A SNP locus, primer set and application for identifying the purity of pepper hybrids
A technology of hybrid purity and primer set, which is applied in the direction of recombinant DNA technology, biochemical equipment and methods, and microbial measurement/inspection, can solve the problems of inconvenient use, limited amplification methods, limited distribution, etc., and achieve Fast detection speed, broad application prospects, and the effect of improving the speed to market
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preparation example Construction
[0059] The preparation method of the above kit also belongs to the protection scope of the present invention, and the method includes packaging each primer in any one of the above primer sets separately.
[0060] In a fourth aspect, the present invention provides an authenticity detection method for identifying watermelon germplasm resources, the method comprising the following steps:
[0061] S1, DNA extraction: extract and obtain the genomic DNA of N strains of pepper hybrids to be tested; N is a natural number greater than 95; the larger the value of N, the higher the accuracy of identifying the purity of the pepper hybrids to be tested; If the value of N is too small, the purity detection is inaccurate.
[0062] S2. Target primer set screening:
[0063] S2-1: More than or equal to 8 strains, such as 8-12 strains (such as 8-10 strains, 10-12 strains, 8 strains, 10 strains or 12 strains, of the above-mentioned N pepper hybrids to be tested, the number of samples The genomi...
Embodiment 1
[0083] Obtaining the SNP site and its primer combination for identifying the purity of pepper hybrids
[0084] 1. Determination of 8 SNP sites
[0085] Based on the resequencing data of 30 peppers in the inventor's laboratory and the reference genome data of peppers, according to the screening conditions: MAF>0.1, deletion rate<0.1, heterozygosity<0.1, uniform distribution of chromosomes, and Pearson correlation coefficient with the genetic distance of the whole gene SNP Greater than 0.9, good PCA clustering effect, high discrimination and conservative 50bp sequences on both wings (no InDel, no SSR, no other SNP), a total of 32 high-quality SNPs were selected. Use these 32 pairs of SNP-KASP primers to obtain the genotypes of 82 capsicum hybrid varieties, and then screen the optimal combination with good SNP typing effect and at least one heterozygous site in the 82 hybrids, and finally determine the present invention. Eight SNP loci suitable for purity identification of peppe...
Embodiment 2
[0097] This example is the validity test of the SNP primer combination developed in Example 1. The 82 pepper hybrids tested were common excellent hybrids or hybrids introduced from abroad. The details are shown in Table 3:
[0098] Table 3: Basic information of 82 pepper hybrids tested
[0099]
[0100]
[0101] 1. Obtaining the genomic DNA of the hybrid capsicum species for testing:
[0102] The genomes of 82 leaves of pepper hybrids tested were extracted by cetyltrimethylammonium bromide (CTAB). DNA, the genomic DNA of the tested pepper hybrids was obtained.
[0103] The operation of the CTAB method is as follows: quickly grind the mixed leaves into powder in liquid nitrogen, put them in a 1.5ml centrifuge tube; add 800 μl of CTAB buffer preheated to 65°C for extraction, and extract in a water bath at 65°C for 30 minutes Add an equal volume of chloroform-isoamyl alcohol mixed solution, wherein the volume ratio of chloroform and isoamyl alcohol is 24:1, after mixing...
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