A set of core SNP markers suitable for the construction of Chinese cabbage variety nucleic acid fingerprint database and its application
A Chinese cabbage, database technology, applied in the field of core SNP markers
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Embodiment 1
[0529] Example 1, a set of SNP primers suitable for the construction of Chinese cabbage variety nucleic acid fingerprint database
[0530] 1. 96 sets of SNP core primers
[0531] The present invention designs 96 sets of SNP core primers suitable for the construction of Chinese cabbage variety nucleic acid fingerprint database based on 96 SNP sites, and each set of primers consists of 3 primer sequences. The physical positions, differential bases and nucleotide sequences of 96 sets of SNP core primers of the 96 SNP sites are shown in Table 1. 1-96 in Table 1 represent 96 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 Locus 1 is located at No. 1248141 on chromosome A01, and its base is T or C.
[0532] The physical positions of the above-mentioned 96 SNP sites are determined based on the ...
Embodiment 2
[0541] Embodiment 2, the application of the SNP primer group that is suitable for Chinese cabbage variety nucleic acid fingerprint database construction
[0542] 1. Genomic DNA extraction
[0543] Genomic DNA of 328 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:
[0544] 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 to mix well, and place in...
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