CN111411098A

CN111411098A - Rice A L S mutant gene, plant transgenic screening vector pCA L Sm2 containing gene and application thereof

Info

Publication number: CN111411098A
Application number: CN202010379281.1A
Authority: CN
Inventors: 安保光; 陈思兰; 欧阳超; 陈欣妍; 赵惠敏; 龙湍; 吴永忠; 黄培劲
Original assignee: Hainan Bolian Rice Gene Technology Co ltd
Current assignee: Hainan Bolian Rice Gene Technology Co ltd
Priority date: 2020-05-07
Filing date: 2020-05-07
Publication date: 2020-07-14
Anticipated expiration: 2040-05-07
Also published as: CN111411098B

Abstract

The invention relates to the technical field of agricultural biology, in particular to a rice A L S mutant gene, a plant transgenic screening vector pCA L Sm2 containing the gene and application thereof, wherein the amino acid sequence of the rice A L S mutant protein is shown as SEQ ID NO.1, the plant genetic transformation screening vector disclosed by the invention utilizes an expression cassette of the rice A L S mutant gene as a screening marker, herbicides such as pyrimidine salicylic acid and imidazolinone are used as screening agents in a callus screening stage, and the obtained transgenic plant has high resistance of the herbicides such as the pyrimidine salicylic acid and the imidazolinone.

Description

Rice A L S mutant gene, plant transgenic screening vector pCA L Sm2 containing gene and application thereof

Technical Field

The invention relates to the technical field of agricultural biology, in particular to a rice A L S mutant gene, a plant transgenic screening expression cassette containing the gene, a plant transgenic screening vector containing the expression cassette and application thereof.

Background

With the rapid development of genetic engineering and molecular biology techniques, the application range of transgenic technology is more and more extensive. The transgenic technology has a plurality of advantages, such as widening available gene resources and creating new germplasm resources; can carry out directional and fixed-point variation and selection on plant physical traits; provides a new way for cultivating high-yield, high-quality and high-resistance fine varieties and the like. Transgenic crops are approved to be commercially planted in 1996, and 23 transgenic crops are totally approved for commercial production in 2017 worldwide, and the transgenic crops relate to more than 16 types of target traits including insect resistance, herbicide resistance, disease resistance, fertility change, quality improvement and the like. According to statistics, transgenic crops such as soybeans, corns, cottons, rapes and the like mainly resisting herbicides and insects are planted in 26 countries and regions in the world in 2017, and the area reaches 1.9 hundred million hectares. The large-area popularization of the transgenic crops makes great contribution to the global agricultural production.

At present, with the continuous popularization of transgenic products, people tend to be objective and positive in attitude of the transgenic products, but the controversial effects on the transgenic products are still serious, and the potential safety risk problems of the transgenic products are still generally concerned, so that the transgenic products need to be strictly controlled and supervised. One of the key issues for transgenic crops is the potential risk that a selectable marker may pose, and its resistance to target organisms, allergenicity of the expressed protein, and its effects on the nutrients, natural toxins and anti-nutrient content of the recipient crop itself are unknown after transfer into the plant. The most used at present are antibiotic and herbicide screening markers, such as hygromycin-HPT screening system, kanamycin-NPTII screening system, glufosinate-Bar screening system, etc. Most of these selection markers are foreign genes derived from bacteria, etc., which is also one of the causes of public concern. The risks and concerns posed by foreign genes can be eliminated if plants can be re-transformed with genes endogenous to the plant as selectable markers.

Acetolactate synthase (acetolactate synthase, A L S; EC2.2.1.6) is a key enzyme catalyzing the initiation of the synthesis of branched-chain amino acids (isoleucine, leucine and valine) in plants (Herrera-Estra L D, M essens E, et al, chiral genes AS major selectable markers in plants, 1983,2(6): 987-19-995.), is absent in animals, so that the biosynthesis of branched-chain amino acids can be blocked by inhibition of the A L S enzyme for the purpose of eliminating plant weeds, and is harmless to humans and animals.A mutation at a certain site in the amino acid sequence of A L S has been developed and applied against this enzyme, for example sulfonylureas, imidazolinones, pyrimidinamides and sulfonamides, etc., makes the A L S protein structure altered, resulting in binding of inhibitors of A L S, A6723S, A L, which makes it impossible to produce resistance to microorganisms (hormone, S23, scientific, S23, 11. 12. this patent publication No. 7-S. 11. the invention also discloses that the enzyme can reduce the sensitivity of microorganisms to plants (hormone, S23, Escherichia coli, S23, Escherichia coli, S23, Escherichia coli, III) and S23. 9. A3. supplement, III. 7. 9. A3. A.

Disclosure of Invention

The invention aims to provide a rice A L S mutant protein and a coding gene thereof, and provides a vector for applying a plant genetic transformation screening by using a plant endogenous gene as a screening marker to solve the problem of potential safety risk caused by using an exogenous screening marker in the current genetic transformation.

In order to achieve the purpose, the technical scheme of the invention is as follows:

according to the first aspect, the invention provides rice A L S mutant protein, wherein the A L S mutant protein has amino acid mutations at positions 95, 548 and 627 compared with wild type A L S protein.

In the A L S mutant protein, the amino acid mutations at positions 95, 548 and 627 can be the mutation of the amino acids at positions 95, 548 and 627 of the wild-type A L S protein of the plant into any one of alanine, serine, phenylalanine, tyrosine, valine, cysteine, glycine, histidine, arginine, lysine, isoleucine, leucine, tryptophan, methionine, asparagine, glutamine, aspartic acid, glutamic acid and threonine.

Preferably, the a L S mutein is mutated from Gly to Ala at position 95, Trp to L eu at position 548 and Ser to Ile at position 627 relative to the wild-type a L S protein.

More preferably, the a L S mutein has the amino acid sequence of (1) or (2) below:

(1) an amino acid sequence shown as SEQ ID NO. 1;

(2) the amino acid sequence of the A L S mutant protein which is obtained by substituting, inserting or deleting one or more amino acids in the amino acid sequence shown as SEQ ID NO.1 and can enable plants to have the resistance of A L S inhibitor herbicides.

The rice A L S mutant protein provided by the invention has higher resistance to imidazolinone, pyrimidine salicylic acid, sulfonylurea or sulfonamide herbicides.

The invention provides a nucleic acid for coding the A L S mutant protein, and all nucleic acid sequences capable of coding the A L S mutant protein are in the protection scope of the invention, such as a nucleotide sequence shown as SEQ ID NO. 2.

The present invention provides biological material comprising a nucleic acid encoding the a L S mutein, in particular an expression cassette, a vector, a host cell or a transgenic plant cell line comprising a nucleic acid encoding the a L S mutein.

The invention provides any one of the following applications of the A L S mutant protein or the nucleic acid encoding the A L S mutant protein or the biological material containing the nucleic acid:

(1) use in conferring resistance to an a L S inhibitor herbicide or increasing resistance to an a L S inhibitor herbicide in a plant;

(2) the application in preparing transgenic plants;

(3) the application in the improvement of plant germplasm resources;

(4) the application of the gene expression vector in the selection of plant genetic transformation or the construction of plant genetic transformation selection vectors.

The A L S inhibitor herbicide provided by the invention comprises, but is not limited to, imidazolinone, pyrimidine salicylic acid, sulfonylurea or sulfonamide herbicides.

Plants of the invention include, but are not limited to, rice, maize, wheat, soybean, sorghum, peanut, sesame, cotton, linseed, grain, oat, rapeseed, barley, rye, millet, tobacco, highland barley, arabidopsis, and the like. Preferably, the plant is rice, maize, wheat, soybean, sorghum, peanut or millet.

In a second aspect, the present invention provides a plant transgene screening expression cassette having a plant endogenous gene as a screening marker, the plant endogenous gene being an a L S mutant gene.

Preferably, the A L S mutant gene is a rice A L S mutant gene.

More preferably, the protein encoded by the rice A L S mutant gene (A L Sm2) is the A L S mutant protein disclosed by the invention.

The invention finds that the A L S mutant protein with the sequence shown in SEQ ID NO.1 is more suitable to be used as a screening marker, and can more efficiently play the function of the screening marker in the process of plant gene transformation.

The nucleotide sequence of the rice A L S mutant gene (A L Sm2) can be the nucleotide sequence shown in SEQ ID NO. 2.

The plant transgene screening expression cassette further comprises a promoter and a terminator for initiating and terminating transcription of the a L S mutant gene.

The promoter may be a plant constitutive promoter or a plant tissue specific promoter.

The plant constitutive promoter can be a rice A L S gene promoter, a Ubi promoter or an Actin promoter of rice or corn, and the plant tissue specific promoter can be a Rubisco small subunit promoter or a Cab promoter.

Preferably, the promoter is a rice A L S gene promoter.

The terminator may be a DNA sequence capable of terminating gene transcription in plants, including a rice A L S gene terminator, a Ubi terminator, and the like.

Preferably, the terminator is a rice Ubi terminator.

The invention discovers that the transcription of the rice A L S mutant gene can be better controlled by adopting the rice A L S gene promoter and the Ubi terminator to cooperate and regulate, so that the high-efficiency, stable and appropriate expression of the A L S mutant gene can be better controlled, and the A L S gene mutant can better exert the function of screening and marking.

As a preferred scheme of the invention, the nucleotide sequence of the plant transgenic screening expression cassette is shown as SEQ ID No. 3.

The invention provides application of the A L S mutant gene as a screening marker for plant genetic transformation.

Based on the plant transgenic screening expression cassette, the invention further provides a plant genetic transformation screening vector, which contains the plant transgenic screening expression cassette.

Preferably, the plant genetic transformation screening vector is a plant binary expression vector, and can be used for genetic transformation by cloning other expression cassettes into the vector; the other expression cassettes refer to expression cassettes other than the plant transgene screening expression cassette, and include but are not limited to fluorescent protein expression cassettes, GUS reporter gene expression cassettes, insect-resistant expression cassettes, herbicide-resistant expression cassettes and the like.

More preferably, the plant genetic transformation screening vector of the present invention further comprises a series of multiple cloning sites such as AfeI, AvrII, PmlI, SnaBI, AloI, PmeI, etc. to allow for the subsequent cloning of the gene of interest.

As a preferred scheme of the invention, the plant genetic transformation screening vector provided by the invention is pCA L Sm2, and the nucleotide sequence of the vector is shown as SEQ ID NO. 4.

The plant genetic transformation screening vector can be prepared by the following method:

(1) constructing a plant transgenic screening expression cassette, namely placing an A L S mutant gene with a sequence shown as SEQ ID NO.2 under the drive of a promoter A L Spro of the gene to express, and terminating expression by a rice Ubi terminator at the downstream of the mutant gene to obtain the plant transgenic screening expression cassette with the sequence shown as SEQ ID NO. 3;

(2) the plant transgenic screening expression cassette is connected with a plant binary expression vector pC0310 to obtain the plant genetic transformation screening vector.

The invention also provides application of the A L S mutant protein or the plant transgenic screening expression cassette in serving as a plant genetic transformation screening marker.

The invention also provides application of the A L S mutant protein or the plant transgenic screening expression cassette or the plant genetic transformation screening vector in plant genetic transformation.

The application specifically comprises the following steps: after the plant transgenic screening expression cassette or the plant genetic transformation screening carrier is transferred into the plant callus, the callus is inoculated into a screening culture medium added with herbicide in the screening stage for resistance screening.

The herbicide may be a pyrimidinylsalicylate or imidazolinone herbicide, for example: bispyribac-sodium, imazapyr or imazethapyr.

Preferably, the screening culture medium contains 0.25-1 mu mol/L Bispyribac-sodium, 200-1000 mu g/L Mexican-P or 300-1000 mu g/L imazethapyr.

