNA
<213>artificial sequence (Artificial Sequence)
<400> 3
ttggcgcgcc atggacagag caccttcttg 30
<210> 4
<211> 28
<212> DNA
<213>artificial sequence (Artificial Sequence)
<400> 4
ggggtaccaa gttctggtaa ttctgaaa 28
<210> 5
<211> 20
<212> DNA
<213>artificial sequence (Artificial Sequence)
<400> 5
cgagcttgaa gaaagggtca 20
Claims (7)
1. tomato SlMYB0 gene, which is characterized in that the gene is following 1) -4) in any one nucleotide sequence:
1) nucleotide sequence shown in SEQ ID NO:1;
2) nucleotide sequence shown in SEQ ID NO:1 is substituted, lacks and/or increases one or more nucleotide and has not
Change protokaryon nucleotide sequence function, nucleotide sequence with the same function;
3) hybridize under strict conditions with sequence shown in SEQ ID NO:1 and nucleotide sequence with the same function, it is described tight
Glazing bar part is to hybridize at 65 DEG C, be used in combination in 0.1 × SSPE containing 0.1%SDS or 0.1 × SSC solution containing 0.1%SDS
The solution washes film;
4) there is 90% or more homology with nucleotide sequence 1), 2) or 3) and encodes the nucleotides sequence of identical function protein
Column.
2. by tomato SlMYB0 gene described in claim 1 coding obtain protein, which is characterized in that its with it is following it
One amino acid sequence:
1) amino acid sequence shown in SEQ ID No:2;
2) amino acid sequence shown in SEQ ID No:2 is substituted, lacks and/or increases one or more amino acid and has same
The protein as derived from 1) of isoreactivity.
3. tomato SlMYB0 gene improve plant frigostabile ability in application, which is characterized in that the gene be it is following 1)-
4) any one nucleotide sequence in:
1) nucleotide sequence shown in SEQ ID NO:1;
2) nucleotide sequence shown in SEQ ID NO:1 is substituted, lacks and/or increases one or more nucleotide and has not
Change protokaryon nucleotide sequence function, nucleotide sequence with the same function;
3) hybridize under strict conditions with sequence shown in SEQ ID NO:1 and nucleotide sequence with the same function, it is described tight
Glazing bar part is to hybridize at 65 DEG C, be used in combination in 0.1 × SSPE containing 0.1%SDS or 0.1 × SSC solution containing 0.1%SDS
The solution washes film;
4) there is 90% or more homology with nucleotide sequence 1), 2) or 3) and encodes the nucleotides sequence of identical function protein
Column.
4. application according to claim 3, which is characterized in that make the tomato SlMYB0 by gene overexpression technology
The expression of gene rises.
5. application according to claim 4, which is characterized in that the gene overexpression technology is specific as follows:
Tomato total serum IgE is extracted, reverse transcription obtains cDNA, and using cDNA as template, F and R are primer, expands SlMYB0 gene, will expand
Volume increase object is building up on plant over-express vector;The nucleotide sequence of the primers F and R are as shown in SEQ ID NO:3 and 4;
Plant over-express vector is imported in host cell, it is recycled to infect purpose plant, positive transgenic plant is screened, obtains
Obtain low temperature resistant transgenic plant.
6. application according to claim 5, which is characterized in that over-express vector plasmid is pFGC1008::SlMYB0-HA,
Gene editing vector plasmid pCAMBIA1301::AtU6-sgRNA (SlMYB0)-AtUBQ-Cas9.
