Method of screening pacific oyster EST micro-satellite mark
A technology of microsatellite markers and Pacific oysters, applied in DNA/RNA fragments, DNA preparation, recombinant DNA technology, etc.
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Embodiment 1
[0014] Example 1: Screening of microsatellite sites and determination of polymorphic markers. The Pacific oysters used in the experiment were all from Fujian farming populations.
[0015] 1. Source of microsatellite loci and screening of microsatellite sequences
[0016] Collect and download (in FASTA format) existing EST sequences from the NCBI (http: / / www.ncbi.nlm.nih.gov) database, use SSRhunter software to search and analyze the 3390 sequences obtained one by one, for 2-6 bases Microsatellite DNA sequences with basic repeating units and repeats greater than 5 were isolated. The ESTs containing microsatellites were clustered and analyzed using SeqMan in the software DNAstar, and the ESTs clustered in different contigs were selected to design primers.
[0017] 2. Design of microsatellite marker primers
[0018] Use primer design software Primer Premier 5.0 and Primerselect in DNAstar to design primers at the flanking sequences of microsatellite repeats; primers are requir...
Embodiment 2
[0026] Embodiment 2: application example
[0027] 1. DNA extraction from Pacific oysters
[0028]The Pacific oyster material used in this experiment was randomly extracted from 13 DNA samples, and DNA was extracted from frozen muscle tissue. Cut 100mg of muscle tissue, put it into 0.7ml extraction buffer (6M Urea (urea), 10mM Tris-HCl.125mM NaCl (sodium chloride), 1% SDS (sodium lauryl sarcosulphate), 10 mM EDTA (ethylenediaminetetraacetic acid), pH = 7.5), add proteinase K (20 mg / ml) at a final concentration of 0.1 mg / ml, and digest at 37°C overnight. The reactant was extracted three times with phenol:chloroform (1:1), and the extracted supernatant was extracted once with an equal volume of chloroform. The supernatant was precipitated with isopropanol, and then dissolved in 5001 μl×TE (10 mM Tris.HCl, 1 mM EDTA, pH=8.0). Treat the DNA sample with RNase (20 μg / ml) at 37°C for 1 hour, then use phenol / chloroform extraction solution for DNA purification, extract once with phen...
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