Fast-growing and high-quality grass carp snps and its application
An excellent technology for grass carp, applied in the field of DNA markers, can solve problems affecting gene translation efficiency, protein expression level differences, and gene transcription efficiency, etc., and achieve the effect of simple operation, excellent body width, and easy to be widely used
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Embodiment 1
[0053] Example 1 SNP marker
[0054] The grass carp gene sequence is as follows, one SNP site is found at the 175th base of SEQ ID NO.1, the 4139th base of SEQ ID NO.1, and the 4516th base of SEQ ID NO.1.
[0055] SNP1 has allele C or G at base 175 of SEQ ID NO.1, forming three genotypes CC, CG and GG; SNP2 has allele at base 4139 of SEQ ID NO.1 Gene G or C constitutes three genotypes CC, CG and GG; SNP3 has an allele G or A at base 4516 of SEQ ID NO.1, constituting two genotypes AG and GG.
Embodiment 2
[0056] Example 2 SNP site screening, verification associated with growth traits
[0057] 1. Sample Genomic DNA Extraction
[0058] Grass carp fin ray tissue was taken, and its genomic DNA was extracted (Guangzhou Meiji Biological Marine Animal Tissue Genomic DNA Extraction Kit), and the DNA integrity, DNA quality and concentration were detected.
[0059] 2. Primer Design and Synthesis
[0060] A gene fragment was obtained from the grass carp genome database. In order to verify the accuracy of the sequence and screen SNPs, 5 pairs of PCR primers P1-P5 (see Table 1 for the sequence) were designed using Primer Premier 5.0 software to amplify 24 populations from different geographical origins. , PCR primers commissioned by Guangzhou Aiji Biotechnology Co., Ltd. to synthesize.
[0061] Table 1 Sequencing primers for screening gene fragment SNPs sites
[0062]
[0063] 3. PCR amplification reaction system:
[0064]
[0065] PCR amplification reaction conditions: the amplific...
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