CN117051133B - SNP molecular marker for detecting brucellosis resistance of sheep, detection primer and application thereof - Google Patents
SNP molecular marker for detecting brucellosis resistance of sheep, detection primer and application thereof Download PDFInfo
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Abstract
The invention relates to the technical field of molecular marker assisted breeding, in particular to SNP molecular markers for detecting brucellosis resistance of sheep, and detection primers and application thereof. The invention provides a SNP molecular marker related to brucellosis resistance of sheep, which contains a nucleotide sequence with G/A polymorphism at 101 st position of a sequence shown as SEQ ID NO. 1. The SNP molecular marker is obviously related to the brucellosis resistance of sheep, can accurately detect the resistance of sheep to the brucellosis, is used for breeding of sheep resistant to the brucellosis and molecular marker assisted breeding, and is beneficial to improving the breeding efficiency.
Description
Technical Field
The invention relates to the technical field of molecular marker assisted breeding, in particular to SNP molecular markers for detecting brucellosis resistance of sheep, and detection primers and application thereof.
Background
Brucellosis (brucellosis) is simply called brucellosis, is a systemic infectious disease of human and animal co-occurrence caused by brucellosis, and clinical symptoms of the brucellosis include wave heat, arthritis, reproductive disorders (orchitis and epididymitis of male animals, abortion and infertility of female animals) and the like. Brucella has the characteristics of immune evasion and recessive infection, wherein the virulence and infectivity of the sheep Brucella are strongest, so that huge economic loss is caused for sheep breeding industry, and the Brucella becomes a great potential safety hazard of public health. The molecular markers related to the brucellosis resistance are mined in the sheep of the host animal, and the molecular markers are applied to auxiliary disease-resistant breeding of sheep, so that the propagation path of brucellosis can be fundamentally cut off, and the environmental pollution and the drug residue hazard caused by the abuse of antibiotics can be reduced. Therefore, the molecular marker for resisting brucellosis of the mined sheep has important significance.
Disclosure of Invention
The invention provides SNP molecular markers for detecting brucellosis resistance of sheep, and detection primers and application thereof.
According to the invention, through carrying out whole genome association analysis in sheep of different varieties, SNP molecular markers related to brucellosis resistance characters in sheep genome are found, and through sheep group verification of large sample size, obvious correlation exists between the SNP molecular markers and the brucellosis resistance characters in sheep, and the SNP molecular markers can be used for detecting the resistance of sheep to brucellosis. In order to facilitate detection, the invention also develops a primer combination for detecting the SNP molecular marker.
Based on the findings, the invention provides the following technical scheme:
in a first aspect, the present invention provides a SNP molecular marker associated with brucellosis resistance in sheep, said SNP molecular marker comprising a nucleotide sequence having G/A polymorphism at position 101 of the sequence shown in SEQ ID NO. 1.
The polymorphic site of the SNP molecular marker is positioned at 35698759 of chromosome 3 of sheep reference genome with version number of oar_v1.0 and 2017, 11 months, and the polymorphism is G/A.
The SNP molecular marker has obvious correlation with the resistance of sheep to brucellosis, can accurately identify the resistance of sheep of different varieties to brucellosis, is used for molecular marker assisted breeding and variety improvement of sheep to resist brucellosis, and improves molecular breeding efficiency.
Based on the polymorphic site 35698759 of chromosome 3 of sheep reference genome with version number of oar_v1.0 and 11 in 2017, the invention develops SNP molecular marker sequence fragments and primers for amplifying the SNP molecular marker aiming at the upstream and downstream sequences of the polymorphic site for detection. By combining the upstream and downstream sequences of the polymorphic site, the sequence shown in SEQ ID NO.1 is obtained. It will be understood by those skilled in the art that sequence fragments of different lengths can be developed as SNP molecular markers based on the above SNP locus and the sequences upstream and downstream thereof, and thus the sequence shown in SEQ ID NO.1 does not constitute a limitation on the SNP molecular marker of the present invention, as long as the sequence fragment containing the polymorphic site at 35698759 position of chromosome 3 of sheep reference genome having version number of oar_v1.0, month 11 of 2017 is within the scope of protection of the SNP molecular marker of the present invention.
In some embodiments of the invention, the nucleotide sequence of the SNP molecular marker is shown as SEQ ID NO.1, the polymorphic site is positioned at 101 st position of the sequence shown as SEQ ID NO.1, and the polymorphism is G/A.
