CN112410314A - Acetyl transferase OsG2 gene and application of protein coded by same - Google Patents

Abstract

The invention discloses an acetyl transferase OsG2 gene and application of protein coded by the gene, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively. The invention improves the salt stress resistance of crops such as rice and the like by over-expressing OsG2 gene, provides an important way for cultivating rice with enhanced salt stress resistance, can be applied to agricultural production for cultivating rice with enhanced salt stress resistance, and can save energy and water, utilize saline-alkali soil, increase grain yield and the like.

Description

Acetyl transferase OsG2 gene and application of protein coded by same

Technical Field

The invention relates to an acetyltransferase OsG2 gene and application of a protein coded by the gene, and belongs to the field of genetic engineering.

Background

The life style of the plant for the fixed growth determines that the plant cannot be avoided by moving like an animal when encountering an external adverse environment in the whole life cycle of the growth and development. The external conditions that adversely affect the growth, development and reproduction of plants are collectively referred to as stresses, which are mainly subjected to two major stresses: biological and abiotic stress effects. Biotic stress refers to the damage of plants, animals and microorganisms to plants, such as weeds, insect pests and diseases; the abiotic adversity stress refers to adverse effects on plant growth, development and reproduction caused by excessive or insufficient physical or chemical conditions, and mainly comprises saline-alkali damage, drought, high temperature, low temperature, heavy metal and the like. Under the condition of adversity stress, plants develop a set of self defense systems, form adaptive mechanisms at multiple levels of molecules, physiology, development, morphology and the like, and different adversity stresses can cause specific reactions of the plants in the aspects of gene expression, metabolism, physiological traits and the like.

Salt damage is an abiotic limiting factor which seriously affects the regional distribution and growth and development of plants, is one of the main abiotic adversity stresses which affect the growth and development of plants, can simultaneously cause osmotic stress and ionic toxicity on cells, and causes a series of secondary effects, including causing oxidative stress, destroying cell components such as membrane lipids, proteins and nucleic acids, and causing metabolic disturbance. Osmotic stress refers to that high-concentration salt in soil reduces the water potential of the soil, causes water absorption difficulty of plants, even causes water in plants to seep out, causes water deficiency of the plants and generates physiological drought. In salt stress, ionic poisoning refers to excess Na⁺The concentration inhibits the absorption of other ions by the plant, thereby generating toxic action.

Rice is monocotyledon, is one of the most important grain crops in the world, researches on the molecular biology mechanism of growth and development of the rice in each period and the regulation and control of adversity stress, is helpful to understand the growth and development mechanism of the rice, and has important significance for improving the stress resistance of the rice and ensuring the yield of the rice. Rice belongs to salt sensitive crops, especially in seedling stage and development stage. Under the condition of salt stress, the rice can regulate and control the osmotic regulation mode in the rice body by specifically expressing a large amount of salt-tolerant proteins and a plurality of network signal molecules, so that the stability of the environment in the plant body is maintained, and various influences of the salt stress on the rice are resisted. By researching the response mechanism of rice salt stress, genes related to rice salt resistance are screened, the regulation and control mechanism of the genes is further analyzed, the rice variety with salt stress resistance is cultivated, the planting area of rice is further enlarged, and the purpose of increasing the grain yield is achieved.

Acetylation is one of the covalent modifications of proteins that are ubiquitous in the organism. N-terminal acetylation plays an important role in protein stability and degradation, protein subcellular localization and protein-protein interactions and complex formation, as well as cell growth, metabolism, and disease development. N-terminal acetylation is prevalent in eukaryotes, accounting for approximately 50% -70% of soluble proteins in yeast, approximately 70% -90% in mammals, and is also modified by N-terminal acetylation in archaea and bacteria, only relatively rarely. There are mainly 7N-terminal acetyltransferases that have been discovered so far, but research has been mainly focused on humans, and studies on the function of N-terminal acetyltransferase gene in plants have been relatively rare, especially on the stress resistance of plants.

Disclosure of Invention

The invention aims to solve the technical problem of searching related proteins and coding genes for salt stress resistance of crops to obtain plants with changed stress resistance, so that the crops can be suitable for growing on saline-alkali soil.

The invention provides application of protein encoded by an acetyl transferase OsG2 gene in regulating salt stress resistance of crops, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

The invention further provides an application of protein encoded by the acetyltransferase OsG2 gene in regulating the height of crop plants, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

The invention also provides application of protein encoded by the acetyltransferase OsG2 gene in regulating the size of crop grains, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

As a preferred embodiment of the present invention, the salt stress resistance of crops is improved by overexpressing the acetyltransferase OsG2 gene.

