Grouper-growth-rate-related SNP (single-nucleotide polymorphism) marker and application thereof
A growth rate, grouper technology, applied in the determination/inspection of microorganisms, recombinant DNA technology, biochemical equipment and methods, etc., can solve the problem of molecular markers to be excavated and so on
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Embodiment 1
[0031] Example 1 Acquisition of SNP markers related to the growth rate of the grouper
[0032] 1.1 Acquisition of grouper populations
[0033] The group used was a grouper hatched on November 10, 2010 in a grouper farm in Hainan. The parents were 29 wild males and 12 wild females (caught in the South China Sea in Sanya, Hainan). On December 10, 2010, 15,000 fry were transferred to a cage for further rearing. On August 8, 2011, 198 individuals were randomly selected from the cage, and the dorsal fin rays of the fish were cut and stored in 95% ethanol at -20°C for genomic DNA extraction.
[0034] 1.2 Extraction of genomic DNA from the grouper
[0035] In this experiment, the conventional phenol-chloroform method was used to extract the genomic DNA in the fin rays of the grouper, and the specific steps were as follows:
[0036] (1) Take 0.3-0.5g of fin rays in a 1.5ml Eppendorf tube, cut it into pieces, and dry it for 20 minutes on a clean bench;
[0037] (2) After the ethano...
Embodiment 2
[0042] Example 2 Sequencing verification and application of SNP markers related to the growth rate of grouper
[0043] 2.1 Extraction of genomic DNA from the fin rays of the to-be-tested grouper
[0044] The grouper to be tested comes from the grouper population in Example 1, 180 fish are randomly selected, and the genomic DNA is extracted according to the DNA extraction method described in Example 1.
[0045] 2.2 Amplification of nucleotide fragments containing SNP sites
[0046] Using the genomic DNA of each tested grouper obtained from the aforementioned extraction as a template, use the forward primer F: 5'-GGGTGCTTGACAGAAGAAGG-3' (SEQ ID NO: 2) and the reverse primer R: 5'-GCTTCAAAGGGCTCTTAATGC- 3' (SEQ ID NO: 3), the nucleotide fragment where the SNP to be detected is located is amplified. Among them, the PCR reaction system is calculated as 25 μl: 50-100ng / μl template DNA 1 μl, 10pmol / μl primer F and R 1μl each, 10mmol / L dNTP mix 2.0μl, 5U / μl TaqDNA polymerase 0.125μl...
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