SEQ ID NO.1：
TGTTTTGCTTTCTCTTTCCTTCCATCTTTTCTTGCCCAGGTCACCCAGCTAAGGAATGGCCAAATCAGCTGGGACTCTGCCCTTTCGCTGGAGCTGGGGARAGAAGGTCCCTAGGAGGTAGGGACCAGCCCCTCAGCCTTATCCCTCCCCTTCTCTGCCAGGTCCTGGGGAGTCCGAGAAGATCCAGCAGCTGGAAGAGCA. Wherein, R is the polymorphic site of SNP molecular marker, R=G or A.
In some embodiments of the invention, the SNP molecular markers described above are amplified from primers having sequences shown in SEQ ID NO.2-4 using sheep genome as a template.
The genotype of the polymorphic site of the SNP molecular marker is GG or AA, which corresponds to the high resistance of brucellosis, and the genotype is GA, which corresponds to the low resistance of brucellosis.
In the SNP molecular marker, compared with the 'GA' heterozygous genotype, the 'GG' homozygous genotype and the 'AA' homozygous genotype, the sheep have stronger brucellosis resistance.
In a second aspect, the present invention provides a primer combination for amplifying the above-described SNP molecular marker associated with brucellosis resistance in sheep.
Based on the location of the polymorphic site of the SNP molecular marker provided above in the genome and the sequence upstream and downstream thereof, one skilled in the art can develop various types of primers for amplifying the SNP molecular marker.
The above primer may be any primer that can be used to detect the genotype of a SNP molecular marker.
Preferably, the primer combination comprises primers with sequences shown as SEQ ID NO.2-4, wherein the primers with sequences shown as SEQ ID NO.2-3 are forward primers, and the primers with sequences shown as SEQ ID NO.4 are reverse universal primers.
SEQ ID NO.2：5’-CCTACCTCCTAGGGACCTTCTT-3’；
SEQ ID NO.3：5’-CTACCTCCTAGGGACCTTCTC-3’；
SEQ ID NO.4：5’- TCACCCAGCTAAGGAATGGCCAAAT -3’。
The primer combination can realize efficient amplification and genotyping aiming at the SNP molecular markers.
KASP, i.e. competitive allele-specific PCR, can carry out high-precision double-allele typing of SNP by a specific fluorescent probe, and has stable and accurate analysis, low cost, high efficiency and easy realization of high throughput and automation. Therefore, to achieve efficient detection, the present invention developed a KASP primer combination for detecting the above-mentioned SNP molecular markers based on the KASP technique.
Preferably, the KASP primer combination comprises a first forward primer, a second forward primer and a reverse universal primer, wherein the sequence of the first forward primer is a specific fluorescent tag sequence and a sequence shown as SEQ ID NO.2 which are connected in sequence, and the sequence of the second forward primer is a specific fluorescent tag sequence and a sequence shown as SEQ ID NO.3 which are connected in sequence; the nucleotide sequence of the reverse universal primer is shown as SEQ ID NO. 4.
The fluorescent labels of the first forward primer and the second forward primer described above are different.
In some embodiments of the invention, the primer combination comprises the forward primer set forth in SEQ ID NO.5-6 and the reverse universal primer set forth in SEQ ID NO. 4.
In a third aspect, the invention provides a kit comprising a primer combination as described above.
For ease of detection, the kit may also contain other reagents for PCR amplification including, but not limited to, DNA polymerase, PCR reaction buffers, probes, dNTPs, mg 2+ Water, etc.
The above reagents may be packaged individually or may be provided as a premix after mixing.
The kit described above may have any of the following uses:
1) Detecting or assisting in detecting the resistance of sheep to brucellosis;
2) Screening or identifying sheep with high brucellosis resistance;
3) Early prediction of brucellosis resistance of sheep;
4) Molecular marker assisted breeding of sheep with brucellosis resistance;
5) Improvement of brucellosis resistance in sheep.