In the screening medium, the screening efficiency is preferably good when the screening medium contains 0.3-0.4 mu mol/L bispyribac-sodium, more preferably 0.4 mu mol/L bispyribac-sodium, or the screening efficiency is good when the screening medium contains 200-20 mu g/L imazapyr, more preferably 250-300 mu g/L imazapyr, or the screening efficiency is good when the screening medium contains 300-500 mu g/L imazethapyr, more preferably 400-500 mu g/L imazethapyr.

Further, the application specifically comprises: and in the differentiation stage after the plant transgenic screening expression cassette or the plant genetic transformation screening vector is transferred into the plant callus, performing differentiation culture on the positive callus obtained from the screening culture medium by adopting a differentiation culture medium containing herbicide.

Preferably, the differentiation medium contains 0.05-1 mu mol/L Bispyribac-sodium, 25-1000 mu g/L Mexican-P or 25-1000 mu g/L imazethapyr.

The differentiation medium preferably contains 0.05-0.25 mu mol/L bispyribac-sodium, more preferably contains 0.1 mu mol/L bispyribac-sodium to obtain good differentiation efficiency, or preferably contains 30-100 mu g/L imazapyr, more preferably contains 50 mu g/L imazapyr to obtain good differentiation efficiency, or preferably contains 30-100 mu g/L imazethapyr, more preferably contains 50 mu g/L imazethapyr to obtain good differentiation efficiency, and simultaneously effectively inhibits the non-transgenic callus from differentiating into seedlings.

Further, the application specifically comprises: and in the rooting stage after the plant transgenic screening expression box or the plant genetic transformation screening vector is transferred into the plant callus, carrying out rooting culture on the positive seedling obtained by differentiation culture by adopting a rooting culture medium containing herbicide.

Preferably, the rooting medium contains 0.05-10 mu mol/L Bispyribac-sodium, 25-1000 mu g/L Mexican-P or 25-1000 mu g/L imazethapyr.

The rooting medium preferably contains 0.05-5 mu mol/L bispyribac-sodium, more preferably contains 0.1 mu mol/L bispyribac-sodium to obtain good rooting efficiency, or preferably contains 50-100 mu g/L imazapyr, more preferably contains 50 mu g/L imazapyr to obtain good rooting efficiency, or preferably contains 50-100 mu g/L imazethapyr, more preferably contains 50 mu g/L imazethapyr to obtain good rooting efficiency, and simultaneously effectively inhibits the rooting of the non-transgenic differentiated seedlings.

Taking rice as an example, other plant transgenic methods can refer to rice:

1) induction: after rice seeds are shelled and disinfected, mature embryos are inoculated in an induction culture medium to induce embryonic callus, and dark culture is carried out for 30-50 days at the temperature of 27 ℃;

2) infection: separating the callus obtained in the step 1) from endosperm and buds, inoculating the callus into a suspension of agrobacterium carrying the plant genetic transformation screening vector (suspending the agrobacterium carrying the plant genetic transformation screening vector in a suspension culture medium) for infection, standing for 30 minutes at room temperature, and then airing for later use;

3) co-culturing: transferring the dried callus into a co-culture medium, and performing dark culture at 22 ℃ for 3 days until thalli appear on the surface of the callus;

4) screening: cleaning the co-cultured callus, inoculating to a screening culture medium containing bispyribac-sodium, imazapyr or imazethapyr, performing dark culture at 27 deg.C for 30-50 days, and screening for resistance;

5) differentiation: inoculating the obtained resistant callus onto a differentiation culture medium added with bispyribac-sodium, imazapyr or imazethapyr, and performing illumination culture at 27 ℃ for 25-40 days until seedlings are differentiated;

6) rooting: inoculating the seedling to a rooting culture medium added with bispyribac-sodium, imazapyr or imazethapyr for rooting, performing illumination culture at 30 ℃ for 10-20 days, performing PCR detection, and selecting the plant which is detected to be positive for planting;

the specific formula of the culture medium is as follows:

the induction medium is N6D medium, which is a medium taking N6 medium as a basic medium, and contains 3 mg/L of 2, 4-dichlorophenoxyacetic acid (2,4-D), 0.3-0.6 g/L of hydrolyzed Casein (CH), 0.3-0.5 g/L of proline (Pro), 30 g/L of sucrose, 3 g/L of plant gel (Phytagel) and 5.9 of pH value;

the suspension culture medium is N6-AA culture medium, which takes N6 culture medium AS basic culture medium, and contains 2, 4-dichlorophenoxyacetic acid (2,4-D) with the concentration of 2 mg/L, hydrolyzed Casein (CH) with the concentration of 0.3-0.6 g/L, proline (Pro) with the concentration of 0.3-0.5 g/L, sucrose with the concentration of 20 g/L, glucose with the concentration of 10 g/L, Acetosyringone (AS) with the concentration of 100-;

the co-culture medium is N6-AS culture medium, which takes N6 culture medium AS basic culture medium, and contains 2, 4-dichlorophenoxyacetic acid (2,4-D) with the concentration of 2 mg/L, hydrolyzed Casein (CH) with the concentration of 0.3-0.6 g/L, proline (Pro) with the concentration of 0.3-0.5 g/L, sucrose with the concentration of 20 g/L, glucose with the concentration of 10 g/L, Acetosyringone (AS) with the concentration of 100-;

the screening culture medium is N6S culture medium, which is culture medium taking N6 culture medium as basic culture medium, and contains 2, 4-dichlorophenoxyacetic acid (2,4-D) with concentration of 2-3 mg/L, hydrolyzed Casein (CH) with concentration of 0.6-1 g/L, proline (Pro) with concentration of 0.5-1.5 g/L, sucrose with concentration of 30 g/L, plant gel (Phytagel) with concentration of 3 g/L, and cephalosporin (Cn) with concentration of 500 mg/L, bispyribac sodium with concentration of 0.25-1 μmol/L, or imazapyr with concentration of 200 μ g/L, or imazethapyr with concentration of 300 μ g/L, and pH value of 5.8;

the differentiation medium is MSRe medium, which takes MS medium as basic medium, and contains 1-2 mg/L concentration of Kinetin (KT), 0.5-2 mg/L concentration of α -naphthylacetic acid (NAA), 20-40 g/L concentration of sorbitol, 30 g/L concentration of sucrose and 3 g/L concentration of plant gel (Phytagel), wherein the concentration of bispyribac-sodium serving as screening agent in the differentiation medium is 0.05-1 mu mol/L, or the concentration of imazapyr is 25-1000 mu g/L, or the concentration of imazethapyr is 25-1000 mu g/L, and the pH value is 5.9;

the rooting culture medium is 1/2MSR culture medium, which is culture medium using 1/2MS culture medium as basic culture medium, containing 20 g/L of sucrose, 0.5-1 mg/L of paclobutrazol and 3 g/L of plant gel (Phytagel), wherein the concentration of bispyribac-sodium as screening agent in the rooting culture medium is 0.05-10 mu mol/L, the concentration of imazapyr is 25-1000 mu g/L or the concentration of imazethapyr is 25-1000 mu g/L, and the pH value is 5.8;

the invention has the beneficial effects that the invention provides rice A L S mutant protein which can lead the plant to be highly resistant to A L S inhibitor herbicides, and also provides a plant transgenic screening expression box using the rice A L S mutant gene as a screening marker, a plant genetic transformation screening carrier and a corresponding gene transformation screening method.

Drawings

FIG. 1 is an electrophoretogram of pCA L Sm2 vector digested by XhoI in example 1 of the present invention, wherein M is Marker, CK is an undigested pCA L Sm2 recombinant plasmid, and 1-8 are digested pCA L Sm2 recombinant plasmid, which can cut out a fragment of about 1.7kb in size.

FIG. 2 shows the results of PCR detection of Agrobacterium after transformation in example 2, wherein M is Marker, 1 is negative control (water as template), 2 is pCA L Sm2 recombinant plasmid positive control, and 3-11 is pCA L Sm2 recombinant plasmid Agrobacterium monoclonal antibody sample (5 is negative).

FIG. 3 is a map of the pC0310 vector in example 1 of the present invention.

FIG. 4 is a map of pCA L Sm2 vector in example 1 of the present invention.

FIG. 5 is a comparison chart of critical concentration test of bispyribac-sodium in seedling stage of common rice in example 3, wherein the left side of the seedling pot is 9311, the right side is ZH11, wherein 0 represents no bispyribac-sodium, 10 × represents 300 mg/L, and 20 × represents 600 mg/L.

FIG. 6 is a test chart of critical concentration of imazapyr in seedling stage of ordinary rice in example 3, wherein 0.2 × represents 19.6 mg/L, 0.5 ×,1 ×,2 × and 5 × are corresponding multiples respectively, and seedlings in seedling pots are ZH 11.

FIG. 7 shows critical concentration tests of imazethapyr in seedling stage of ordinary rice in example 3 of the present invention, wherein 5 × represents 375 mg/L, 20 ×, 50 ×, 100 × and 300 × are corresponding multiples respectively, and seedlings in seedling pots are ZH 11.

FIG. 8 shows the results of critical concentration test of rice calli on bispyribac-sodium resistance in example 4 of the present invention, wherein N6 is the result of screening calli on culture without screening pressure for 40 days, and N6+ is the screening pressure of bispyribac-sodium added for 0.25, 0.5, 1 and 2. mu. mol/L, respectively.

FIG. 9 shows the results of callus screening with bispyribac-sodium screening medium in example 8 of the present invention for 40 days.

FIG. 10 shows the results of differentiation of callus 30d by adding bispyribac-sodium, imazapyr or imazethapyr to the differentiation medium in examples 14, 20 and 28 of the present invention, wherein 1 and 2 are differentiation cultures with bispyribac (0.1. mu. mol/L), 3 and 4 are differentiation cultures with imazapyr (50. mu.g/L), and 5 and 6 are differentiation cultures with imazethapyr (50. mu.g/L), wherein 1, 3 and 5 are non-transgenic calli and 2,4 and 6 are transgenic positive calli.

FIG. 11 shows the results of rooting 15 days after adding bispyribac-sodium, imazapyr or imazethapyr to the rooting medium in examples 37, 47 and 55 of the present invention, wherein 1 and 2 are rooting culture with bispyribac (0.1. mu. mol/L), 3 and 4 are rooting culture with imazapyr (50. mu.g/L), and 5 and 6 are rooting culture with imazethapyr (50. mu.g/L), wherein 1, 3 and 5 are rooting for non-transgenic differentiated seedlings, and 2,4 and 6 are rooting for transgenic positive differentiated seedlings.

FIG. 12 is a PCR detection electrophoretogram of transgenic sample plants in example 63 of the present invention; wherein M is Marker, 1 is H₂O and 2 are genome DNA of a ZH11 non-transgenic plant, 3 is a plasmid positive control, and 4-24 are genome DNA of a transgenic plant obtained by screening.

FIG. 13 shows the results of the herbicide resistance test of T0 transgenic line in example 64 of the present invention; wherein, a-d: spraying 90mg/m after the bispyribac-sodium screening plant line is transplanted²And a-d are respectively before spraying, 7 days, 14 days and 21 days after spraying, arrows in the figure show that wild type contrast ZH11 completely dies after 14 days of spraying, e and f are respectively to spray 2 × (196 mg/L) imazapyr after the imazapyr screening strain is transplanted, e is to spray 20 × (1500 mg/L) imazethapyr after 21 days of spraying, g-h is to spray imazethapyr screening strain, g is to spray 25 (1500 mg/L) imazethapyr before and h is to spray 21 days, wherein ZH11 is wild type contrast, and 25, 25-1, 38-1, 41-1 and 50-1 are all transgenic strains.

Detailed Description

Preferred embodiments of the present invention will be described in detail with reference to the following examples. It is to be understood that the following examples are given for illustrative purposes only and are not intended to limit the scope of the present invention. Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the spirit and scope of this invention.

The experimental procedures used in the following examples are all conventional procedures unless otherwise specified.

Materials, reagents and the like used in the following examples are commercially available unless otherwise specified.

