SNP (single nucleotide polymorphism) marker related to rapid growth of micropterus salmoide L. 'excellent bass No. 1' and application of SNP marker
A largemouth bass and marking technology, which is applied in the direction of microbial determination/inspection, recombinant DNA technology, biochemical equipment and methods, etc., can solve the problems of cannibalism, parental quality of largemouth bass, and large growth disparity , to achieve the effects of fast growth, reduced blindness, and stable genetics
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Embodiment 1
[0023] Example 1 Acquisition of SNP markers related to the rapid growth of largemouth bass "Youzhu No. 1"
[0024] 1. Acquisition of SNP markers
[0025] The new breeding species of largemouth bass "Youyu No. 1" is a largemouth bass obtained through 5 consecutive generations of selective breeding based on 4 breeding populations in China. Breeding species of perch. The growth rate of this new species is 17.8%-25.3% faster than that of common largemouth bass, and the deformity rate of high back and short tail is reduced from 5.2% to 1.1%. This variety was approved by the National Aquatic Original Species and Improved Breeds Approval Committee in 2010, and the approval number is GS01-004-2010. During the breeding process, we compared the production performance of the selective breeding group and the non-selective breeding group of largemouth bass. We used metal wire code marks to mark 800 breeding groups and non-selective breeding groups that were close to the time of breeding,...
Embodiment 2
[0036] Example 2 Application of the above-mentioned SNP sites in screening fast-growing largemouth bass parents
[0037] Utilize above-mentioned SNP locus to screen fast-growing largemouth bass parent, comprise the following steps:
[0038] 1) Cut fin ray samples from the parent to be tested and extract DNA;
[0039] 2) Using the extracted DNA as a template, use specific primers for primary PCR amplification to obtain primary PCR products,
[0040] 3) Use the Snapshot method to use the first-time PCR product as a template, use the extension primer to extend a base to terminate at the polymorphic site, and detect it on the sequencer. According to the color of the peak, the base type of the polypeptide site can be known to determine the target to be tested Whether the parents are homozygous.
[0041] The reaction system for the initial PCR amplification is:
[0042] dna 1μl 10×buffer 1.5μl 25mmol of MgCl 2
1.5μl dNTP 0.3μl 20P upstrea...
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