In a fourth aspect, the present invention provides the use of any one of the following 1) -8) of a SNP molecular marker or a detection primer for said SNP molecular marker:
1) The method is applied to detecting or assisting in detecting the resistance of sheep to brucellosis;
2) The application in preparing a reagent for detecting or assisting in detecting the resistance of sheep to brucellosis;
3) Use in screening or identifying sheep with high resistance to brucellosis;
4) Use in the preparation of a reagent for screening or identifying sheep with high resistance to brucellosis;
5) Application in early prediction of brucellosis resistance of sheep;
6) The application of the method in preparing early prediction reagent for the brucellosis resistance of sheep;
7) Application in molecular marker assisted breeding of sheep to brucellosis resistance;
8) The application in the improvement of the brucellosis resistance strain of sheep.
The polymorphic site of the SNP molecular marker is positioned at 35698759 of chromosome 3 of sheep reference genome with version number of oar_v1.0 and 2017, 11 months, and the polymorphism is G/A.
In some embodiments of the present invention, the SNP molecular marker comprises a nucleotide sequence having G/A polymorphism at position 101 of the sequence shown as SEQ ID NO. 1.
In some embodiments of the present invention, in the above application, the nucleotide sequence of the SNP molecular marker is shown as SEQ ID NO.1, the polymorphic site is located at position 101 of the sequence shown as SEQ ID NO.1, and the polymorphism is G/A.
In some embodiments of the present invention, the detection primer of the SNP molecular marker comprises a primer with a sequence shown as SEQ ID NO.2-4, wherein the primer with a sequence shown as SEQ ID NO.2-3 is a forward primer, and the primer with a sequence shown as SEQ ID NO.4 is a reverse universal primer.
In the application, the genotype of the polymorphic site of the SNP molecular marker is GG or AA, which corresponds to the high resistance of brucellosis, and the genotype is GA, which corresponds to the low resistance of brucellosis.
In the application, sheep with genotype of GG and AA are selected as parents for breeding brucellosis resistance characters.
In a fifth aspect, the invention provides a method of detecting brucellosis resistance in a sheep, the method comprising: detecting the genotype of an SNP molecular marker related to the brucellosis resistance property of sheep in a sheep genome, wherein the polymorphic site of the SNP molecular marker is positioned at 35698759 position of chromosome 3 of a sheep reference genome with a version number of oar_v1.0 and a polymorphism of G/A in 11 months 2017.
The genotype of the polymorphic locus of the SNP molecular marker is GG or AA, which corresponds to the high resistance of brucellosis, and the genotype is GA, which corresponds to the low resistance of brucellosis.
In some embodiments of the invention, the SNP molecular marker comprises a nucleotide sequence of G/A polymorphism at position 101 of the sequence as set forth in SEQ ID NO. 1.
In some embodiments of the invention, the nucleotide sequence of the SNP molecular marker is shown as SEQ ID NO.1, the polymorphic site is positioned at 101 st position of the sequence shown as SEQ ID NO.1, and the polymorphism is G/A.
Preferably, the method comprises the steps of:
1) Extracting genome DNA of sheep to be detected;
2) Using the genome DNA of the step 1) as a template, and carrying out PCR amplification by using primers with sequences shown as SEQ ID NO. 2-4;
3) Analyzing the genotype of the SNP molecular marker in the PCR amplification product, judging the resistance of the sheep to be detected to brucellosis according to the genotype, judging the sheep to be detected to have high resistance to brucellosis if the genotype of the polymorphic site of the SNP molecular marker is GG or AA, and judging the sheep to have low resistance to brucellosis if the genotype is GA.
The beneficial effects of the invention at least comprise: the SNP molecular marker related to the brucellosis resistance character of sheep is provided, the SNP molecular marker is obviously related to the brucellosis resistance of sheep, the resistance of sheep to the brucellosis can be accurately detected, the early prediction of the brucellosis resistance character of sheep can be realized, the early prediction is not limited by the age, sex and the like of sheep, even the accurate screening can be carried out immediately after the sheep is born, the SNP molecular marker can be used for breeding of the brucellosis-resistant sheep and molecular marker assisted breeding of the brucellosis-resistant character of sheep, the breeding process of the breeding of the brucellosis-resistant sheep can be obviously promoted, the breeding efficiency is effectively improved, and the SNP molecular marker has important significance for developing and utilizing the excellent economic characteristics of the excellent variety of sheep and protecting and reasonably utilizing the seed resources.
Drawings
In order to more clearly illustrate the invention or the technical solutions of the prior art, the following description will briefly explain the drawings used in the embodiments or the description of the prior art, and it is obvious that the drawings in the following description are some embodiments of the invention, and other drawings can be obtained according to the drawings without inventive effort for a person skilled in the art.