Example 1 construction of a vector for genetic transformation screening of plants containing the Rice A L S mutein

1. Obtaining of Rice A L S mutant protein

The invention carries out a large amount of analysis and combination comparison on the existing herbicide resistance mutant sites of a plant A L S, and obtains an A L S mutant protein (the amino acid sequence is shown as SEQ ID NO.1, and the nucleotide sequence of the coding gene is shown as SEQ ID NO. 2) with amino acid mutation at the 95 th position (Gly is mutated into Ala), the 548 th position (Trp is mutated into L eu) and the 627 th position (Ser is mutated into Ile) relative to the rice wild type A L S protein from different site combinations, wherein the mutant protein has higher A L S inhibitor resistance compared with each single-point mutant at the 95 th position, the 548 th position and the 627 th position and other site combination mutants, solves the problem that each mutant has single-point resistance to herbicides, has higher resistance to imidazolinones, pyrimidine salicylic acids, sulfonylureas or sulfonamide herbicides, can endow the plant with high resistance to a plurality of A L S inhibitor herbicides, and can provide an effective solution for the rotation of a plurality of herbicides.

2. Preparation of plant transgene screening expression cassette

The construction method of the plant transgenic screening expression cassette OsA L SP-A L Sm2-OsUbiT (the sequence is shown as SEQ ID NO. 3) of the invention is as follows:

designing primers 0310-AA2U-F/0310-AA2U-Rv1 to amplify a promoter OsA L SP fragment from a rice genome, amplifying a target gene A L Sm2 fragment from a synthetic rice A L S mutant gene (A L Sm2) fragment by using primers 0310-AA2U-F2/0310-AA2U-Rv2, amplifying a terminator OsUbiT fragment from the rice genome by using primers 0310-AA2 469-F6862/0310-AA 2U-Rv, wherein about 15 nucleotide sequences are repeated at the corresponding connecting positions of the 5 'ends of the primers 0310-AA2U-F and 0310-AA2U-Rv, 15bp repeats are also arranged at the 5' ends of the upper and lower primers of adjacent fragments (0310-AA2U-Rv1, 0310-AA2 AA U-F2, 0310-AA2 Rv 03172) and recombining the gene AsUbiT fragment with Asubb 2 and then using primers 0310-AA 2-03172 to obtain a recombinant gene Asubb 2.

The primer sequences are as follows:

0310-AA2U-F:CGTTTTTAATGTATGCTCCACCATGttggCGTAAAGTCTTCACTCCTCCCCC(SEQID NO.5)；

0310-AA2U-Rv1：CGTAGCCATGGTGGGTGGTGGCGG(SEQ ID NO.6)；

0310-AA2U-F2：CACCCACCATGGCTACGACCGCCGC(SEQ ID NO.7)；

0310-AA2U-Rv2：GGCTGAGGACTCTAGATTAATACACAGTCCTGCCATCA(SEQ ID NO.8)；

0310-AA2U-F3：TGTATTAATCTAGAGTCCTCAGCCATAGAGCTG(SEQ ID NO.9)；

0310-AA2U-Rv:TGCCCGGGCCTGCAgGACAAATTTGTTTGTCAGATCAAATTTTTAAGC(SEQ IDNO.10)。

the PCR amplification reaction system is as follows:

the PCR amplification procedure was as follows: pre-denaturation at 94 ℃ for 3 min; denaturation at 94 ℃ for 30s, annealing at 55-65 ℃ for 30s, extension at 68 ℃ for 3min, and 35 cycles; extension was carried out at 68 ℃ for 10min and at 16 ℃ was stopped.

PCR products amplified by primers 0310-AA2U-F and 0310-AA2U-Rv1 are OsA L SP fragments, the size of the products is 2180bp which is recovered by 1% agarose gel electrophoresis, PCR products amplified by primers 0310-AA2U-F2 and 0310-AA2U-Rv2 are A L Sm2 fragments, the size of the products amplified by 1% agarose gel electrophoresis is 1941bp, PCR products amplified by primers 0310-AA2U-F3 and 0310-AA2U-Rv are OsUbiT fragments, and the size of the products amplified by 1% agarose gel electrophoresis is 310 bp.

3. Construction of plant genetic transformation screening vector

The amplification product in 1 is inserted into a pC0310 vector (pC0310 is a pC AMBIA1300 vector skeleton supported by the inventor and is obtained by modification, wherein the pC0310 mainly deletes a hygromycin screening element and an unnecessary region of an adjacent region so that the interior of the T-Border does not contain other bacterial sequences except a multiple cloning site, therefore, a plant-derived sequence is subsequently connected into the T-Border, the public transgenic concern is reduced when the T-Border is transferred into a plant, and a vector map is shown in figure 3) between BstXI and PstI double enzyme cutting sites, wherein the method comprises the following steps:

(1) vector plasmid pC0310 was double digested with BstXI + PstI, electrophoresed through an agarose gel using E.Z.N.A.

The Extraction kit (Omega, the same below) recovered a band of about 7kb in size, giving a pC0310 linear fragment.

The BstXI + PstI double-enzyme digestion reaction system is as follows:

(2)2 ×L lightening Cloning Kit connection Kit

OsA L SP-A L Sm2-OsUbiT expression cassette is connected to pC0310 vector, and the connection system is as follows:

and (3) connecting procedures: 50 ℃ for 30 min.

(3) And (2) transforming, namely adding 2 mu l of the ligation product into an escherichia coli competent cell, slightly mixing the ligation product uniformly, carrying out ice bath for half an hour, transforming the escherichia coli competent cell by using an electrotransfer instrument with 1.8KV electric shock, adding 1ml of L B culture medium, carrying out shaking culture at 37 ℃ and 220rpm for 1h, centrifuging at 5000rpm for 30s, discarding 800 mu l of supernatant, uniformly mixing the residual thallus with the culture medium, coating the mixture on a L B plate containing kanamycin, carrying out culture at 37 ℃ for about 16h, picking out single colonies, carrying out colony PCR (polymerase chain reaction) verification by using specific primers (0310-F2 and 0310-R2), picking out positive colonies, shaking the colonies overnight at 37 ℃ and 220rpm, extracting plasmids by using a high-purity plasmid miniextraction kit (Zhongkeitai), carrying out enzyme digestion detection correct (as shown in figure 1), carrying out sequencing and sending a sequence to be named pCA L Sm2, wherein a vector map is shown in figure 4, and the nucleotide sequence.

The primer sequence is as follows:

0310-F2:GGGCCATACTTGTTGGATATCAT(SEQ ID NO.11)；

0310-R2:TTGTTCATGGCGTAATGTCTCC(SEQ ID NO.12)。

example 2 Agrobacterium transformation and identification

Agrobacterium EHA105 competent cells preserved at-80 ℃ were added with 1. mu.l of the correctly sequenced pCA L Sm2 plasmid obtained in example 1, transformed by 1.8KV electric shock, spread on YEP plates containing kanamycin, rifampicin and streptomycin, cultured at 28 ℃ for about 48h, single colonies were picked up and shaken overnight, PCR verification of bacterial solutions was performed with specific primers (0310-F2 and 0310-R2) (see FIG. 2), fragments of about 900bp were obtained by amplification, positive clones (engineering Agrobacterium) were selected, shaken for 36-48h, and the bacterial solutions were preserved for infection.

Example 3 Critical concentration test of Bispyribac-sodium, imazapyr and imazethapyr in the seedling stage of ordinary rice

Bispyribac-sodium is a herbicide for rice fields, common rice has resistance to the bispyribac-sodium, so that the herbicide with a medicament specified concentration sprayed on the rice cannot cause damage to the rice, the safety concentration of most spraying is 30 mg/L, imazapyr is a nonselective sterilant herbicide, the common rice has no resistance to the common rice, the spraying concentration is recommended to be 95-98 mg/L, imazethapyr is an imidazolinone herbicide, is mainly used for preventing and killing gramineous weeds and broadleaf weeds in leguminous crops, has the advantages of strong selectivity, wide weed control spectrum, high activity and the like, the recommended concentration is 75 mg/L, and the common rice has weak resistance to the common rice.

This example analyzes the critical concentrations of rice resistance to Bispyribac-sodium, imazapyr and imazethapyr, and the results of experimental tests are shown in FIGS. 5,6 and 7. for Bispyribac-sodium, whether it is japonica rice mid-flower 11(ZH11) or

indica rice

9311, 20 × (60 mg/m) is sprayed during the seedling stage²) Withering and dying above the concentration, selecting 90mg/m for testing the transgenic line with higher resistance²As the spraying concentration, the japonica rice middle flower 11(ZH11) is sprayed with the concentration of 0.5 × (49 mg/L) to wither and die in the seedling stage for the imazapyr, 2 × (196 mg/L) is selected as the spraying concentration for testing the transgenic line with higher resistance, and 20 × (1500 mg/L) is selected as the spraying concentration for the imazethapyr, the japonica rice middle flower 11(ZH11) is sprayed with the concentration of 5 × (375 mg/L) to wither and die in the seedling stage for testing the transgenic line with higher resistance.

Example 4 screening pressure test of callus period ZH11 Bispyribac-sodium

This example investigated the critical concentration of ZH11 for bispyribac-sodium resistance during callus period and the results are shown in FIG. 8. for bispyribac-sodium, callus proliferation was inhibited by adding 0.25. mu. mol/L or more to N6 medium.

EXAMPLE 5 Bispyribac-pCA L Sm2 genetic transformation System-Screen (1)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of the rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after the callus is co-cultured for 3 days, the callus is washed for 5-6 times, transferred to a resistance screening culture medium containing bispyribac-sodium (N6+ 2.4-D2 mg/L + CH 0.6 g/L + Pro 0.5 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.6 mu mol/L), and dark cultured for 30-50 days at 30 ℃ to obtain the resistant callus through screening.

Example 6 Bispyribac-pCA L Sm2 genetic transformation System-Screen (2)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after co-culturing for 3 days, the callus is washed for 5-6 times, transferred to a culture medium containing bispyribac-sodium resistance selection (N6+ 2.4-D2.5 mg/L + CH 0.8-1 g/L + Pro 0.8 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.25 mu mol/L), and subjected to dark culture at 30 ℃ for 30-50 days to obtain resistant callus through selection.

Example 7 Bispyribac-pCA L Sm2 genetic transformation System-Screen (3)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of the rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after the callus is co-cultured for 3 days, the callus is washed for 5-6 times, transferred to a screening medium containing bispyribac-sodium resistance (N6+ 2.4-D2 mg/L + CH 0.6 g/L + Pro 0.8 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.3 mu mol/L), and cultured in the dark at 30 ℃ for 30-50 days.

EXAMPLE 8 Bispyribac-pCA L Sm2 genetic transformation System-Screen (4)

Taking rice as an example, the engineered agrobacterium obtained in example 2 is transformed into calli of rice Zhonghua 11(ZH11) by agrobacterium-mediated genetic transformation, after co-culturing for 3 days, washed 5-6 times, transferred to a selection medium containing bispyribac-sodium resistance (N6+ 2.4-D2 mg/L + CH 0.6 g/L + Pro 0.5 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.4. mu. mol/L), dark cultured for 30-50 days at 30 ℃, and screened to obtain resistant calli (as shown in FIG. 9).

Example 9 Bispyribac-pCA L Sm2 genetic transformation System-Screen (5)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of the rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after the callus is co-cultured for 3 days, the callus is washed for 5 to 6 times, transferred to a culture medium containing bispyribac-sodium resistance selection (N6+ 2.4-D2 mg/L + CH 0.8 g/L + Pro 0.5 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.5 mu mol/L), and dark cultured for 30 to 50 days at 30 ℃ to obtain the resistant callus through selection.