As a preferable embodiment of the invention, the nucleotide sequence of the acetyltransferase OsG2 gene is shown in SEQ ID No: 1 is shown.

As a preferred embodiment of the present invention, the nucleotide sequence is further comprised in SEQ ID No: 1 by adding, substituting, inserting or deleting one or more nucleotides in the nucleotide sequence shown in the formula 1.

In a preferred embodiment of the present invention, the crop plant is a gramineous plant.

In a preferred embodiment of the present invention, the crops include, but are not limited to, gramineae such as rice, corn and wheat.

The acetyltransferase OsG2 gene is one of RICE acetyltransferase family GNAT (GCN5-related N-acetyltransferase, public, expressed) subfamily members, is derived from RICE (Oryza Sativa), has the gene number LOC9269142 in NCBI website (http:// www.ncbi.nlm.nih.gov), and has the gene number LOC _ Os02g46700 in RICE website (http:// RICE. plant biology. msu.edu /); is protein of amino acid sequence shown in SEQ ID NO.2 in a coding sequence table.

For convenience of description, the present invention provides SEQ ID No: 1 is referred to as OsG2 gene. The protein with the amino acid sequence shown in SEQ ID NO.2 is called OsG2 protein.

The invention provides an acetyltransferase OsG2 gene and application of protein coded by the OsG2 gene in salt stress of crops, and provides a candidate gene for researching a salt tolerance regulation mechanism of crops (particularly rice). In the absence of the gene, rice shows increased sensitivity to salt stress and an intolerant phenotype. And the transgenic rice plant with the OsG2 gene over-expressed shows the enhanced salt stress resistance. In addition, further morphological observation of the mutant plant shows that the mutant rice plant is short in height, small in grain size and small in thousand kernel weight, and OsG2 gene can directly or indirectly modify some key genes in rice seed development to further influence the final grain size change.

The expression vector containing the OsG2 gene is introduced into crops, and crop plants with changed stress resistance (salt stress resistance) are screened and obtained.

The OsG2 gene of the invention is continuously expressed in the whole growth cycle of the plant, the OsG2 gene can be detected in different tissues of the plant, and the salt stress treatment finds that the expression level of the OsG2 gene in roots and leaves is increased to a certain extent under the induction of 150mM NaCl.

After the transgenic knockout mutant is treated by 150mM NaCl, the expression level of salt stress related genes (such as OsSOS1/OsSOS2/OsSalT/OsABI5, which are known genes of rice) is remarkably increased to different degrees through detection. Ca when plants are subjected to salt stress²⁺The Salt dependent resistance pathway (Salt excess Sensitive pathway), called SOS pathway for short, is rapidly activated, and OsSOS1 and OsSOS2 are key genes of the SOS pathway. OsSalT is a lectin protein similar to baicalein, and is one of the most significant proteins induced by high salt in rice roots. OsABI5 is a bZIP transcription factor, and is induced to express under the condition of salt stress. The expression level of OsSOS1/OsSOS2/OsSalT/OsABI5 in the mutant is increased, which indicates that OsG2 gene can achieve the aim of salt stress resistance by negatively regulating the expression of the genes.

The invention transfects the plasmid or plant expression vector containing the nucleotide sequence shown in SEQ ID NO.1 into host cells by transgenic technology, wherein the host cells include but are not limited to escherichia coli cells, agrobacterium cells and plant cells; the host cell is then introduced into a crop (e.g., rice).

In conclusion, the research of the invention shows that the protein coded by the acetyltransferase OsG2 gene plays an important role in responding to the saline-alkali stress reaction of crops such as rice and the like and regulating the size of rice grains, and further, the gene can be used for carrying out the genetic improvement on important agronomic traits and stress tolerance of the crops such as rice and the like. The invention improves the salt stress resistance of crops such as rice and the like by over-expressing OsG2 gene, provides an important way for cultivating rice with enhanced salt stress resistance, can be applied to agricultural production to cultivate rice with enhanced salt stress resistance, and has important significance for saving energy and water, utilizing saline-alkali soil, increasing grain yield and the like.

