天然河豚与人工河豚群体遗传差异的PCR分析。

Development & reproduction Pub Date : 2020-12-01 Epub Date: 2020-12-31 DOI:10.12717/DR.2020.24.4.327
Jong-Man Yoon
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引用次数: 2

摘要

采用聚合酶链反应(PCR)技术对天然河豚和人工河豚两种群的基因组DNA进行扩增。在两个地点发现的碎片的复杂程度差别很大。养殖群体中15 ~ 12号个体的遗传距离(GDs)为0.053,是已知最小的。寡核苷酸引物OPC-11鉴定出每个群体共有88个独特的位点,反映了自然群体。OPC-05引物鉴定出两个种群共有的44个位点。自然种群个体的平均带共享值(0.683±0.014)低于培养种群个体的平均带共享值(0.759±0.009)(p
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Genetic Differences in Natural and Cultured River Pufferfish Populations by PCR Analysis.

Genomic DNA (gDNA) extracted from two populations of natural and cultured river pufferfish (Takifugu obscurus) was amplified by polymerase chain reaction (PCR). The complexity of the fragments derived from the two locations varied dramatically. The genetic distances (GDs) between individuals numbered 15 and 12 in the cultured population was 0.053, which was the lowest acknowledged. The oligonucleotide primer OPC-11 identified 88 unique loci shared within each population reflecting the natural population. The OPC-05 primer identified 44 loci shared by the two populations. The average band-sharing (BS) values of individuals in the natural population (0.683±0.014) were lower than in those derived from the cultured population (0.759±0.009) (p<0.05). The shortest GD demonstrating a significant molecular difference was found between the cultured individuals # 15 and # 12 (GD=0.053). Individual # 02 of the natural population was most distantly related to cultured individual # 22 (GD=0.827). A cluster tree was built using the unweighted pair group method with arithmetic mean (UPGMA) Euclidean GD analysis based on a total of 578 various fragments derived from five primers in the two populations. Obvious markers identified in this study represent the genetic structure, species security, and proliferation of river pufferfish in the rivers of the Korean peninsula.

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