SNP locus of crassostrea gigas AHR gene
A long oyster, site technology, applied in the field of genetic breeding, can solve the problems of slow growth, long oyster germplasm degradation, increased mortality, etc., to achieve fast growth and reduce blindness
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Embodiment 1
[0017] Example 1: Acquisition of markers associated with rapid growth of the long oyster
[0018] 1. On the basis of the complete sequencing of the long oyster genome, the genes related to growth—bHLH family were obtained through GWAS association analysis technology. The bHLH family of oyster oyster was classified, including 89 genes from groups A to F. On this basis, 5 candidate genes were selected for SNP screening by resequencing, and a wild population of 417 individuals was selected. The obtained 63 loci were verified by gene chip method in the wild population of 288 individuals, and finally the association analysis with growth traits was carried out with biological software to obtain the Newchr17_8788640 SNP marker. In Newchr17_8788640-marked individuals, the growth rate of AA genotype individuals was significantly higher than that of CA genotype and CC genotype individuals.
[0019] 2. Association analysis of different genotypes and growth traits of SNP loci in Oyster o...
Embodiment 2
[0026] Example 2: Application of SNP markers in screening fast-growing long oyster parents
[0027] A kit for evaluating and screening the SNP markers of fast-growing long oyster parents was made to detect the SNP site Newchr17_8788640 of the AHR gene.
[0028] The kit contains reagents for specific amplification primers and specific extension primers required to detect SNP sites, wherein the specific amplification primer sequences for site Newchr17_8788640 are SEQ ID NO: 2 and SEQ ID NO: 3. The kit also includes common reagents required by corresponding techniques such as (10×PCR (containing Mg2+) buffer, dNTP (10mM), double distilled water, enzymes, etc. In addition, there may be standard products and controls such as determined genes).
[0029] The amplification reaction system includes: 1.0 μL of cDNA, 2.5 μL of 10×PCR (containing Mg2+) buffer, 2.0 μL of dNTP with a concentration of 10 mM, 1.0 μL of an upstream primer with a concentration of 10 μM, 1.0 μL of a downstream p...
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