Drawings

FIG. 1 is a schematic diagram of the gene structure of rice acetyltransferase OsG2 gene and the mutation site of a mutant of both alleles of OsG2 gene;

FIG. 2 is an analysis of gene expression of the wild type subsurface and aerial parts OsG2 of Nipponbare under salt stress conditions;

FIG. 3 is a graph of phenotypic analysis of mutant plants treated with 150mM NaCl;

FIG. 4 is the analysis of relative expression of salt stress related genes of rice OsG2 mutant plants;

FIG. 5 is a field phenotype analysis of mutant plants at different growth stages;

FIG. 6 shows the statistics of plant heights of mutant plants in different growth stages of a field;

FIG. 7 is a seed map of wild type Nipponbare and mutants in the hulled condition;

FIG. 8 is a seed map of wild type Nipponbare and mutants with hulls;

FIG. 9 is a diagram showing the phenotype analysis of OsG2 gene overexpression plants treated with 150mM NaCl;

Detailed Description

The following examples are further illustrative of the present invention and are not intended to be limiting thereof.

Example 1 acquisition of transgenic Rice Material

1. Obtaining transgenic mutant plants

Plant materials used in the research comprise wild type Nipponbare paddy rice and two mutant plants, the two mutant plants are named as osg2-1 and osg2-2 respectively, the paddy salt sensitive mutant adopted by the invention is obtained by performing gene editing by using a CRISPR Cas9 technology, the result of the gene editing is that two allelic mutants with different mutation sites are generated, and the editing mode is shown in figure 1.

OsG2 the gene has a total length of 4256bp and has a gene structure as shown in FIG. 1. Wherein NIP represents wild type Nipponbare rice used as control; to construct mutant plants of the OsG2 gene, they were created using CRISPR-Cas9 gene editing technology. The main method comprises the following steps:

the T0 generation transformed rice plant is detected by PCR sequencing, and double-chain homozygous editing mutants are screened out and named as osg2-1 and osg2-2 respectively. Wherein the osg2-1 material editing types are 16-311 th and 548-549 th (taking A in the initiation codon ATG as 1) and two nucleotide sequences are respectively deleted, 298bp nucleotides are deleted, and frameshift mutation is generated, so that the OsG2 gene structure is damaged, and functional OsG2 protein with normal size cannot be expressed; the osg2-2 material editing type 16-647 nucleotide sequence is cut, so that 632bp DNA fragment is lost from the OsG2 gene, the frame shift is caused, and the result is that the OsG2 protein with complete structure cannot be generated, so that the OsG2 protein cannot normally function. Taken together, the above procedure resulted in two different allelic variants of OsG 2: osg2-1 and osg 2-2.

The hygromycin marker gene and the Cas9 gene detection result show that the vectors are separated from the two mutant types. The vector for creating the mutant by the CRISPR Cas9 is pRGEB32(https:// www.addgene.org/63142/), and 3 target sites are designed on the exon of the rice OsG2 gene to knock out OsG2 gene.

The target site sequence is as follows:

target site 1: TGGGGTAGATTTCCGATCTT, respectively;

target site 2: TTGAACGTGGTCAACGGCAA, respectively;

target site 3: TCTCCACTACACCGAGCGTC are provided.

The hygromycin gene identification primer is as follows:

F：CTCCATACAAGCCAACCACG；

R：GGAAGTGCTTGACATTGGGG。

cas9 identifies the primers as:

F：CGATAAGAACCTGCCCAACG；

R：GCTCTTTGATGCCCTCTTCG。

the sequencing primer for CRISPR editing detection is as follows:

F：TACTGCCTCTCTTCCTCGCC；

R：GACACCCCTGCAATTTGAGA。

2. obtaining transgenic over-expressed plants

The other transgenic plant material used in the research is two OsG2 overexpression lines which are uniformly named as OsG2-OE in the invention, and the expression quantity of the OsG2 gene in the two overexpression lines is more than 70 times. The specific procedures for generating overexpression transgenic material are as follows:

firstly, OsG2 specific primers with a Gateway reaction system BP joint are designed, a full-length coding sequence of OsG2 gene is obtained by amplifying cDNA obtained by reverse transcription of total rice RNA by a PCR method, the fragment is constructed on a pDONR223 vector by a BP recombination reaction, and the operation is carried out according to the instruction of a recombination cloning kit provided by Invitrogen company. And then carrying out LR recombination reaction on the BP reaction product and a corresponding expression vector, wherein the expression vector used in the invention is pCAMBI1300-33 and has a strong promoter UBI10, and finally introducing the expression vector containing OsG2 gene coding sequence into a rice variety Nipponbare through an agrobacterium-mediated rice genetic transformation system to finally obtain a transgenic overexpression material with different expression multiples of OsG2 gene.

