基于微卫星标记4个鲍养殖群体的遗传多样性分析

    Analysis of genetic diversity in four populations of abalone using microsatellite markers

    • 摘要:
      目的 本研究旨在系统解析鲍养殖群体的遗传多样性水平、群体遗传结构及分化特征,为鲍的遗传选育及种质资源保护提供科学依据。
      方法 本研究采用7对微卫星标记对福建省皱纹盘鲍(Haliotis discus hannai,ZPB)、绿盘鲍(皱纹盘鲍♀ × 绿鲍♂,Haliotis discus hannai ♀ × H. fulgens ♂,LPB)、绿盘鲍与皱纹盘鲍回交第一代F1绿杂鲍(ZPB ♀ × LPB ♂,LZB)和西盘鲍(皱纹盘鲍♀ × 西氏鲍♂,Haliotis discus hannai ♀ × H. gigantea ♂,XPB)四个养殖群体进行遗传多样性分析。
      结果 结果显示,7个位点的平均等位基因数(Na)为16,有效等位基因数(Ne)为2.856~11.517,观测杂合度(Ho)为0.410~0.930,期望杂合度(He)为0.653~0.918,多态信息含量(PIC)为0.611~0.907。LZB与XPB的遗传距离(Ds)最小(0.106),遗传一致度(I)最高;LPB与XPB的Ds最大(0.440),I最低。群体间的遗传分化程度(Fst)为0.000~0.069,基因流(Nm)为3.378~999.750。分子方差分析(AMOVA)结果表明,4%遗传变异来自群体间,10%来自内个体间,86%来自个体内;4个鲍养殖群体可聚为3支。
      结论 LPB、ZPB群体遗传多样性较低,LZB、XPB群体遗传多样性较高。本研究结果为鲍养殖群体遗传多样性变化趋势提供证据,也为鲍资源的科学管理与养殖业健康发展提供参考。

       

      Abstract:
      Objective The purpose of this study is to systematically analyze the genetic diversity, population genetic structure and differentiation characteristics of abalone cultured populations, thereby providing a scientific basis for genetic selection and germplasm resource conservation in abalone.
      Methods Using SSR technology, we analyzed genetic diversity in the four abalone cultured populations in Fujian Province including Haliotis discus hannai (ZPB), Haliotis discus hannai ♀ × H. fulgens ♂ (LPB), ZPB ♀ × LPB ♂ (LZB) and Haliotis discus hannai ♀ × H. gigantea ♂ (XPB).
      Results The results showed the average number of alleles (Na) was 16 across seven loci, with the effective number of alleles (Ne) ranging from 2.856 to 11.517. Observed heterozygosity (Ho) ranged from 0.410 to 0.930, while expected heterozygosity (He) was between 0.653 and 0.918, with polymorphism information content (PIC) spanning 0.611 to 0.907. The genetic distance between LZB and XPB was the smallest (0.106), and the identity (I) was the highest. The genetic distance between LPB and XPB was the largest (0.440), and the identity was the lowest. The degree of fixation statistics (Fst) among populations ranged from 0.000 to 0.069, and the number of migrants (Nm) ranged from 3.378 to 999.750. Analysis of molecular variance (AMOVA) revealed that 4% of genetic variation originated from among populations, 10% from among indiviual, and 86% from within indiviual. Four cultured abalone groups could be divided into three groups.
      Conclusion The genetic diversity of LPB and ZPB populations is low, and the genetic diversity of LZB and XPB populations is high. These resluts provide evidence for the change trend of genetic diversity of abalone culture population, and provide reference for the scientific management of abalone resources and the healthy development of aquaculture industry.

       

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