EXAMPLE 10 Bispyribac-pCA L Sm2 genetic transformation System-Screen (6)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after co-culturing for 3 days, the callus is washed for 5-6 times, transferred to a culture medium containing bispyribac-sodium resistance selection (N6+ 2.4-D2.5 mg/L + CH 0.6 g/L + Pro 0.5 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac-sodium 0.8 mu mol/L), and dark cultured for 30-50 days at 30 ℃ to obtain resistant callus through selection.

EXAMPLE 11 Bispyribac-pCA L Sm2 genetic transformation System-Screen (7)

Taking rice as an example, the engineering agrobacterium obtained in the example 2 is used for transforming the callus of the rice Zhonghua 11(ZH11) by an agrobacterium-mediated genetic transformation method, after the callus is co-cultured for 3 days, the callus is washed for 5 to 6 times, transferred to a culture medium containing bispyribac resistance selection (N6+ 2.4-D2.5 mg/L + CH 0.6 g/L + Pro 0.5 g/L + sucrose 30 g/L + Phytagel 3 g/L + Cn 500 mg/L + bispyribac 1 mu mol/L), and dark cultured for 30 to 50 days at 30 ℃ to obtain the resistant callus through selection.

Example 12 pCA L Sm2 genetic transformation System-screening statistics

As a result of comparison of the positive rates of screening using bispyribac-sodium at different concentrations in examples 5 to 11 (see Table 1), it was found that more than 40% of positive calli were obtained when 0.3 to 0.4. mu. mol/L bispyribac-sodium was added to the screening medium, that the positive callus rate was decreased when the screening pressure was added at a low concentration, and that the positive callus rate was decreased when the screening pressure was added at a high concentration, presumably because the calli were completely inhibited with the increase in the screening pressure and thus positive calli could not be obtained, and therefore, it was found that it was preferable to add 0.3 to 0.4. mu. mol/L bispyribac-sodium to the screening medium, and it was more preferable to add 0.4. mu. mol/L bispyribac-sodium to obtain a good screening efficiency.

TABLE 1 statistics of screening results for bispyribac-sodium at different concentrations

Example 13 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (1)

Transferring the obtained resistant callus to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + bifenox 0.05 mu mol/L), and differentiating for 25-30d to obtain a positive seedling.

EXAMPLE 14 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (2)

The obtained resistant calli were transferred to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + bispyribac-0.1. mu. mol/L) and differentiated for 25-30d to obtain positive shoots (FIG. 10).

Example 15 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (3)

Transferring the obtained resistant callus to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + bifenox 0.25 mu mol/L), and differentiating for 25-30d to obtain a positive seedling.

Example 16 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (4)

Transferring the obtained resistant callus to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + bifenox 0.5 mu mol/L), and differentiating for 25-30d to obtain a positive seedling.

Example 17 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (5)

Transferring the obtained resistant callus to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + bifenox 0.8 mu mol/L), and differentiating for 25-30d to obtain a positive seedling.

Example 18 Bispyribac-pCA L Sm2 genetic transformation System-differentiation (6)

Transferring the obtained resistant callus to a bifenox-resistant differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + bispyribac-1 mu mol/L), and differentiating for 25-30d to obtain a positive seedling.

EXAMPLE 19 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (1)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 25 μ g/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 20 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (2)

The obtained resistant calli were transferred to a differentiating medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + Imazapyr 50. mu.g/L) containing resistance to Imazapyr, and differentiated for 25-30d to obtain positive seedlings (FIG. 10).

Example 21 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (3)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 100 mu g/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 22 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (4)

Transferring the obtained resistant callus to a differentiating culture medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 250 mug/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 23 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (5)

Transferring the obtained resistant callus to a differentiating culture medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 375 mu g/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 24 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (6)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 500 mug/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 25 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (7)

Transferring the obtained resistant callus to a differentiating culture medium (MS + KT 2 mg/L + NAA0.5 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 800 mu g/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 26 Imazapyr-pCA L Sm2 genetic transformation System-differentiation (8)

Transferring the obtained resistant callus to a differentiating culture medium (MS + KT 2 mg/L + NAA0.5 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazapyr 1000 mu g/L) containing imazapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 27 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (1)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 25 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 28 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (2)

The obtained resistant calli were transferred to an imazethapyr resistant differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 50. mu.g/L) and differentiated for 25-30d to obtain positive shoots (FIG. 10).

Example 29 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (3)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA2 mg/L + sorbitol 30 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 100 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 30 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (4)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 250 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 31 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (5)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 375 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 32 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (6)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA1 mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 500 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 33 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (7)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA0.5mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 800 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 34 Imidazovinic acid-pCA L Sm2 genetic transformation System-differentiation (8)

Transferring the obtained resistant callus to a differentiation medium (MS + KT 2 mg/L + NAA0.5mg/L + sorbitol 20 g/L + sucrose 30 g/L + Phytagel 3 g/L + imazethapyr 1000 mu g/L) containing imazethapyr resistance, and differentiating for 25-30d to obtain a positive seedling.

Example 35 pCA L Sm2 genetic transformation System-statistics of differentiation

The comparison of the emergence rates of differentiation cultures with the different concentrations of bispyribac-sodium, imazapyr and imazethapyr added in examples 13-18, 19-26 and 27-34 (see tables 2, 3 and 4) shows that the addition of bispyribac-sodium, imazapyr or imazethapyr to the differentiation medium can inhibit the callus differentiation of ZH11, while the transgene positive callus has a higher differentiation rate, so that the addition of 0.05-0.25. mu. mol/L bispyribac, 30-100. mu.g/L imazapyr or 30-100. mu.g/L imazethapyr to the differentiation medium is preferred, and the addition of 0.1. mu. mol/L bispyribac, 50. mu.g/L imazethapyr or 50. mu.g/L imazethapyr can achieve a good differentiation efficiency when non-transgenosis is inhibited.

TABLE 2 statistics of the differentiation results of bispyribac-sodium at different concentrations

TABLE 3 statistics of differentiation results for imazapyr at different concentrations

TABLE 4 statistics of differentiation results for various concentrations of imazethapyr

In tables 2, 3 and 4, MSRe represents a differentiation medium without a screening agent, the components of the medium are shown in the summary of the invention, BS represents bispyribac-sodium, and BS0.05 represents the addition of bispyribac-sodium of 0.05 mu mol/L.

Example 36 Bispyribac-pCA L Sm2 genetic transformation System-rooting (1)

Transferring the positive seedlings obtained by differentiation to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.05 mu mol/L), and finally obtaining positive transgenic plants.

Example 37 Bispyribac-pCA L Sm2 genetic transformation System-rooting (2)

The positive seedlings obtained by differentiation were transferred to rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.1. mu. mol/L), and finally positive transgenic plants were obtained (FIG. 11).

Example 38 Bispyribac-pCA L Sm2 genetic transformation System-rooting (3)

Transferring the positive seedlings obtained by differentiation to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.2 mu mol/L), and finally obtaining positive transgenic plants.

Example 39 Bispyribac-sodium L Sm2 genetic transformation System-rooting (4)

Transferring the positive seedlings obtained by differentiation to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.3 mu mol/L), and finally obtaining positive transgenic plants.

Example 40 Bispyribac-pCA L Sm2 genetic transformation System-rooting (5)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.4 mu mol/L), and finally positive transgenic plants are obtained.

Example 41 Bispyribac-pCA L Sm2 genetic transformation System-rooting (6)

Transferring the positive seedlings obtained by differentiation to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + bispyribac-sodium 0.5 mu mol/L), and finally obtaining positive transgenic plants.

Example 42 Bispyribac-sodium L Sm2 genetic transformation System-rooting (7)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + bispyribac-sodium 1 mu mol/L), and finally positive transgenic plants are obtained.

Example 43 Bispyribac-sodium L Sm2 genetic transformation System-rooting (8)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + bispyribac-sodium 3 mu mol/L), and finally positive transgenic plants are obtained.

Example 44 Bispyribac-pCA L Sm2 genetic transformation System-rooting (9)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + bispyribac-sodium 5 mu mol/L), and finally positive transgenic plants are obtained.

Example 45 Bispyribac-pCA L Sm2 genetic transformation System-rooting (10)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing bispyribac-sodium resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + bispyribac-sodium 10 mu mol/L), and finally positive transgenic plants are obtained.

Example 46 Imazapyr-pCA L Sm2 genetic transformation System-rooting (1)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazapyr 25 mug/L), and finally positive transgenic plants are obtained.

Example 47 Imazapyr-pCA L Sm2 genetic transformation System-rooting (2)

The positive seedlings obtained by differentiation were transferred to rooting medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazapyr 50. mu.g/L), and finally positive transgenic plants were obtained (FIG. 11).

Example 48 Imazapyr-pCA L Sm2 genetic transformation System-rooting (3)

The positive seedlings obtained by differentiation are transferred to a rooting medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazapyr 100 mu g/L), and finally positive transgenic plants are obtained.

Example 49 Imazapyr-pCA L Sm2 genetic transformation System-rooting (4)

The positive seedlings obtained by differentiation are transferred to a rooting culture medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazapyr 250 mu g/L), and finally positive transgenic plants are obtained.

Example 50 Imazapyr-pCA L Sm2 genetic transformation System-rooting (5)

The positive seedlings obtained by differentiation are transferred to a rooting culture medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazapyr 375 mu g/L), and finally positive transgenic plants are obtained.

Example 51 Imazapyr-pCA L Sm2 genetic transformation System-rooting (6)

The positive seedlings obtained by differentiation are transferred to a rooting culture medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazapyr 500 mu g/L), and finally positive transgenic plants are obtained.

Example 52 Imazapyr-pCA L Sm2 genetic transformation System-rooting (7)

The positive seedlings obtained by differentiation are transferred to a rooting culture medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + imazapyr 625 mu g/L), and finally positive transgenic plants are obtained.

Example 53 Imazapyr-pCA L Sm2 genetic transformation System-rooting (8)

The positive seedlings obtained by differentiation are transferred to a rooting culture medium containing imazapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + imazapyr 1000 mu g/L), and finally positive transgenic plants are obtained.

Example 54 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (1)

The positive seedlings obtained by differentiation are transferred to rooting culture medium (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazethapyr 25 mug/L) containing imazethapyr resistance, and finally positive transgenic plants are obtained.

Example 55 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (2)

The positive seedlings obtained by differentiation were transferred to rooting medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazethapyr 50. mu.g/L), and finally positive transgenic plants were obtained (FIG. 11).

Example 56 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (3)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 1 mg/L + Phytagel 3 g/L + imazethapyr 100 mu g/L), and finally positive transgenic plants are obtained.

Example 57 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (4)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazethapyr 250 mu g/L), and finally positive transgenic plants are obtained.

Example 58 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (5)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazethapyr 375 mu g/L), and finally positive transgenic plants are obtained.

Example 59 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (6)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.5 mg/L + Phytagel 3 g/L + imazethapyr 500 mu g/L), and finally positive transgenic plants are obtained.

Example 60 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (7)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + imazethapyr 625 mu g/L), and finally positive transgenic plants are obtained.

Example 61 Imidazovinic acid-pCA L Sm2 genetic transformation System-rooting (8)

The positive seedlings obtained by differentiation are transferred to rooting culture medium containing imazethapyr resistance (1/2MS + sucrose 20 g/L + paclobutrazol 0.8 mg/L + Phytagel 3 g/L + imazethapyr 1000 mug/L), and finally positive transgenic plants are obtained.

Example 62 pCA L Sm2 genetic transformation System-rooting statistics

The comparison of the rooting survival rates of rooting cultures with the bispyribac-sodium, imazapyr and imazethapyr added in different concentrations in examples 36-45, 46-53 and 54-61 (see tables 5,6 and 7) shows that the rooting culture medium added with 0.05-10 μmol/L bispyribac or 25-1000 μ g/L imazapyr or 25-1000 μ g/L imazethapyr can inhibit the survival of differentiated seedlings of ZH11, while the survival rate of most transgenic positive differentiated seedlings reaches more than 80% respectively.