Primers used to amplify the OsG2 gene coding sequence from the total cDNA were:

F:GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGTTGGACCCAAGATCG

R:GGGGACCACTTTGTACAAGAAAGCTGGGTGTTAGACATGACATCTCGTATCATC

example 2 salt stress treatment analysis of OsG2 response

Salt stress treatment was first performed using wild type nipponica, and the response was analyzed at OsG 2. The specific process is as follows: selecting wild type Nipponbare rice seeds with good development condition, putting the seeds into a culture dish containing a small amount of sterile water under the condition of not shelling, and paving a layer of absorbent paper at the bottom of the culture dish. The culture dish containing the seeds is placed in an incubator at the temperature of 30-35 ℃ for two days, and the seeds are transferred to the incubator at the temperature of about 25 ℃ after exposing white and breaking the breast, so as to achieve the purposes of accelerating germination and promoting root growth. It should be noted that the sterile water in the culture dish needs to be replaced during the seed soaking and germination process to ensure that the seeds can breathe and grow normally.

And selecting rice seedlings with consistent growth conditions after germination, transferring the rice seedlings into a culture box containing Hoagland nutrient solution, selecting the seedlings with consistent growth conditions for salt stress treatment when the seedlings grow in the culture box for about 15 days, and carrying out water culture by using the Hoagland nutrient solution (containing 150mM NaCl) during treatment. Sampling was done before treatment as a control group, and then the above-ground and below-ground parts of the seedlings were sampled separately after 3 days, with sampling repetition of at least three biological repetitions at each time point. And immediately putting the sample into liquid nitrogen for quick freezing after sampling. Then transferred to a-80 ℃ refrigerator for later use.

Extracting total RNA, reverse transcribing to cDNA, and qPCR analyzing OsG2 gene expression with cDNA as template. The results are shown in FIG. 2: with the prolonged salt stress treatment time, the expression level of the OsG2 gene showed a significant rising trend. Therefore, acetyl transferase OsG2 has positive regulatory effects on the salt stress resistance of rice.

The qPCR primers used to identify the OsG2 gene were as follows:

F:GGCCGTTCGCCTTGCT

R:ACCTGGCAACCACCATCTTC

the ACTIN primers used for identification of control were as follows:

F:TGGCATCTCTCAGCACATTCC

R:TGCACAATGGATGGGTCAGA

example 3 transgenic mutant plant salt sensitivity assay

Experimental materials: wild type Nipponbare, OsG2 gene allelic mutant

The treatment method comprises the following steps: the germination pattern of rice seeds was as described in example 2, wild type Nipponbare and mutant seedlings with consistent growth state were selected, transferred to Hoagland nutrient solution containing 150mM NaCl, treated for 0 day, 5 days and 7 days, respectively, and the leaf morphology changes of the control group and the experimental group were observed to record phenotypes. As shown in fig. 3, mutant plants were more susceptible to salt stress relative to wild-type nipponica.

Example 4 analysis of relative expression amounts of salt stress-related genes in Rice OsG2 Gene mutant plants

Experimental materials: wild type Nipponbare, OsG2 gene allelic mutant

The above-ground and underground parts of the plants after 7 days of salt stress treatment in example 3 were sampled separately for not less than 3 biological replicates per sampling; extracting total RNA, carrying out reverse transcription to obtain cDNA, taking the cDNA as a template, and identifying the expression level of each related gene by real-time fluorescent quantitative PCR. The relative expression level of each gene in the sample was calculated with the relative housekeeping gene ACTIN expression level of each gene when the wild type nipponlily was not treated being 1.

Primers used for identifying the OsSOS1 gene were as follows:

F:CGGATCGCTCGAATTTGG

R:GAATGCCGGCTCCGAGTT

primers used for identifying the OsSOS2 gene were as follows:

F:CGCCGTCGCCATGAAG

R:TGGAGCATGCGGTGGTT

primers for identifying the OsABI5 gene were as follows:

F:GAAGAATTCCAGGCTACCACC

R:TTGATCTCAGTCCACACCTCC

primers for identifying the OsSalT gene were as follows:

F:TCCACTGCAAGACTCTGGCC

R:CCAATTGCGTCGATAAGCG

as shown in FIG. 4, the expression level of the salt stress-related gene in the salt-sensitive mutant increased after salt stress compared to that of the wild type Nipponbare before the treatment. After deleting the acetyltransferase OsG2 gene, the expression state of the relevant gene is affected to some extent. Indirectly proves that the acetyl transferase OsG2 protein is involved in the regulation of complex signal pathways related to salt stress.

