Methods for acquiring micro-satellite sequence and polymorphic micro-satellite markers of hucho taimen and polymorphic micro-satellite markers of hucho taimen
A technology of microsatellite sequence and microsatellite marker, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, and microbial determination/inspection, can solve the time-consuming and labor-intensive development of microsatellite markers, increase the risk of microsatellite sequence separation and Cost and other issues, to achieve the effect of low cost and high safety
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specific Embodiment approach 1
[0020] Specific embodiment 1: In this embodiment, the microsatellite sequence of salmon salmon is obtained according to the following steps: 1. Extraction of salmon genome DNA; 2. Enzyme digestion of salmon genome DNA and construction of microsatellite enrichment library; 3. Bacteria colony PCR amplification and positive clone detection and sequencing, that is, to obtain the microsatellite sequence of jellyfish salmon.
specific Embodiment approach 2
[0021] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that in step 2, restriction endonucleases are used to single-enzyme or double-enzyme digest the salmon genome DNA. Other steps and parameters are the same as those in Embodiment 1.
specific Embodiment approach 3
[0022] Specific implementation mode three: the difference between this implementation mode and specific implementation mode two is: the steps are divided into the following steps to realize:
[0023] a. Enzyme digestion of salmon genome DNA:
[0024]The jelly salmon genomic DNA digestion system is 20 μL, which consists of 2 μL 10× digestion buffer, 0.2 μL BSA with a concentration of 10 ng / μL, 2.5 U restriction endonucleases, 5 μL jelly salmon genomic DNA with a concentration of 100 ng / μL and The remaining amount is composed of sterilized deionized water; the enzyme digestion incubation time is 4h;
[0025] b. Connection:
[0026] The ligation system was 40 μL, which consisted of 20 μL of enzyme-digested fragments in step a, 2 μL of sticky-end double-stranded adapters, 4 μL of 10×buffer, 6 Weiss units of T4 DNA ligase and the rest of sterilized deionized water, and ligated overnight in a water bath at 4°C; The double-stranded linker was prepared according to the following ste...
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