TABLE 5 Bispyribac-sodium rooting results statistics for different concentrations

TABLE 6 statistics of rooting results for imazapyr of different concentrations

TABLE 7 statistics of rooting results for imazethapyr at different concentrations

Example 63 transgenic line identification

In order to identify whether the obtained line is a transgenic line, this example performed PCR verification of a partially positive transgenic plant obtained by screening culture, differentiation culture and rooting culture.

Firstly, extracting sample DNA, the DNA extraction step is that rice leaves with the length of about 2cm are placed in a 2ml centrifuge tube, 800 mul of 1.5 × CTAB is added into a mortar, the leaves are ground to be homogenized and poured back into the centrifuge tube, water bath at 65 ℃ is carried out for 20-30min, the mixture is evenly mixed for 1 time every 5min, centrifugation is carried out at 12000rpm for 10min, 400 mul of supernatant is absorbed into a new centrifuge tube, 2 times of absolute ethyl alcohol with ice precooling by volume is added, ice is placed at 20 ℃ for 20min, centrifugation is carried out at 12000rpm for 10min, supernatant is abandoned, 500 mul of 75 percent ethyl alcohol is added, the mixture is reversely rinsed, centrifugation is carried out at 8000rpm for 5min, the supernatant is abandoned, the mixture is placed on a super clean bench to be dried by blowing₂O dissolves the DNA.

In order to distinguish endogenous genes of rice, a pair of primers (0310-F4/0310-R4) is designed to carry out PCR amplification detection on a genomic DNA sample of a transgenic strain, the primers cannot amplify a fragment by taking the endogenous rice genome as a template, and the size of the fragment amplified by taking a transgenic expression cassette as the template is about 670 bp.

The primer sequences are as follows:

0310-F4:CATTGAGAACCTCCCTGTG(SEQ ID NO.13)；

0310-R4:GACAAATTTGTTTGTCAGATCAA(SEQ ID NO.14)。

plasmid DNA for transformation was used as a positive control, and ZH11 genomic DNA was used as a negative control.

The PCR reaction procedure was as follows: pre-denaturation at 94 deg.C for 5min, denaturation at 94 deg.C for 45s, and annealing at 55-65 deg.C for 45 s; extending for 1.5min at 72 ℃; 30-35 cycles; further extension for 10min at 72 ℃; and finishing at 16 ℃.

The PCR reaction system is as follows:

the PCR product was electrophoresed on an agarose gel, and the results are shown in FIG. 12. Electrophoresis results show that most of transgenic samples contain about 670bp of transgenic bands, and the sizes of the transgenic bands are the same as those of the vector control; while the negative control ZH11 failed to produce a band.

Example 64 resistance phenotype identification

Selecting part of rooting material, transplanting for 7-14 days (about 3-5 leaf stage), spraying 90mg/m²Bispyribac-sodium (a, b of FIG. 13). After 3-7 days of spraying, the wild type has withered and yellow leaves. After 7 days, the wild-type control ZH11 had died of yellow, and most plants of the transgenic lines grew normally, with yellowing appearing in part. After 14 days, the wild-type control ZH11 and the transgenic sensitive line had completely died, and the surviving line was the bispyribac-sodium resistant line (c, d of FIG. 13).

After a part of rooting materials are selected and transplanted for 7-14 days (about 3-5 leaf stage), 196 mg/L imazapyr (e in figure 13) is sprayed, after 21 days, wild type control ZH11, 9311 or MH63 shows withered yellow, withered or dead to different degrees, but the transgenic positive line grows normally, and the survival line is an imazapyr resistant line (f in figure 13).

After a part of rooting materials are selected and transplanted for 7-14 days (about 3-5 leaf stage), 1500 mg/L imazethapyr (g in figure 13) is sprayed, after 21 days, wild type control ZH11, 9311 or MH63 shows withered yellow, withered or dead to different degrees, but the transgenic positive line grows normally, and the survival line is an imazethapyr resistant line (h in figure 13).

The results show that the transgenic line obtained by screening has high resistance to bispyribac-sodium, imazapyr and imazethapyr. The three herbicides are only representatives of the herbicide classes, and the obtained transgenic line not only has high resistance of the three herbicides, but also has high resistance of other sulfonylurea herbicides, imidazolinones herbicides and pyrimidine salicylic acid herbicides such as bensulfuron-methyl, chlorsulfuron, pyrithiobac-sodium and the like.

The results show that the application successfully establishes a genetic transformation full-term screening system based on the bispyribac-sodium/imazapyr/imazethapyr-A L Sm2 screening marker, and can be used for rice genetic transformation.

The pCA L Sm2 obtained by the invention is used as a plant binary expression vector, and can enter the vector through cloning other expression cassettes to carry out genetic transformation to obtain corresponding characters, such as a fluorescent protein expression cassette, a GUS reporter gene expression cassette, an insect-resistant expression cassette, an herbicide-resistant expression cassette, other functional genes and the like.

Although the invention has been described in detail hereinabove with respect to a general description and specific embodiments thereof, it will be apparent to those skilled in the art that modifications or improvements may be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.

Sequence listing

<110> Hainan Borax Rice Gene science and technology Co., Ltd

<120> rice A L S mutant gene, plant transgenic screening vector pCA L Sm2 containing gene and application thereof

<130>KHP201110923.9

<160>14

<170>SIPOSequenceListing 1.0

<210>1

<211>644

<212>PRT

<213> Artificial Sequence (Artificial Sequence)