Example 5 involvement of acetyltransferase OsG2 in regulating plant growth

As shown in FIGS. 5 and 6, corresponding field agronomic trait statistics are carried out on wild type Nipponbare and allelic mutants osg2-1 and osg2-2 of acetyltransferase OsG2 gene at different growth stages, and the statistics result shows that compared with the wild type Nipponbare, the heights of the allelic mutants osg2-1 and osg2-2 of acetyltransferase OsG2 gene are reduced to a certain degree, and the difference is continuously and obviously existed at different growth stages of rice. This suggests that the acetyltransferase OsG2 gene is involved in regulating plant growth.

Example 6 involvement of acetyltransferase OsG2 in regulating seed development

The size of rice grains is closely related to the properties of the rice, such as yield, quality and the like. As shown in fig. 7 and 8, the kernel size of the mutant, including the length and width of the seed, was reduced compared to the wild type, both with and without shelling. The results show that the gene participates in the regulation and control process of rice grain size, and rice seeds are reduced after the gene is deleted, so that the yield of rice is influenced.

Example 7 salt tolerance phenotype analysis of transgenic overexpression lines

In this example, two transgenic overexpression lines with OsG2 gene expression levels increased by more than 70 times were selected and subjected to 150mM NaCl salt stress. The treatment method comprises the following steps: as described in example 2, wild type plants with consistent growth status and overexpression of the gene OsG2 were selected and transferred to Hoagland nutrient solution containing 150mM NaCl for 0 day, 2 days and 5 days, and the leaf morphology changes of the control group and the experimental group were observed for phenotypic recording. As shown in FIG. 9, after 2 days or 5 days of stress, the leaf rolling degree of the OsG2-OE plant is obviously lower than that of the control Nipponbare, so that the OsG2 gene over-expressed transgenic rice line has stronger salt stress tolerance.

Finally, it is also noted that the above-mentioned lists merely illustrate a few specific embodiments of the invention. It is obvious that the invention is not limited to the above embodiments, but that many variations are possible. All modifications which can be derived or suggested by a person skilled in the art from the disclosure of the present invention are to be considered within the scope of the invention.

Sequence listing

<110> Wuhan university

<120> acetyltransferase OsG2 gene and use of protein encoded by the same

<160> 2

<170> SIPOSequenceListing 1.0

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<211> 4256

<212> DNA

<213> Rice (Oryza Sativa)

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agaaccttcc cctgcatctc tctcccgttt ctctccgggt cacgcatcga tcggtctccc 180

ggcgccgtac tgcctctctt cctcgccgcg ctgcaccgag cgctgggtcc gccgattcgg 240

ctgtggcgcg ggtcaaccgc accgacgcgg cgccgcgcct cgacgcccgg aagctgctcc 300

tctccccccg cgcaacgcgc cgcggacctc gtggcggagg ctctggttag tcgtcgtcgt 360

taccggggct tctcatgttg gacccaagat cggaaatcta ccccaccata gcgtatcgtc 420

ctatccagcc ttccgatctc gaggttcttg agaatattca cctcgcgctg tttcccataa 480

ggtgactact gcaaatggat gctccctgat ccctcctttg ctgttcttgc ttatgaatac 540

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ttttttttgg accaattaat cccttaattc ttgtatttgt tttgctcaga tacgagagag 660

