Core SNP (single nucleotide polymorphism) marker system suitable for building variety nucleic acid fingerprint database of non-heading Chinese cabbage and its application
A technology of head cabbage and varieties, applied in the direction of recombinant DNA technology, microbe measurement/inspection, DNA/RNA fragments, etc.
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Embodiment 1
[0358] Example 1, a set of SNP primers suitable for the construction of non-heading Chinese cabbage variety nucleic acid fingerprint database
[0359] 1. 62 sets of SNP core primers
[0360] The present invention designs 62 sets of SNP core primers suitable for constructing the nucleic acid fingerprint database of non-heading cabbage varieties based on 62 SNP sites, and each set of primers consists of 3 primer sequences. The physical positions, differential bases and nucleotide sequences of the 62 sets of SNP core primers of the 62 SNP sites are shown in Table 1. 1-62 in Table 1 represent 62 SNP sites, the linkage group represents the chromosome number, the physical position represents the number of digits on the chromosome corresponding to the SNP site, and the difference base represents the base of the SNP site, such as SNP Site 1 is located at position 4878711 on chromosome A01, and its base is T or C.
[0361] The physical positions of the above-mentioned 62 SNP sites ar...
Embodiment 2
[0369] Embodiment 2, the application of the SNP primer group that is suitable for non-heading Chinese cabbage variety nucleic acid fingerprint database construction
[0370] 1. Genomic DNA extraction
[0371] Genomic DNA of 124 non-heading Chinese cabbage varieties to be tested in 53 provinces and cities in Table 2 were extracted respectively. The extraction method can be the conventional CTAB method or the method of rapid and high-throughput extraction of plant genomic DNA. The invention adopts conventional CTAB method to extract genome DNA. Specific steps are as follows:
[0372] First, take 4-5 seeds from each material to accelerate germination for 2-3 days, put the small buds with two green cotyledons into a 2mL centrifuge tube individually, add 1 0.4mm steel ball, write the number clearly, put it into the liquid Freeze in nitrogen for 5-10 minutes, and then crush using a tissue grinder. Add 800 μL of CTAB buffer solution preheated at 65°C to each tube, vortex quickly t...
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