<400>1

Met Ala Thr Thr Ala Ala Ala Ala Ala Ala Ala Leu Ser Ala Ala Ala

1 5 10 15

Thr Ala Lys Thr Gly Arg Lys Asn His Gln Arg His His Val Leu Pro

20 25 30

Ala Arg Gly Arg Val Gly Ala Ala Ala Val Arg Cys Ser Ala Val Ser

35 40 45

Pro Val Thr Pro Pro Ser Pro Ala Pro Pro Ala Thr Pro Leu Arg Pro

50 55 60

Trp Gly Pro Ala Glu Pro Arg Lys Gly Ala Asp Ile Leu Val Glu Ala

65 70 75 80

Leu Glu Arg Cys Gly Val Ser Asp Val Phe Ala Tyr Pro Gly Ala Ala

85 90 95

Ser Met Glu Ile His Gln Ala Leu Thr Arg Ser Pro Val Ile Thr Asn

100 105 110

His Leu Phe Arg His Glu Gln Gly Glu Ala Phe Ala Ala Ser Gly Tyr

115 120 125

Ala Arg Ala Ser Gly Arg Val Gly Val Cys Val Ala Thr Ser Gly Pro

130 135140

Gly Ala Thr Asn Leu Val Ser Ala Leu Ala Asp Ala Leu Leu Asp Ser

145 150 155 160

Val Pro Met Val Ala Ile Thr Gly Gln Val Pro Arg Arg Met Ile Gly

165 170 175

Thr Asp Ala Phe Gln Glu Thr Pro Ile Val Glu Val Thr Arg Ser Ile

180 185 190

Thr Lys His Asn Tyr Leu Val Leu Asp Val Glu Asp Ile Pro Arg Val

195 200 205

Ile Gln Glu Ala Phe Phe Leu Ala Ser Ser Gly Arg Pro Gly Pro Val

210 215 220

Leu Val Asp Ile Pro Lys Asp Ile Gln Gln Gln Met Ala Val Pro Val

225 230 235 240

Trp Asp Thr Ser Met Asn Leu Pro Gly Tyr Ile Ala Arg Leu Pro Lys

245 250 255

Pro Pro Ala Thr Glu Leu Leu Glu Gln Val Leu Arg Leu Val Gly Glu

260 265 270

Ser Arg Arg Pro Ile Leu Tyr Val Gly Gly Gly Cys Ser Ala Ser Gly

275 280 285

Asp Glu Leu Arg Trp Phe Val Glu Leu Thr Gly Ile Pro Val Thr Thr

290 295 300

Thr Leu Met Gly Leu Gly Asn Phe Pro Ser Asp Asp Pro Leu Ser Leu

305 310 315 320

Arg Met Leu Gly Met His Gly Thr Val Tyr Ala Asn Tyr Ala Val Asp

325 330 335

Lys Ala Asp Leu Leu Leu Ala Phe Gly Val Arg Phe Asp Asp Arg Val

340 345 350

Thr Gly Lys Ile Glu Ala Phe Ala Ser Arg Ala Lys Ile Val His Ile

355 360 365

Asp Ile Asp Pro Ala Glu Ile Gly Lys Asn Lys Gln Pro His Val Ser

370 375 380

Ile Cys Ala Asp Val Lys Leu Ala Leu Gln Gly Leu Asn Ala Leu Leu

385 390 395 400

Gln Gln Ser Thr Thr Lys Thr Ser Ser Asp Phe Ser Ala Trp His Asn

405 410 415

Glu Leu Asp Gln Gln Lys Arg Glu Phe Pro Leu Gly Tyr Lys Thr Phe

420 425 430

Gly Glu Glu Ile Pro Pro Gln Tyr Ala Ile Gln Val Leu Asp Glu Leu

435 440 445

Thr Lys Gly Glu Ala Ile Ile Ala Thr Gly Val Gly Gln His Gln Met

450 455 460

Trp Ala Ala Gln Tyr Tyr Thr Tyr Lys Arg Pro Arg Gln Trp Leu Ser

465 470 475 480

Ser Ala Gly Leu Gly Ala Met Gly Phe Gly Leu Pro Ala Ala Ala Gly

485 490 495

Ala Ser Val Ala Asn Pro Gly Val Thr Val Val Asp Ile Asp Gly Asp

500 505 510

Gly Ser Phe Leu Met Asn Ile Gln Glu Leu Ala Leu Ile Arg Ile Glu

515 520 525

Asn Leu Pro Val Lys Val Met Val Leu Asn Asn Gln His Leu Gly Met

530 535 540

Val Val Gln Leu Glu Asp Arg Phe Tyr Lys Ala Asn Arg Ala His Thr

545 550 555 560

Tyr Leu Gly Asn Pro Glu Cys Glu Ser Glu Ile Tyr Pro Asp Phe Val

565 570 575

Thr Ile Ala Lys Gly Phe Asn Ile Pro Ala Val Arg Val Thr Lys Lys

580 585 590

Ser Glu Val Arg Ala Ala Ile Lys Lys Met Leu Glu Thr Pro Gly Pro

595 600 605

Tyr Leu Leu Asp Ile Ile Val Pro His Gln Glu His Val Leu Pro Met

610 615 620

Ile Pro Ile Gly Gly Ala Phe Lys Asp Met Ile Leu Asp Gly Asp Gly

625 630 635 640

Arg Thr Val Tyr

<210>2

<211>1935

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>2

atggctacga ccgccgcggc cgcggccgcc gccctgtccg ccgccgcgac ggccaagacc 60

ggccgtaaga accaccagcg acaccacgtc cttcccgctc gaggccgggt gggggcggcg 120

gcggtcaggt gctcggcggt gtccccggtc accccgccgt ccccggcgcc gccggccacg 180

ccgctccggc cgtgggggcc ggccgagccc cgcaagggcg cggacatcct cgtggaggcg 240

ctggagcggt gcggcgtcag cgacgtgttc gcctacccgg gcgccgcgtc catggagatc 300

caccaggcgc tgacgcgctc cccggtcatc accaaccacc tcttccgcca cgagcagggc 360

gaggcgttcg cggcgtccgg gtacgcgcgc gcgtccggcc gcgtcggggt ctgcgtcgcc 420

acctccggcc ccggggcaac caacctcgtg tccgcgctcg ccgacgcgct gctcgactcc 480

gtcccgatgg tcgccatcac gggccaggtc ccccgccgca tgatcggcac cgacgccttc 540

caggagacgc ccatagtcga ggtcacccgc tccatcacca agcacaatta ccttgtcctt 600

gatgtggagg acatcccccg cgtcatacag gaagccttct tcctcgcgtc ctcgggccgt 660

cctggcccgg tgctggtcga catccccaag gacatccagc agcagatggc cgtgccggtc 720

tgggacacct cgatgaatct accagggtac atcgcacgcc tgcccaagcc acccgcgaca 780

gaattgcttg agcaggtctt gcgtctggtt ggcgagtcac ggcgcccgat tctctatgtc 840

ggtggtggct gctctgcatc tggtgacgaa ttgcgctggt ttgttgagct gactggtatc 900

ccagttacaa ccactctgat gggcctcggc aatttcccca gtgacgaccc gttgtccctg 960

cgcatgcttg ggatgcatgg cacggtgtac gcaaattatg ccgtggataa ggctgacctg 1020

ttgcttgcgt ttggtgtgcg gtttgatgat cgtgtgacag ggaaaattga ggcttttgca 1080

agcagggcca agattgtgca cattgacatt gatccagcag agattggaaa gaacaagcaa 1140

ccacatgtgt caatttgcgc agatgttaag cttgctttac agggcttgaa tgctctgcta 1200

caacagagca caacaaagac aagttctgat tttagtgcat ggcacaatga gttggaccag 1260

cagaagaggg agtttcctct ggggtacaaa acttttggtg aagagatccc accgcaatat 1320

gccattcagg tgctggatga gctgacgaaa ggtgaggcaa tcatcgctac tggtgttggg 1380

cagcaccaga tgtgggcggc acaatattac acctacaagc ggccacggca gtggctgtct 1440

tcggctggtc tgggcgcaat gggatttggg ctgcctgctg cagctggtgc ttctgtggct 1500

aacccaggtg tcacagttgt tgatattgat ggggatggta gcttcctcat gaacattcag 1560

gagctggcat tgatccgcat tgagaacctc cctgtgaagg tgatggtgtt gaacaaccaa 1620

catttgggta tggtggtgca attggaggat aggttttaca aggcgaatag ggcgcataca 1680

tacttgggca acccggaatg tgagagcgag atatatccag attttgtgac tattgctaag 1740

gggttcaata ttcctgcagt ccgtgtaaca aagaagagtg aagtccgtgc cgccatcaag 1800

aagatgctcg agactccagg gccatacttg ttggatatca tcgtcccgca ccaggagcat 1860

gtgctgccta tgatcccaat tgggggcgca ttcaaggaca tgatcctgga tggtgatggc 1920

aggactgtgt attaa 1935

<210>3

<211>4431

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>3

cgtaaagtct tcactcctcc ccctttctct ctagttagcg gagacatgac aaccagtcat 60

ccgattaggt ttatagtggc attgcaagca gtcagcaaat gaataaatga aagaggcaat 120

cttcatggtc ctcttcatct tgtctcacat gcgagttgat tttagaccaa cacggtaact 180

caggggataa aatagatttg ttacaaattt ccaataagta agattccatg aaattggtga 240

tagtatataa tgattttatt gcacaagcta tgcattgcag ctactgattc aacactattc 300

agaaaaaaaa agaacaagtg tatttctggt aaaactgttc cattcaaaat ctagtccacg 360

actagtccat gatttggtcg tgtgaaaaca atggatgcac tatatagtct ctagtactat 420

tctattgtac taagcactat atatagtatt ataaactacg gtttatggag tagccagcaa 480

gacaataagt taacaagaaa taaatttaaa gtactaaaca caataagcca attagcatgg 540

tgaaatgatg atttgctatg actaatctac gactaattgt gcgacttgct atttggtcga 600

gtcgtagccc tctagtcgtc tgacttgact gacgttatga ctagtctacg acttgataac 660

agcgatccag atgtcttaag tgatgaggag aagaaagaac taccagaaag taaaccttat 720

atgcatagtt acatacacag gtacacttcc gaaggcccca atcaatggaa taccatatgc 780

tcttattagg ctattatatg gttctgggta acaattaaat atatcatggg tgtaccgcca 840

atgtgaaatt gagaactgca tacacatagc cacattataa aatataaatg cactatgctc 900

ctgatcatgg aatgccaacc ccttattatc aaacccaaag aagggaaatc cctttctatc 960

tcaagcatgc acaattacct ttgtttagca taaatctatc aaatattgca atgcaaacct 1020

taagcacaga tgtcctccct cttaaatatt aatcataatc ctcagtaaat ggacatacag 1080

cataaagtac tttaaattac cataggttga attggaaata ttctttttag tagctcacag 1140

aaaaatgggt actaaaacta actattagta aacataaaag ccccttaatg ataggagggc 1200

tctacacaag acagtcagta gcatgataac cacctacaat gttgttccta caaataaaaa 1260

tactgtagca atctcttact aagttaaaac atactgaggt tctagggttt aaccataagt 1320

aattagaata tcaaaatagc tcaagattag agaaggtcct acagaaaaac acggttatct 1380

gcttctcaaa tggcctagct acaccgggca ctagcaggat cttaaacagc actaaaataa 1440

gtatctccct tggtcatcaa atcgaaaaga aaatcctaca gagtccacgc ctttccttcc 1500

ccccactaat taacgaaaag aaacgcagag ttccaattaa ggagaaagag atacggggta 1560

caacaaacat cgcattcgtc tcgtgctagg gttttcggga ggcgggtcta gggttgaggc 1620

aaaaaggggg agggaattga gcagggggtt accgcggtag tcgacgccgg agttgagctt 1680

gacgacgacg gggcgccccc tgatggactt gaggaagtcg gagggcgtct tcaccgcccc 1740

gccgccgccg ccaccgccgc cgccgcccga gccggacttc tcgccgccac tgctcatctt 1800

gcgctgcgtt tgtgcgggtg cgggtgcggg tgctagactg ctaggtctcg cggttgcatc 1860

cgcatccgac tttgagatcg attttttatc gggttctgta ccctccaccc gttattggga 1920

ctgacccacc tgtcatcctc atccaatcga ctgacacgcg ggcccagatc gaccccgacg 1980

tggctgtgtg tcatcctatc ccaccgacat atggggccca ctgtgacgtg gccccacacg 2040

atcccatccg agccacacat cgcctcacgc tgcgtcaccg cgcgcggaca aaacacccac 2100

acccccacac tctccacccc tctctccctc tcgcccaaac ccagaaaccc tcgccgccgc 2160

cgccgccgcc accacccacc atggctacga ccgccgcggc cgcggccgcc gccctgtccg 2220

ccgccgcgac ggccaagacc ggccgtaaga accaccagcg acaccacgtc cttcccgctc 2280

gaggccgggt gggggcggcg gcggtcaggt gctcggcggt gtccccggtc accccgccgt 2340

ccccggcgcc gccggccacg ccgctccggc cgtgggggcc ggccgagccc cgcaagggcg 2400

cggacatcct cgtggaggcg ctggagcggt gcggcgtcag cgacgtgttc gcctacccgg 2460

gcgccgcgtc catggagatc caccaggcgc tgacgcgctc cccggtcatc accaaccacc 2520

tcttccgcca cgagcagggc gaggcgttcg cggcgtccgg gtacgcgcgc gcgtccggcc 2580

gcgtcggggt ctgcgtcgcc acctccggcc ccggggcaac caacctcgtg tccgcgctcg 2640

ccgacgcgct gctcgactcc gtcccgatgg tcgccatcac gggccaggtc ccccgccgca 2700

tgatcggcac cgacgccttc caggagacgc ccatagtcga ggtcacccgc tccatcacca 2760

agcacaatta ccttgtcctt gatgtggagg acatcccccg cgtcatacag gaagccttct 2820

tcctcgcgtc ctcgggccgt cctggcccgg tgctggtcga catccccaag gacatccagc 2880

agcagatggc cgtgccggtc tgggacacct cgatgaatct accagggtac atcgcacgcc 2940

tgcccaagcc acccgcgaca gaattgcttg agcaggtctt gcgtctggtt ggcgagtcac 3000

ggcgcccgattctctatgtc ggtggtggct gctctgcatc tggtgacgaa ttgcgctggt 3060

ttgttgagct gactggtatc ccagttacaa ccactctgat gggcctcggc aatttcccca 3120

gtgacgaccc gttgtccctg cgcatgcttg ggatgcatgg cacggtgtac gcaaattatg 3180

ccgtggataa ggctgacctg ttgcttgcgt ttggtgtgcg gtttgatgat cgtgtgacag 3240

ggaaaattga ggcttttgca agcagggcca agattgtgca cattgacatt gatccagcag 3300

agattggaaa gaacaagcaa ccacatgtgt caatttgcgc agatgttaag cttgctttac 3360

agggcttgaa tgctctgcta caacagagca caacaaagac aagttctgat tttagtgcat 3420