agttcttctt gaacgtggtc aacggcaatg gtattatttc ttggggtgct gtggatacca 720

gcagatcaga tgaccgcaga gatgagctga taggctttgt aaccacgaga ataattgcag 780

cacaagatag cgaggtatga catgcaagat tgcatcgatc ttactgatga gctcggtgga 840

actaataatt tggcttgcag attgaggact tgtttaggta taacagctca cgcaaagatc 900

tgacacttct gtatatcctg acgctcggtg tagtggagag ctacagaaac ctcggcatag 960

gttgttacct gctcgtccaa cttagtttta cagtttgtga ttatgatctg attaatcctc 1020

acaagcattc gcgcttgcag catcctcact ggtccgagag gtgattaaat atgctgcaag 1080

tatctcaaat tgcaggggtg tctatttgca tgtcatctca tataaccaac ctgctatcag 1140

cttttacaat aagatgctat ttaagcttgt cagacgactt ccacatttct attacataag 1200

agggcagcat tatgattcat acttgtttgt gtactatgtc aatgggggcc gttcgccttg 1260

ctcaccactg taagtatttc ttgttcttta tctggagaag catgcaagtt ttgtttttag 1320

tagttatccg atgctgtgtt tcaataggat tttactatct gcagttgtca ttcctaactc 1380

tcgttcggat aatatgcaaa ttcgactgcc catgatgaat cgatctcatg aactctgtag 1440

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gttcatactg atctggacat gcccacactg gagaacattt ttcttgtttg actgctttca 1560