FIG. 1 shows the genotyping results of the polymorphic sites of the SNP molecular markers in example 2 according to the invention.
FIG. 2 shows the results of the population expansion verification of SNP markers in sheep populations according to example 2 of the invention, wherein p < 0.01 is represented.
Detailed Description
For the purpose of making the objects, technical solutions and advantages of the present invention more apparent, the technical solutions of the present invention will be clearly and completely described below with reference to the accompanying drawings, and it is apparent that the described embodiments are some embodiments of the present invention, not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
The invention provides an SNP molecular marker related to brucellosis resistance of sheep, wherein a polymorphic site of the SNP molecular marker is positioned at 35698759 position of chromosome 3 of sheep reference genome with version number of oar_v1.0 and 11 months in 2017, and the site has G/A base mutation and has obvious correlation with the brucellosis resistance of sheep; presumably, the site mutation may affect the ability of sheep to clear brucella; at this polymorphic site, sheep of the "GG" homozygous genotype and the "AA" homozygous genotype were more resistant to brucellosis than the "GA" heterozygous genotype. The SNP molecular marker provided by the invention has important guiding significance for distinguishing and screening sheep with brucellosis resistance characters through genotypes, and can improve the accuracy and efficiency of screening the brucellosis resistance of the sheep.
The method for detecting the genotype of the SNP molecular marker is not particularly limited, and the genotype detection method conventional in the art can be used. In a specific embodiment of the invention, the KASP method is used to detect the genotype of the SNP molecular marker in the genome of a sheep to be tested.
The SNP molecular marker related to the brucellosis resistance of sheep or the detection primer thereof can be used in combination with other SNP molecular markers related to the brucellosis resistance of sheep or the detection primers thereof for identifying the brucellosis resistance of sheep.
EXAMPLE 1 development of SNP molecular markers related to brucellosis resistance in sheep
In the embodiment, 4 sheep populations of saxifrage, dongfolishen, texol and Texol are taken as samples, and SNP molecular markers related to the anti-brucellosis property of sheep are developed by using whole genome association analysis (GWAS), and specifically are as follows:
raising sheep of the species of safock, dongfoli, texafock and Texak under the same condition, naturally infecting brucellosis, collecting sheep blood samples, and respectively detecting whether sheep is infected with the brucellosis by adopting a competitive enzyme-linked immunosorbent assay (cELSA), an indirect enzyme-linked immunosorbent assay (iELISA) and a Fluorescence Polarization Assay (FPA), wherein positive judgment threshold lines of the methods are as follows: cELISA:30, iELISA:15, FPA:20, above the threshold line, positive. And if the detection results of the three methods are positive, judging that brucella is suffered, if the detection results are negative, judging that the patient is healthy, and otherwise judging that the patient is suspicious. Finally, 25 sheep judged to have brucellosis were selected as an experimental group, 25 sheep judged to be healthy were selected as a control group, and total genome association analysis (GWAS) was performed on the 50 sheep, wherein information of the sick sheep and blood sample detection results thereof are shown in table 1, and information of the healthy sheep and blood sample detection results thereof are shown in table 2.
TABLE 1
TABLE 2
The 50 sheep blood DNA samples were subjected to whole genome re-sequencing with a sequencing platform of Huada gene T7 at a depth of 20× and a total sequencing amount of 2.6T. Sequence alignment and quality control are carried out on the sequencing data, wherein data filtering uses software fastp, alignment and mutation detection uses software GTX, and an aligned VCF file with the size of 71.08 GB is obtained. The quality control uses software PLINK, and the quality control standard is as follows: -mini 0.1-geno 0.1-maf 0.05-hwe e-5, and the effective SNP number after quality control is 24,683,444. Using software PLINK, code: the principal component analysis is performed by plink-bfile filename-pca 10-out filename-pca-chr-set 27-alloy-extra-chr. Selecting quantitative characteriELISA value), using GEMMA (Version 0.95) software, toFull genome association analysis was performed for model basis, genome assembly Oar _rambouille_v1.0 as reference genome. SNP annotation and enrichment analysis were then performed, wherein the SNP locus annotation used tool was https:// baia. Ensembl. Org/index. Html, the reference genome was Genome assembly Oar _rambouille_v1.0, the GO enrichment analysis used tool was https:// biit. Cs. Ut. Ee/gprofiler/last, the reference genome was Homo sapiens (Human), ovis aries (shaep), and the KEGG enrichment analysis used tool was: https:// david. Ncifcrf. Gov, reference genome is Homo sapiens (Human), ovis aries (Sheep).