ggcacaatga gttggaccag cagaagaggg agtttcctct ggggtacaaa acttttggtg 3480

aagagatccc accgcaatat gccattcagg tgctggatga gctgacgaaa ggtgaggcaa 3540

tcatcgctac tggtgttggg cagcaccaga tgtgggcggc acaatattac acctacaagc 3600

ggccacggca gtggctgtct tcggctggtc tgggcgcaat gggatttggg ctgcctgctg 3660

cagctggtgc ttctgtggct aacccaggtg tcacagttgt tgatattgat ggggatggta 3720

gcttcctcat gaacattcag gagctggcat tgatccgcat tgagaacctc cctgtgaagg 3780

tgatggtgtt gaacaaccaa catttgggta tggtggtgca attggaggat aggttttaca 3840

aggcgaatag ggcgcataca tacttgggca acccggaatg tgagagcgag atatatccag 3900

attttgtgac tattgctaag gggttcaata ttcctgcagt ccgtgtaaca aagaagagtg 3960

aagtccgtgc cgccatcaag aagatgctcg agactccagg gccatacttg ttggatatca 4020

tcgtcccgca ccaggagcat gtgctgccta tgatcccaat tgggggcgca ttcaaggaca 4080

tgatcctgga tggtgatggc aggactgtgt attaatctag agtcctcagc catagagctg 4140

ctgctgttct agggttcaca agtctgccta tttgtcttcc ccaatggagc tatggttgtc 4200

tggtctggtc cttggtcgtg tcccgtttca ttgtgtacta tttacctgta atgtgtatcc 4260

ttaagtctgg tttgatggtg tctgaaacgt tttgctgtgg tagagcagca tggaagaact 4320

ataatgaata agtgatccct aatcattgtg tccaaatttt gcttctgcta tacccttttg 4380

tgctgtttct tatgttttgc ttaaaaattt gatctgacaa acaaatttgt c 4431

<210>4

<211>10933

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>4

ctgcaggccc gggcagcgct gaagaacttc cctaggcacg tgtacgtatt ttttaccagg 60

tgaactccaa gtcctggacc cttttttaag cttagattgt cgtttcccgc cttcagttta 120

aactatcagt gtttgacagg atatattggc gggtaaacct aagagaaaag agcgtttatt 180

agaataacgg atatttaaaa gggcgtgaaa aggtttatcc gttcgtccat ttgtatgtgc 240

atgccaacca cagggttccc ctcgggatca aagtactttg atccaacccc tccgctgcta 300

tagtgcagtc ggcttctgac gttcagtgca gccgtcttct gaaaacgaca tgtcgcacaa 360

gtcctaagtt acgcgacagg ctgccgccct gcccttttcc tggcgttttc ttgtcgcgtg 420

ttttagtcgc ataaagtaga atacttgcga ctagaaccgg agacattacg ccatgaacaa 480

gagcgccgcc gctggcctgc tgggctatgc ccgcgtcagc accgacgacc aggacttgac 540

caaccaacgg gccgaactgc acgcggccgg ctgcaccaag ctgttttccg agaagatcac 600

cggcaccagg cgcgaccgcc cggagctggc caggatgctt gaccacctac gccctggcga 660

cgttgtgaca gtgaccaggc tagaccgcct ggcccgcagc acccgcgacc tactggacat 720

tgccgagcgc atccaggagg ccggcgcggg cctgcgtagc ctggcagagc cgtgggccga 780

caccaccacg ccggccggcc gcatggtgtt gaccgtgttc gccggcattg ccgagttcga 840

gcgttcccta atcatcgacc gcacccggag cgggcgcgag gccgccaagg cccgaggcgt 900

gaagtttggc ccccgcccta ccctcacccc ggcacagatc gcgcacgccc gcgagctgat 960

cgaccaggaa ggccgcaccg tgaaagaggc ggctgcactg cttggcgtgc atcgctcgac 1020

cctgtaccgc gcacttgagc gcagcgagga agtgacgccc accgaggcca ggcggcgcgg 1080

tgccttccgt gaggacgcat tgaccgaggc cgacgccctg gcggccgccg agaatgaacg 1140

ccaagaggaa caagcatgaa accgcaccag gacggccagg acgaaccgtt tttcattacc 1200

gaagagatcg aggcggagat gatcgcggcc gggtacgtgt tcgagccgcc cgcgcacgtc 1260

tcaaccgtgc ggctgcatga aatcctggcc ggtttgtctg atgccaagct ggcggcctgg 1320

ccggccagct tggccgctga agaaaccgag cgccgccgtc taaaaaggtg atgtgtattt 1380

gagtaaaaca gcttgcgtca tgcggtcgct gcgtatatga tgcgatgagt aaataaacaa 1440

atacgcaagg ggaacgcatg aaggttatcg ctgtacttaa ccagaaaggc gggtcaggca 1500

agacgaccat cgcaacccat ctagcccgcg ccctgcaact cgccggggcc gatgttctgt 1560

tagtcgattc cgatccccag ggcagtgccc gcgattgggc ggccgtgcgg gaagatcaac 1620

cgctaaccgt tgtcggcatc gaccgcccga cgattgaccg cgacgtgaag gccatcggcc 1680

ggcgcgactt cgtagtgatc gacggagcgc cccaggcggc ggacttggct gtgtccgcga 1740

tcaaggcagc cgacttcgtg ctgattccgg tgcagccaag cccttacgac atatgggcca 1800

ccgccgacct ggtggagctg gttaagcagc gcattgaggt cacggatgga aggctacaag 1860

cggcctttgt cgtgtcgcgg gcgatcaaag gcacgcgcat cggcggtgag gttgccgagg 1920

cgctggccgg gtacgagctg cccattcttg agtcccgtat cacgcagcgc gtgagctacc 1980

caggcactgc cgccgccggc acaaccgttc ttgaatcaga acccgagggc gacgctgccc 2040

gcgaggtcca ggcgctggcc gctgaaatta aatcaaaact catttgagtt aatgaggtaa 2100

agagaaaatg agcaaaagca caaacacgct aagtgccggc cgtccgagcg cacgcagcag 2160

caaggctgca acgttggcca gcctggcaga cacgccagcc atgaagcggg tcaactttca 2220

gttgccggcg gaggatcaca ccaagctgaa gatgtacgcg gtacgccaag gcaagaccat 2280

taccgagctg ctatctgaat acatcgcgca gctaccagag taaatgagca aatgaataaa 2340

tgagtagatg aattttagcg gctaaaggag gcggcatgga aaatcaagaa caaccaggca 2400

ccgacgccgt ggaatgcccc atgtgtggag gaacgggcgg ttggccaggc gtaagcggct 2460

gggttgtctg ccggccctgc aatggcactg gaacccccaa gcccgaggaa tcggcgtgac 2520

ggtcgcaaac catccggccc ggtacaaatc ggcgcggcgc tgggtgatga cctggtggag 2580

aagttgaagg ccgcgcaggc cgcccagcgg caacgcatcg aggcagaagc acgccccggt 2640

gaatcgtggc aagcggccgc tgatcgaatc cgcaaagaat cccggcaacc gccggcagcc 2700

ggtgcgccgt cgattaggaa gccgcccaag ggcgacgagc aaccagattt tttcgttccg 2760

atgctctatg acgtgggcac ccgcgatagt cgcagcatca tggacgtggc cgttttccgt 2820

ctgtcgaagc gtgaccgacg agctggcgag gtgatccgct acgagcttcc agacgggcac 2880

gtagaggttt ccgcagggcc ggccggcatg gccagtgtgt gggattacga cctggtactg 2940

atggcggttt cccatctaac cgaatccatg aaccgatacc gggaagggaa gggagacaag 3000

cccggccgcg tgttccgtcc acacgttgcg gacgtactca agttctgccg gcgagccgat 3060

ggcggaaagc agaaagacga cctggtagaa acctgcattc ggttaaacac cacgcacgtt 3120

gccatgcagc gtacgaagaa ggccaagaac ggccgcctgg tgacggtatc cgagggtgaa 3180

gccttgatta gccgctacaa gatcgtaaag agcgaaaccg ggcggccgga gtacatcgag 3240

atcgagctag ctgattggat gtaccgcgag atcacagaag gcaagaaccc ggacgtgctg 3300

acggttcacc ccgattactt tttgatcgat cccggcatcg gccgttttct ctaccgcctg 3360

gcacgccgcg ccgcaggcaa ggcagaagcc agatggttgt tcaagacgat ctacgaacgc 3420

agtggcagcg ccggagagtt caagaagttc tgtttcaccg tgcgcaagct gatcgggtca 3480

aatgacctgc cggagtacga tttgaaggag gaggcggggc aggctggccc gatcctagtc 3540

atgcgctacc gcaacctgat cgagggcgaa gcatccgccg gttcctaatg tacggagcag 3600

atgctagggc aaattgccct agcaggggaa aaaggtcgaa aaggtctctt tcctgtggat 3660

agcacgtaca ttgggaaccc aaagccgtac attgggaacc ggaacccgta cattgggaac 3720

ccaaagccgt acattgggaa ccggtcacac atgtaagtga ctgatataaa agagaaaaaa 3780

ggcgattttt ccgcctaaaa ctctttaaaa cttattaaaa ctcttaaaac ccgcctggcc 3840

tgtgcataac tgtctggcca gcgcacagcc gaagagctgc aaaaagcgcc tacccttcgg 3900

tcgctgcgct ccctacgccc cgccgcttcg cgtcggccta tcgcggccgc tggccgctca 3960

aaaatggctg gcctacggcc aggcaatcta ccagggcgcg gacaagccgc gccgtcgcca 4020

ctcgaccgcc ggcgcccaca tcaaggcacc ctgcctcgcg cgtttcggtg atgacggtga 4080

aaacctctga cacatgcagc tcccggagac ggtcacagct tgtctgtaag cggatgccgg 4140

gagcagacaa gcccgtcagg gcgcgtcagc gggtgttggc gggtgtcggg gcgcagccat 4200

gacccagtca cgtagcgata gcggagtgta tactggctta actatgcggc atcagagcag 4260

attgtactga gagtgcacca tatgcggtgt gaaataccgc acagatgcgt aaggagaaaa 4320

taccgcatca ggcgctcttc cgcttcctcg ctcactgact cgctgcgctc ggtcgttcgg 4380

ctgcggcgag cggtatcagc tcactcaaag gcggtaatac ggttatccac agaatcaggg 4440

gataacgcag gaaagaacat gtgagcaaaa ggccagcaaa aggccaggaa ccgtaaaaag 4500

gccgcgttgc tggcgttttt ccataggctc cgcccccctg acgagcatca caaaaatcga 4560

cgctcaagtc agaggtggcg aaacccgaca ggactataaa gataccaggc gtttccccct 4620

ggaagctccc tcgtgcgctc tcctgttccg accctgccgc ttaccggata cctgtccgcc 4680

tttctccctt cgggaagcgt ggcgctttct catagctcac gctgtaggta tctcagttcg 4740

gtgtaggtcg ttcgctccaa gctgggctgt gtgcacgaac cccccgttca gcccgaccgc 4800

tgcgccttat ccggtaacta tcgtcttgag tccaacccgg taagacacga cttatcgcca 4860

ctggcagcag ccactggtaa caggattagc agagcgaggt atgtaggcgg tgctacagag 4920

ttcttgaagt ggtggcctaa ctacggctac actagaagga cagtatttgg tatctgcgct 4980

ctgctgaagc cagttacctt cggaaaaaga gttggtagct cttgatccgg caaacaaacc 5040

accgctggta gcggtggttt ttttgtttgc aagcagcaga ttacgcgcag aaaaaaagga 5100

tctcaagaag atcctttgat cttttctacg gggtctgacg ctcagtggaa cgaaaactca 5160

cgttaaggga ttttggtcat gcattctagg tactaaaaca attcatccag taaaatataa 5220

tattttattt tctcccaatc aggcttgatc cccagtaagt caaaaaatag ctcgacatac 5280

tgttcttccc cgatatcctc cctgatcgac cggacgcaga aggcaatgtc ataccacttg 5340

tccgccctgc cgcttctccc aagatcaata aagccactta ctttgccatc tttcacaaag 5400

atgttgctgt ctcccaggtc gccgtgggaa aagacaagtt cctcttcggg cttttccgtc 5460

tttaaaaaat catacagctc gcgcggatct ttaaatggag tgtcttcttc ccagttttcg 5520

caatccacat cggccagatc gttattcagt aagtaatcca attcggctaa gcggctgtct 5580

aagctattcg tatagggaca atccgatatg tcgatggagt gaaagagcct gatgcactcc 5640

gcatacagct cgataatctt ttcagggctt tgttcatctt catactcttc cgagcaaagg 5700

acgccatcgg cctcactcat gagcagattg ctccagccat catgccgttc aaagtgcagg 5760

acctttggaa caggcagctt tccttccagc catagcatca tgtccttttc ccgttccaca 5820

tcataggtgg tccctttata ccggctgtcc gtcattttta aatataggtt ttcattttct 5880

cccaccagct tatatacctt agcaggagac attccttccg tatcttttac gcagcggtat 5940

ttttcgatca gttttttcaa ttccggtgat attctcattt tagccattta ttatttcctt 6000

cctcttttct acagtattta aagatacccc aagaagctaa ttataacaag acgaactcca 6060

attcactgtt ccttgcattc taaaacctta aataccagaa aacagctttt tcaaagttgt 6120

tttcaaagtt ggcgtataac atagtatcga cggagccgat tttgaaaccg cggtgatcac 6180

aggcagcaac gctctgtcat cgttacaatc aacatgctac cctccgcgag atcatccgtg 6240

tttcaaaccc ggcagcttag ttgccgttct tccgaatagc atcggtaaca tgagcaaagt 6300

ctgccgcctt acaacggctc tcccgctgac gccgtcccgg actgatgggc tgcctgtatc 6360

gagtggtgat tttgtgccga gctgccggtc ggggagctgt tggctggctg gtggcaggat 6420

atattgtggt gtaaacaaat tgacgcttag acaacttaat aacacattgc ggacgttttt 6480

aatgtatgct ccaccatgtt ggcgtaaagt cttcactcct ccccctttct ctctagttag 6540

cggagacatg acaaccagtc atccgattag gtttatagtg gcattgcaag cagtcagcaa 6600

atgaataaat gaaagaggca atcttcatgg tcctcttcat cttgtctcac atgcgagttg 6660

attttagacc aacacggtaa ctcaggggat aaaatagatt tgttacaaat ttccaataag 6720

taagattcca tgaaattggt gatagtatat aatgatttta ttgcacaagc tatgcattgc 6780

agctactgat tcaacactat tcagaaaaaa aaagaacaag tgtatttctg gtaaaactgt 6840

tccattcaaa atctagtcca cgactagtcc atgatttggt cgtgtgaaaa caatggatgc 6900

actatatagt ctctagtact attctattgt actaagcact atatatagta ttataaacta 6960

cggtttatgg agtagccagc aagacaataa gttaacaaga aataaattta aagtactaaa 7020

cacaataagc caattagcat ggtgaaatga tgatttgcta tgactaatct acgactaatt 7080