gtgaattcag tgtgaaattg aatgcggtcc tttttttaag gaaaacagga gaagaggcct 1620

caacggctta actgttaata tatcaaaaca tataaatgaa tatttacaca aaagctgagg 1680

atacatgagt tctttagaca acataaaact aatagaagct attgaccaaa gagacaaaaa 1740

gttacagctg gacttgccct aacaaccaac catggcagag ttgcatctaa attccttctt 1800

ccaagctggt aatgagagcc ttctatttac aaatacgatt ttattaagag gattacacat 1860

tgtccggcag gataatatat acctaccttg gataatctcc actagttcca actgatataa 1920

ccttttgttg cccatccaac atgtttcttt ttttaaaaaa aaaatccttg aacatgtttc 1980

tttttatcca ttctcttttt actgttttgt ttagtttaca caacttttta aatcgtgtag 2040

aatttgcaac cttaacactc ttaatatcta aataccttac gacatgttaa gccagatggc 2100

gcataaagtg tcatagccca atgtcttagc atgatttctg accatgggat tactgtagca 2160

ccacatacat tattactacc tccgtcccat aataatttta tttctaggat tcaaatttgt 2220

tccaaaatag ttgtcacaat agagtactaa ttgtcccatc aatcacttct tattcaaatt 2280

tcttcctatt ctaccctcaa ccaccctccc gctcttgcat atacaccatt taatgaggga 2340

caccatagtc tttctcctca aaccttaata tatgctaaac aacttagaat tacaattatt 2400

ttgggacaga ggtactacat ttcatgcagt tactttaaca ccacgaggac tactcgactt 2460

tagagataag attatattgg tcaataccat ctctttccgt aatattggag ataagtttct 2520

catgtctctt ttcacaagga tgggaccatg tctcttttaa ccaagcaatg agaaaccaag 2580

tgttcaataa attaagcctc agaatctctc taccgcgtta gggagaagct ctaggtgctg 2640

tcaaactgtc agcttgatga gggttagtgt cgcacccctg gtctaagacc gataacaagg 2700

caacaagcac ataagataac ataaagcctt cttatatcac tatgtgtttt gccaaaatca 2760

cacccaaaca tccagtagtc tgctacatcc aatattctct tcggcttaaa atctgattta 2820

aatatgatat atttttattt caatcctgct caaactggta cttgttggaa gctcgattca 2880

attcagaata atgcttcctg tttaatttgg tccatgctgt ttaaataaga agttcagaac 2940

tcaactacca tattcacata tatgtgcatg tgtgattctg tgctggatgt ggtagaattt 3000

gattaaagta aggaggcagc agacagtgtg ctggtctgca gggagggata gtggtggcta 3060

aagatgattt ccagctgctt tttgttgagg gaggaagggt tggagagata aagggggagg 3120

aaaagtactc actagagaaa atgaagcagg agggttaaaa acgatcctac gtggttttgt 3180

agaaatggtc taaactattt ttgtggtatt ttaccagtcc tgaatgtttg ggggtatttt 3240

ggtaaaaggc caaaagtcat tagtacaatg tgagtcactc gcccgcaacc tttggaccta 3300

tcctgggtta ggtcatcaac tcttggtacc cttatttgtc actaagcatc aaatggatga 3360

cggtgttggt acagggtagc tctaaggcat tactgtgcag acataaggtt ctttaaaggc 3420

acagcaaact tggcctaact tactattaga cataaaacaa gatcattgaa tggctgaggc 3480

aatgtttagg tccttagttt ggtgggcagt aatattttct tgttattgtg tgttgcgact 3540

ttatcaaaga tgtttaaatt taatatcttt tgttgggtgt tgagaggaat tgaacttata 3600

gaccttatga ccaatccaga agaattcaat tgatgtattt ttagttctta ctatggccaa 3660

attatcccag ggttctgata acattatcat gctgccaaaa tgatggtaca ctcgtgctat 3720

caataaataa taacacgtat caatcttgtg cagggaggtc ataacttcat ttgttgttga 3780

cttcagggct ttcctgaaga tggtggttgc caggttctgg aacaaagagg agagaagtac 3840

acccagatgg tccaggtgca aggaatcgac cactctcttg gtatctcaga ataacaagag 3900

gatcattggt ggtgatgata cgagatgtca tgtctaactt taggtgcagc tgggatgttg 3960

ttttctcttg tttttgtgga aacctcagtt tgtttaaaaa ccgtagcttg ctacgttgtt 4020

gtatctgata agttagcaaa ccaggtacat aatttctcga tagtcatagt cacattcatt 4080

tgtaaagaga ggaaaactga aaggagagaa ataaatgtca cctgcttctt gtaacgtttg 4140

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<210> 2

<211> 243

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<213> Rice (Oryza Sativa)

<400> 2

Met Leu Asp Pro Arg Ser Glu Ile Tyr Pro Thr Ile Ala Tyr Arg Pro

1 5 10 15

Ile Gln Pro Ser Asp Leu Glu Val Leu Glu Asn Ile His Leu Ala Leu

20 25 30

Phe Pro Ile Arg Tyr Glu Arg Glu Phe Phe Leu Asn Val Val Asn Gly

35 40 45

Asn Gly Ile Ile Ser Trp Gly Ala Val Asp Thr Ser Arg Ser Asp Asp

50 55 60

Arg Arg Asp Glu Leu Ile Gly Phe Val Thr Thr Arg Ile Ile Ala Ala

65 70 75 80

Gln Asp Ser Glu Ile Glu Asp Leu Phe Arg Tyr Asn Ser Ser Arg Lys

85 90 95

Asp Leu Thr Leu Leu Tyr Ile Leu Thr Leu Gly Val Val Glu Ser Tyr

100 105 110

Arg Asn Leu Gly Ile Ala Ser Ser Leu Val Arg Glu Val Ile Lys Tyr

115 120 125

Ala Ala Ser Ile Ser Asn Cys Arg Gly Val Tyr Leu His Val Ile Ser

130 135 140

Tyr Asn Gln Pro Ala Ile Ser Phe Tyr Asn Lys Met Leu Phe Lys Leu

145 150 155 160

Val Arg Arg Leu Pro His Phe Tyr Tyr Ile Arg Gly Gln His Tyr Asp

165 170 175

Ser Tyr Leu Phe Val Tyr Tyr Val Asn Gly Gly Arg Ser Pro Cys Ser

180 185 190

Pro Leu Ala Phe Leu Lys Met Val Val Ala Arg Phe Trp Asn Lys Glu

195 200 205

Glu Arg Ser Thr Pro Arg Trp Ser Arg Cys Lys Glu Ser Thr Thr Leu

210 215 220

Leu Val Ser Gln Asn Asn Lys Arg Ile Ile Gly Gly Asp Asp Thr Arg

225 230 235 240

Cys His Val

Claims (8)

1. The application of a protein encoded by an acetyltransferase OsG2 gene in regulating the salt stress resistance of crops is disclosed, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

2. The application of a protein encoded by an acetyltransferase OsG2 gene in regulating the height of crop plants, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

3. The application of a protein encoded by an acetyltransferase OsG2 gene in regulating the size of crop grains is disclosed, wherein the amino acid sequence of the protein is shown as SEQ ID No: 2, respectively.

4. The use according to claim 1, wherein the salt stress resistance of the crop plant is improved by overexpression of the acetyltransferase OsG2 gene.

5. Use according to any one of claims 1 to 3, wherein the crop plant is a graminaceous plant.

6. Use according to claim 5, wherein the graminaceous plant is rice, maize or wheat.

7. The use according to any one of claims 1 to 3, wherein the nucleotide sequence of the acetyltransferase OsG2 gene is as set forth in SEQ ID No: 1 is shown.

8. The use according to claim 7, wherein said nucleotide sequence is further comprised in SEQ ID No: 1 by adding, substituting, inserting or deleting one or more nucleotides in the nucleotide sequence shown in the formula 1.

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