In whole genome association analysis, top 1000 SNP-log 10 (P) has a value of 4.56-7.36, and is annotated to 100 genes, wherein-log 10 (P) 48 SNP values of 6 or more are added to 13 genes. Among the 48 SNPs, SNP molecular markers which are obviously related to the brucellosis disease resistance phenotype of sheep are selected. Finally, the SNP molecular marker related to the brucellosis resistance of sheep is obtained, the polymorphic site of the SNP molecular marker is positioned at the 35698759 rd chromosome of the 3 rd chromosome of a sheep reference genome with the version number of oar_v1.0 and the 2017 11 month, the polymorphism is G/A, the polymorphism has obvious correlation with the brucellosis resistance of sheep, the polymorphic site is cELISA value, iELISA value and FPA value of sheep individuals with 'GG' homozygous genotype and 'AA' homozygous genotype which are all obviously lower than those of 'GA' heterozygous genotype (p < 0.01), namely, compared with 'GA' heterozygous genotype, sheep with 'GG' homozygous genotype and 'AA' homozygous genotype have stronger brucellosis resistance, and 'GG' and 'AA' are dominant genotypes of brucellosis resistant sheep. The SNP molecular marker can correspond to a sequence shown as SEQ ID NO.1, wherein a polymorphic site is positioned at the 101 st position of the sequence shown as SEQ ID NO.1, and the polymorphism is G/A.
Based on the SNP molecular markers, the invention further develops KASP primers for detecting the SNP molecular markers, and the KASP primers are specifically as follows:
Primer X:
5'-gaaggtgaccaagttcatgctCCTACCTCCTAGGGACCTTCTT-3' (SEQ ID NO.5, lower case part is the specific fluorescent tag sequence FAM);
Primer Y:
5'-gaaggtcggagtcaacggattCTACCTCCTAGGGACCTTCTC-3' (SEQ ID NO.6, lower case part is the specific fluorescent tag sequence VIC);
Primer R: 5’- TCACCCAGCTAAGGAATGGCCAAAT -3’（SEQ ID NO.4）。
the polymorphic sites of the SNP molecular markers obtained above can be distinguished in the sheep population of this example by using the KASP primer as described above into three genotypes, namely the "GA" heterozygous genotype, the "GG" homozygous genotype and the "AA" homozygous genotype.
Example 2 application of SNP molecular markers related to brucellosis resistance in sheep
The SNP molecular markers developed in example 1 and related to brucellosis resistance in sheep were subjected to population expansion verification as follows:
1. collecting sheep blood sample to be tested and identifying serum antibody concentration
The jugular blood was collected from a natural brucella-infected farm from 127 safford sheep, 129 tofoprist sheep, 130 white safford sheep and 27 texel sheep that were not vaccinated. The concentration of Brucella antibody in serum is detected by adopting an indirect enzyme-linked immunosorbent assay (iELISA) method. The individual iELISA value can be used as an index for representing the disease resistance, namely, the lower the iELISA value is, the stronger the brucellosis resistance of the individual is, and the weaker the brucellosis resistance of the individual is. In the examples, the determination threshold for negative and positive in the result of the iELISA was set to 15.
2. Extracting genome DNA in sheep blood sample to be detected
And extracting genome DNA in the sheep blood sample to be detected by adopting a magnetic bead method.
3. Amplification of SNP molecular marker fragments
PCR amplification was performed using the genomic DNA extracted in the above 2 as a template and the KASP primer combinations (SEQ ID NOS.5-6 and SEQ ID NO. 4) developed in example 1, as follows:
(1) KASP amplification system:
1.6 The μl reaction system comprises: 50-100 ng/. Mu.L of genomic DNA, 0.8. Mu.L of Primer mix (preferably, primer mix ratio: 100. Mu. Mol/L of forward Primer X and Primer Y each 60. Mu.L, 100. Mu. Mol/L of universal reverse Primer R150. Mu.L, 10 mM Tris. Mu.L of HCl 230. Mu.L), 2 XMaster mix 0.4. Mu.L, and double distilled water make up 1.6. Mu.L.
