A SNP locus, primer set and application for identifying the purity of tomato hybrids
A hybrid hybrid purity and primer set technology, applied in recombinant DNA technology, biochemical equipment and methods, and microbial determination/inspection, can solve problems such as low detection accuracy, false negatives, and few sites, and achieve detection. The effect is stable and accurate, the application prospect is broad, and the effect of improving the speed to market
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preparation example Construction
[0055] 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.
[0056] In a fourth aspect, the present invention provides an authenticity detection method for identifying tomato varieties, the method comprising the following steps:
[0057] S1, DNA extraction: extract and obtain the genomic DNA of N strains of tomato 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 tomato hybrids to be tested; If the value of N is too small, the purity detection is inaccurate.
[0058] S2. Target primer set screening:
[0059] S2-1: 8 or more, for example, 8-12 strains (such as 8-10 strains, 10-12 strains, 8 strains, 10 strains or 12 strains, among the above-mentioned N strains of tomato hybrids to be tested, the number of samples The genomic DNA that is conveni...
Embodiment 1
[0080] Acquisition of SNP Sites and Primer Combinations Used to Identify the Purity of Tomato Hybrids
[0081] 1. Determination of 8 SNP sites
[0082] Based on 96 tomato resequencing data in the inventor's laboratory and tomato reference genome data, 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 genome 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.
[0083] Use these 32 pairs of SNP-KASP primers to obtain the genotypes of 163 tomato hybrid varieties, and then screen the optimal combination with good SNP typing effect and at least one heterozygous site in the 163 hybrids, and finally determine that the present invention is suitable for Eight SNP loci for purity identification of...
Embodiment 2
[0095] This example is the validity test of the SNP primer combination developed in Example 1. The 163 tested tomato hybrids were common good hybrids or hybrids introduced from abroad. The details are shown in Table 3:
[0096] Table 3: Basic information of 163 tested tomato hybrids
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[0098]
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[0100] 1. Obtaining the genomic DNA of the tested tomato hybrids:
[0101] The genomes of 163 leaves of the tested tomato hybrids were extracted by the cetyltrimethylammonium bromide (CTAB) method (30 seeds of each hybrid were taken to grow true leaves, and an equal amount of leaves were picked and mixed) DNA, the genomic DNA of the tested tomato hybrids was obtained.
[0102] 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 chl...
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