7. application according to claim 5, which is characterized in that the host cell is that Bacillus coli cells or Agrobacterium are thin
Born of the same parents.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910094106.5A CN109777811A (en) | 2019-01-30 | 2019-01-30 | Tomato SlMYB0 gene and its application in raising plant frigostabile |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910094106.5A CN109777811A (en) | 2019-01-30 | 2019-01-30 | Tomato SlMYB0 gene and its application in raising plant frigostabile |
Publications (1)
Publication Number | Publication Date |
---|---|
CN109777811A true CN109777811A (en) | 2019-05-21 |
Family
ID=66503747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910094106.5A Pending CN109777811A (en) | 2019-01-30 | 2019-01-30 | Tomato SlMYB0 gene and its application in raising plant frigostabile |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109777811A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110894502A (en) * | 2019-11-13 | 2020-03-20 | 浙江大学 | Tomato SlCYP90B3 gene and application thereof |
CN114369616A (en) * | 2022-01-27 | 2022-04-19 | 上海市农业科学院 | Application of tomato SISPS gene in improving high temperature resistance of plants |
CN117904142A (en) * | 2024-03-18 | 2024-04-19 | 浙江大学海南研究院 | Application of SlMYB gene in improving salt stress resistance of tomatoes |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102796746A (en) * | 2012-08-07 | 2012-11-28 | 山东农业大学 | Gene segment for regulating synthesis of solanaceae flavonoids and caffeoyl quinic acid |
CN107354161A (en) * | 2017-07-31 | 2017-11-17 | 华中农业大学 | Watermelon Cla005622 genes are improving the application in liking warm crop low temperature stress resistance |
-
2019
- 2019-01-30 CN CN201910094106.5A patent/CN109777811A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102796746A (en) * | 2012-08-07 | 2012-11-28 | 山东农业大学 | Gene segment for regulating synthesis of solanaceae flavonoids and caffeoyl quinic acid |
CN107354161A (en) * | 2017-07-31 | 2017-11-17 | 华中农业大学 | Watermelon Cla005622 genes are improving the application in liking warm crop low temperature stress resistance |
Non-Patent Citations (2)
Title |
---|
SOLANUM: "Predicted:solanum lycopersicum transcription factor MYB15 (LOC101262488),mRNA", 《GENBANK登录号:XM_004233992.4》 * |
刘辉,等: "植物应答低温胁迫的转录调控网络研究进展", 《中国农业科学》 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110894502A (en) * | 2019-11-13 | 2020-03-20 | 浙江大学 | Tomato SlCYP90B3 gene and application thereof |
CN114369616A (en) * | 2022-01-27 | 2022-04-19 | 上海市农业科学院 | Application of tomato SISPS gene in improving high temperature resistance of plants |
CN117904142A (en) * | 2024-03-18 | 2024-04-19 | 浙江大学海南研究院 | Application of SlMYB gene in improving salt stress resistance of tomatoes |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109456394A (en) | Tomato SlPIF4 gene, albumen and its application in raising plant frigostabile | |
CN108004224B (en) | Make plant that there is rice ALS mutein and its application of Herbicid resistant | |
CN107164347A (en) | Control Culm of Rice rugosity, tiller number, grain number per spike, mass of 1000 kernel and the ideotype gene NPT1 of yield and its application | |
CN110904071B (en) | Application of RAF49 protein and encoding gene thereof in regulation and control of plant drought resistance | |
CN110669785B (en) | Application of tomato SlLOB40 protein and coding gene thereof in regulation and control of plant drought resistance | |
CN104450744B (en) | A kind of paddy rice SBP box transcription factor genes and its application | |
CN112322644B (en) | Application of tomato SlSPY gene in controlling tomato fruit ripening process | |
CN109777811A (en) | Tomato SlMYB0 gene and its application in raising plant frigostabile | |
CN107299103B (en) | Thick boisiana IpASR gene and its coding albumen and application | |
CN108588092A (en) | A kind of pears anthocyanin synthesis transcription factor PbMYB109 and its application | |
CN101555276A (en) | Cadmium-resistant vegetable protein, coding gene and application thereof | |
CN107523575B (en) | Rice blast resistance gene pi-G3 and application thereof | |
CN108570099A (en) | The application of OsGLP2-1 albumen and its encoding gene in regulating and controlling seed dormancy | |
CN108949786A (en) | Application of the arabidopsis E3 ubiquitinbond enzyme coding gene ATL27 in regulation plant salt resistant character | |
CN111018959A (en) | Application of BMDR protein and coding gene thereof in regulating and controlling plant drought resistance | |
CN113337536B (en) | Application of RS2Z32 gene as plant immune negative regulatory factor in improving crop resistance | |
CN109879947A (en) | 2 gene of moso bamboo transcription factor PheDof and application | |
CN102250923B (en) | cryIAc gene having high lepidopteran pest resistance and application thereof in sugarcane | |
CN108276481A (en) | Upland cotton GhLEA3 genes and its application in terms of low-temperature resistance stress | |
US20170088849A1 (en) | Use of tanac2 protein and encoding gene thereof | |
CN107326035A (en) | A kind of adjusting and controlling rice grain type and the deubiquitination enzyme gene UBP5 of leaf color and its application | |
CN107266542B (en) | Thick boisiana IpLEA gene and its coding albumen and application | |
CN102732553B (en) | Improve the gene engineering method and material of plant products | |
CN113563439B (en) | Fruit shape development related protein, and coding gene and application thereof | |
CN109456983A (en) | Soybean GmERF10 gene and its application |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20190521 |
|
RJ01 | Rejection of invention patent application after publication |