SNP marker relevant to ammonia endurance capacity of epinephelus coioides and use of SNP marker
A grouper and marking technology, which is applied in the direction of recombinant DNA technology, microbial measurement/inspection, DNA/RNA fragments, etc., can solve the problems of molecular markers to be excavated, and achieve the effect of promoting the breeding process
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Embodiment 1
[0048] Example 1: Obtainment of SNP markers related to ammonia tolerance of Epinephelus covidii.
[0049] 1.1 The acquisition of the grouper grouper.
[0050] The population used was the fertilized eggs of grouper from a grouper farm in Hainan. The parents were 15 males and 26 females (all F1 generations of wild grouper), 2kg of fertilized eggs It was transferred to Shenzhen Huada Ocean Technology Co., Ltd. Baguang base for incubation. Eight months later, 1,000 individuals with fertilized eggs of Epinephelus nigra were randomly selected for the ammonia tolerance test.
[0051] 1.2 Ammonia tolerance test of Epinephelus slantii.
[0052] The experimental fish had an average body length of 18 cm and an average weight of 78 g. The experimental water is sand-filtered seawater, the water temperature is (21±0.5)℃, the salinity is 26-28, the pH is 7.8-8.0, and the dissolved oxygen is 4.5-5.5mg / L. According to preliminary experiments, this specification of Epinephelus obliquus to ammonia ni...
Embodiment 2
[0062] Example 2: Sequencing verification and application of SNP markers related to the ammonia tolerance of Epinephelus slantii.
[0063] 2.1 Extract the genomic DNA from the fin rays of the grouper.
[0064] The grouper to be tested came from the grouper grouper in Example 1. 300 fish were selected, and the genomic DNA was extracted according to the DNA extraction method described in Example 1.
[0065] 2.2 Amplify nucleotide fragments containing SNP sites.
[0066] Using the genomic DNA of each grouper to be tested obtained by the aforementioned extraction as the template, forward primer F: 5'-CGATGTAATCCAACATTTCCTGA-3' (SEQ ID NO. 2) and reverse primer R: 5'-GATTACAGGGGAAAAACTGCAGAGC- 3'(SEQ ID NO. 3), amplify the nucleotide fragment where the SNP to be tested is located.
[0067] Among them, the PCR reaction system in 25μl is: 50-100ng / μl template DNA 1μl, 10pmol / μl primers F and R each 1μl, 10mmol / L dNTP mix 2.0μl, 5U / μl Taq DNA polymerase 0.125μl, 10×PCR The reaction buffer was...
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