gtgcgacttg ctatttggtc gagtcgtagc cctctagtcg tctgacttga ctgacgttat 7140

gactagtcta cgacttgata acagcgatcc agatgtctta agtgatgagg agaagaaaga 7200

actaccagaa agtaaacctt atatgcatag ttacatacac aggtacactt ccgaaggccc 7260

caatcaatgg aataccatat gctcttatta ggctattata tggttctggg taacaattaa 7320

atatatcatg ggtgtaccgc caatgtgaaa ttgagaactg catacacata gccacattat 7380

aaaatataaa tgcactatgc tcctgatcat ggaatgccaa ccccttatta tcaaacccaa 7440

agaagggaaa tccctttcta tctcaagcat gcacaattac ctttgtttag cataaatcta 7500

tcaaatattg caatgcaaac cttaagcaca gatgtcctcc ctcttaaata ttaatcataa 7560

tcctcagtaa atggacatac agcataaagt actttaaatt accataggtt gaattggaaa 7620

tattcttttt agtagctcac agaaaaatgg gtactaaaac taactattag taaacataaa 7680

agccccttaa tgataggagg gctctacaca agacagtcag tagcatgata accacctaca 7740

atgttgttcc tacaaataaa aatactgtag caatctctta ctaagttaaa acatactgag 7800

gttctagggt ttaaccataa gtaattagaa tatcaaaata gctcaagatt agagaaggtc 7860

ctacagaaaa acacggttat ctgcttctca aatggcctag ctacaccggg cactagcagg 7920

atcttaaaca gcactaaaat aagtatctcc cttggtcatc aaatcgaaaa gaaaatccta 7980

cagagtccac gcctttcctt ccccccacta attaacgaaa agaaacgcag agttccaatt 8040

aaggagaaag agatacgggg tacaacaaac atcgcattcg tctcgtgcta gggttttcgg 8100

gaggcgggtc tagggttgag gcaaaaaggg ggagggaatt gagcaggggg ttaccgcggt 8160

agtcgacgcc ggagttgagc ttgacgacga cggggcgccc cctgatggac ttgaggaagt 8220

cggagggcgt cttcaccgcc ccgccgccgc cgccaccgcc gccgccgccc gagccggact 8280

tctcgccgcc actgctcatc ttgcgctgcg tttgtgcggg tgcgggtgcg ggtgctagac 8340

tgctaggtct cgcggttgca tccgcatccg actttgagat cgatttttta tcgggttctg 8400

taccctccac ccgttattgg gactgaccca cctgtcatcc tcatccaatc gactgacacg 8460

cgggcccaga tcgaccccga cgtggctgtg tgtcatccta tcccaccgac atatggggcc 8520

cactgtgacg tggccccaca cgatcccatc cgagccacac atcgcctcac gctgcgtcac 8580

cgcgcgcgga caaaacaccc acacccccac actctccacc cctctctccc tctcgcccaa 8640

acccagaaac cctcgccgcc gccgccgccg ccaccaccca ccatggctac gaccgccgcg 8700

gccgcggccg ccgccctgtc cgccgccgcg acggccaaga ccggccgtaa gaaccaccag 8760

cgacaccacg tccttcccgc tcgaggccgg gtgggggcgg cggcggtcag gtgctcggcg 8820

gtgtccccgg tcaccccgcc gtccccggcg ccgccggcca cgccgctccg gccgtggggg 8880

ccggccgagc cccgcaaggg cgcggacatc ctcgtggagg cgctggagcg gtgcggcgtc 8940

agcgacgtgt tcgcctaccc gggcgccgcg tccatggaga tccaccaggc gctgacgcgc 9000

tccccggtca tcaccaacca cctcttccgc cacgagcagg gcgaggcgtt cgcggcgtcc 9060

gggtacgcgc gcgcgtccgg ccgcgtcggg gtctgcgtcg ccacctccgg ccccggggca 9120

accaacctcg tgtccgcgct cgccgacgcg ctgctcgact ccgtcccgat ggtcgccatc 9180

acgggccagg tcccccgccg catgatcggc accgacgcct tccaggagac gcccatagtc 9240

gaggtcaccc gctccatcac caagcacaat taccttgtcc ttgatgtgga ggacatcccc 9300

cgcgtcatac aggaagcctt cttcctcgcg tcctcgggcc gtcctggccc ggtgctggtc 9360

gacatcccca aggacatcca gcagcagatg gccgtgccgg tctgggacac ctcgatgaat 9420

ctaccagggt acatcgcacg cctgcccaag ccacccgcga cagaattgct tgagcaggtc 9480

ttgcgtctgg ttggcgagtc acggcgcccg attctctatg tcggtggtgg ctgctctgca 9540

tctggtgacg aattgcgctg gtttgttgag ctgactggta tcccagttac aaccactctg 9600

atgggcctcg gcaatttccc cagtgacgac ccgttgtccc tgcgcatgct tgggatgcat 9660

ggcacggtgt acgcaaatta tgccgtggat aaggctgacc tgttgcttgc gtttggtgtg 9720

cggtttgatg atcgtgtgac agggaaaatt gaggcttttg caagcagggc caagattgtg 9780

cacattgaca ttgatccagc agagattgga aagaacaagc aaccacatgt gtcaatttgc 9840

gcagatgtta agcttgcttt acagggcttg aatgctctgc tacaacagag cacaacaaag 9900

acaagttctg attttagtgc atggcacaat gagttggacc agcagaagag ggagtttcct 9960

ctggggtaca aaacttttgg tgaagagatc ccaccgcaat atgccattca ggtgctggat 10020

gagctgacga aaggtgaggc aatcatcgct actggtgttg ggcagcacca gatgtgggcg 10080

gcacaatatt acacctacaa gcggccacgg cagtggctgt cttcggctgg tctgggcgca 10140

atgggatttg ggctgcctgc tgcagctggt gcttctgtgg ctaacccagg tgtcacagtt 10200

gttgatattg atggggatgg tagcttcctc atgaacattc aggagctggc attgatccgc 10260

attgagaacc tccctgtgaa ggtgatggtg ttgaacaacc aacatttggg tatggtggtg 10320

caattggagg ataggtttta caaggcgaat agggcgcata catacttggg caacccggaa 10380

tgtgagagcg agatatatcc agattttgtg actattgcta aggggttcaa tattcctgca 10440

gtccgtgtaa caaagaagag tgaagtccgt gccgccatca agaagatgct cgagactcca 10500

gggccatact tgttggatat catcgtcccg caccaggagc atgtgctgcc tatgatccca 10560

attgggggcg cattcaagga catgatcctg gatggtgatg gcaggactgt gtattaatct 10620

agagtcctca gccatagagc tgctgctgtt ctagggttca caagtctgcc tatttgtctt 10680

ccccaatgga gctatggttg tctggtctgg tccttggtcg tgtcccgttt cattgtgtac 10740

tatttacctg taatgtgtat ccttaagtct ggtttgatgg tgtctgaaac gttttgctgt 10800

ggtagagcag catggaagaa ctataatgaa taagtgatcc ctaatcattg tgtccaaatt 10860

ttgcttctgc tatacccttt tgtgctgttt cttatgtttt gcttaaaaat ttgatctgac 10920

aaacaaattt gtc 10933

<210>5

<211>52

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>5

cgtttttaat gtatgctcca ccatgttggc gtaaagtctt cactcctccc cc 52

<210>6

<211>24

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>6

cgtagccatg gtgggtggtg gcgg 24

<210>7

<211>25

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>7

cacccaccat ggctacgacc gccgc 25

<210>8

<211>38

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>8

ggctgaggac tctagattaa tacacagtcc tgccatca 38

<210>9

<211>33

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>9

tgtattaatc tagagtcctc agccatagag ctg 33

<210>10

<211>48

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>10

tgcccgggcc tgcaggacaa atttgtttgt cagatcaaat ttttaagc 48

<210>11

<211>23

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>11

gggccatact tgttggatat cat 23

<210>12

<211>22

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>12

ttgttcatgg cgtaatgtct cc 22

<210>13

<211>19

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>13

cattgagaac ctccctgtg 19

<210>14

<211>23

<212>DNA

<213> Artificial Sequence (Artificial Sequence)

<400>14

gacaaatttg tttgtcagat caa 23

Claims

1. A rice A L S mutein characterized in that the A L S mutein has amino acid mutations at positions 95, 548 and 627 relative to the wild-type A L S protein.

2. The A L S mutein of claim 1, wherein the A L S mutein is mutated from Gly to Ala at position 95, Trp to L eu at position 548, Ser to Ile at position 627, relative to the wild-type A L S protein;

preferably, the a L S mutein has the amino acid sequence of (1) or (2) below:

(1) an amino acid sequence shown as SEQ ID NO. 1;

3. A nucleic acid encoding the a L S mutein of claim 1 or 2.

4. A biological material which is an expression cassette, vector, host cell or transgenic plant cell line comprising a nucleic acid according to claim 3.

5. Use of the a L S mutein of claim 1 or 2 or the nucleic acid of claim 3 or the biological material of claim 4 for any one of the following:

(2) the application in preparing transgenic plants;

(3) the application in the improvement of plant germplasm resources;

6. A plant transgenic screening expression cassette, which is characterized in that a plant endogenous gene is used as a screening marker, and the plant endogenous gene is an A L S mutant gene;

preferably, the A L S mutant gene is a rice A L S mutant gene;

more preferably, the protein encoded by the rice A L S mutant gene is the A L S mutant protein of claim 1 or 2.

7. The plant transgene screening expression cassette of claim 6, further comprising a promoter and a terminator for initiating and terminating transcription of the a L S mutant gene;

the promoter is a rice A L S gene promoter, a Ubi promoter, an Actin promoter, a Rubisco small subunit promoter or a Cab promoter of rice or corn;

the terminator is a rice A L S gene terminator or a Ubi terminator;

preferably, the promoter is a rice A L S gene promoter, and the terminator is a rice Ubi terminator;

more preferably, the nucleotide sequence of the expression cassette is shown in SEQ ID NO. 3.

8. A plant genetic transformation screening vector comprising the plant transgene screening expression cassette of claim 6 or 7;

preferably, the plant genetic transformation screening vector is a plant binary expression vector, and can enter the vector for genetic transformation by cloning other expression cassettes;

the other expression cassette is an expression cassette other than the plant transgene screening expression cassette of claim 6 or 7;

more preferably, the nucleotide sequence of the plant genetic transformation screening vector is shown in SEQ ID NO. 4.

9. Use of the plant transgene selection expression cassette of claim 6 or 7 or the plant genetic transformation selection vector of claim 8 in genetic transformation of plants.

10. The application according to claim 9, wherein the application comprises: after the plant transgenic screening expression cassette or the plant genetic transformation screening vector is transferred into plant callus, a screening culture medium containing herbicide is adopted for resistance screening in a screening stage;

preferably, the screening culture medium contains 0.25-1 mu mol/L Bispyribac-sodium, 200-1000 mu g/L Mexican-P or 300-1000 mu g/L imazethapyr;

and/or, the application comprises: in the differentiation stage after the plant transgenic screening expression cassette or the plant genetic transformation screening carrier is transferred into the plant callus, a differentiation culture medium containing herbicide is adopted for differentiation culture;

preferably, the differentiation medium contains 0.05-1 mu mol/L Bispyribac-sodium, 25-1000 mu g/L Mexican-P or 25-1000 mu g/L imazethapyr;

and/or the presence of a gas in the gas,

the application comprises the following steps: in the rooting stage after the plant transgenic screening expression box or the plant genetic transformation screening vector is transferred into the plant callus, a rooting culture medium containing herbicide is adopted for rooting culture;