Specific marker for male and female genetic sex of oplegnathus punctatus, identification method and kit
A porphyra, specific technology, applied in the field of specific markers and identification methods and kits for the genetic sex of porphyra male and female, can solve the problems of unstable amplification products, inconsistent amplification efficiency of target bands, confusion, etc. , to achieve rapid and accurate identification and improve the genetic breeding process of porpoise
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Embodiment 1
[0033] Example 1 Screening and verification of male and female shared and male-specific DNA markers
[0034] Discovery of hermaphrodite Y chromosome with a large insertion target DNA sequence:
[0035] The DNA sequence of the heteromorphic chromosome (neoY) of the male fish used in the present invention and the X of the female fish 1 Chromosomal DNA sequence, from the Institute of Oceanology, Chinese Academy of Sciences, Marine Fish Aquaculture and Breeding Technology Laboratory Li Jun's research team entrusted Guangzhou Kidio Biotechnology Co., Ltd. to complete the female and male porpoise using the third-generation PacBio whole-genome sequencing technology. The genome was sequenced and assembled, and the assembly results were basically consistent with the published genome information of the grouper (CNP0001488, Li et al., 2021). Using comparative genomic bioinformatics to analyze the genome sequences of the male and female porpoise visible (see figure 1 ), Porpoise female...
Embodiment 2
[0043] Example 2 Establishment and Application of Genetic Sex Determination Technology for Male and Female Porpoise
[0044] Genetic sex identification was carried out on the grouper bream from Laizhou Mingbo Aquatic Products Co., Ltd. in Laizhou, Yantai, Shandong (among them, 12 phenotypes were female and 12 phenotypes were male):
[0045] High-quality DNA extraction: use the Tiangen Marine Animal DNA Extraction Kit to extract the DNA from the fin ray of the grouper, use 0.8% agarose gel electrophoresis to identify the integrity of the genomic DNA, and use a UV spectrophotometer to measure the OD value of the DNA supernatant. Adjust the DNA concentration to 60ng / µL and freeze it at -20°C for later use.
[0046] PCR reaction system and Touch down PCR amplification identification: The sex-specific DNA fragment primers ChXY_F: 1 and ChXY_R: 2 were used to detect the genetic sex of the red sea bream by PCR. PCR reaction system 25µL: 10×Buffer 5.0µL, dNTP 4.0µL, rTaq enzyme (5U / µ...
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