The reaction system is a preferable reaction system of a Douglas Array Tape platform, and other reasonable reaction systems can achieve the same detection purpose.
Wherein the 2 XMaster mix comprises a fluorescent probe A, a fluorescent probe B, a quenching probe A and a quenching probe B, and high-fidelity Taq enzyme, dNTP and Mg 2+ Etc. The fluorescent probe A has a sequence of 5'-GAAGGTGACCAAGTTCATGCT-3', and the 5' end of the fluorescent probe A is connected with 1 fluorescent group FAM; the fluorescent probe B has a sequence of 5'-GAAGGTCGGAGTCAACGGATT-3', and the 5' end of the fluorescent probe B is connected with 1 fluorescent group VIC; the nucleotide sequence of the quenching probe A is 5'-AGCATGAACTTGGTCACCTTC-3', and the 3' -end of the quenching probe A is connected with 1 fluorescent group BHQ; the nucleotide sequence of the quenching probe B is 5'-AATCCGTTGACTCCGACCTTC-3', and the 3' -end of the quenching probe B is connected with 1 fluorescent group BHQ.
(2) PCR reaction conditions:
amplification of DNA fragment: pre-denaturation at 94 ℃ for 15 min, and setting a cycle; denaturation at 94℃for 20 s, gradient annealing at 61-55℃for 60℃ 60 s, 10 cycles were set, each cycle being reduced by 0.6 ℃.
Fluorescence signal enhancement: denaturation at 94℃for 20 s, annealing at 55℃for 60℃ 60 s, 26 cycles were set.
4. And detecting PCR amplification products by adopting a Douglas Array Tape platform to obtain genotypes of polymorphic loci of the SNP molecular markers.
The polymorphism loci genotype of the SNP molecular markers of 413 sheep were detected, and the three genotypes of "GG", "GA" and "AA" were distinguished in sheep populations as shown in Table 3 and FIG. 1. The correlation analysis of the genotype and the brucellosis resistance character shows that the iELISA values of the 'GG' and 'AA' genotype sheep individuals are obviously lower than those of the 'GA' genotype (p is less than 0.01), which shows that the brucellosis resistance of the 'GG' and 'AA' genotype sheep individuals is higher than those of the 'GA' genotype, and the 'GG' and 'AA' are dominant genotypes of brucellosis-resistant sheep.
TABLE 3 number of individuals of different genotypes at polymorphic sites of SNP molecular markers in sheep populations
Finally, it should be noted that: the above embodiments are only for illustrating the technical solution of the present invention, and are not limiting; although the invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical scheme described in the foregoing embodiments can be modified or some technical features thereof can be replaced by equivalents; such modifications and substitutions do not depart from the spirit and scope of the technical solutions of the embodiments of the present invention.
Claims (3)
- Use of any one of the following 1) -5) of detection primers for snp molecular markers:1) The application in preparing a reagent for detecting or assisting in detecting the resistance of sheep to brucellosis;2) Use in the preparation of a reagent for screening or identifying sheep with high resistance to brucellosis;3) The application of the method in preparing early prediction reagent for the brucellosis resistance of sheep;4) Application in molecular marker assisted breeding of sheep to brucellosis resistance;5) The application in the improvement of the brucellosis resistance of sheep;the polymorphic site of the SNP molecular marker is positioned at 35698759 of chromosome 3 of sheep reference genome with version number of oar_v1.0 and 2017, 11 months, and the polymorphism is G/A;the genotype of the polymorphic locus of the SNP molecular marker is GG or AA, which corresponds to the high resistance of brucellosis, and the genotype is GA, which corresponds to the low resistance of brucellosis.
- 2. The use according to claim 1, wherein the detection primer of the SNP molecular marker comprises a primer with a sequence shown as SEQ ID NO.2-4, wherein the primer with a sequence shown as SEQ ID NO.2-3 is a forward primer and the primer with a sequence shown as SEQ ID NO.4 is a reverse universal primer.
- 3. The use according to claim 1, wherein the SNP molecular marker has a nucleotide sequence shown as SEQ ID NO.1, the polymorphic site is located at position 101 of the sequence shown as SEQ ID NO.1, and the polymorphism is G/A.
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