• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

基于SSR标记分析108份金豆种质资源遗传多样性

SSR-based Analysis on Genetic Diversity of 108 Fortunella hindsi Germplasms

  • 摘要:
    目的 评估金豆(Fortunella hindsii var.chintou)种质资源遗传多样性,为其育种亲本组合的合理配置提供科学依据,进而提高育种效率。
    方法 以108份金豆种质为材料,调查13个农艺性状,并利用10对简单序列重复(simple sequence repeat, SSR)引物进行遗传多样性分析。通过计算变异系数、多态信息含量(polymorphism information content, PIC)、遗传分化指数(genetic differentiation index, Fst)等参数,结合聚类分析和分子方差分析(analysis of molecular variance, AMOVA),解析其遗传变异特征。
    结果 表型分析显示,金豆农艺性状变异系数10.51%~50.79%,表现出丰富的表型多样性。SSR标记分析共检测到41个等位基因,平均等位基因数4.1,PIC平均值为0.459(B18位点最高,达0.729),香农指数(shannon's information index, I)平均为0.945,观测杂合度(observed heterozygosity, Ho)平均为0.324,期望杂合度(expected heterozygosity, He)平均为0.515,表明群体具有丰富的遗传多样性,但存在一定近交现象。聚类分析将种质划分为5个亚群,但未呈现地理分布相关性;AMOVA显示遗传变异主要来源于个体内(53%),其次为个体间(31%)。亚群间遗传分化从中等至高度分化(Fst=0.071~0.226),其中亚群Ⅰ与其他亚群的分化达到高度分化水平(Fst>0.18)。
    结论 金豆种质资源具有较高的遗传多样性,SSR标记分析可为其种质保护与育种利用提供科学依据。

     

    Abstract:
    Objective Genetic diversity of Fortunella hindsii germplasms was analyzed to facilitate resource utilization and breeding.
    Methods A collection of 108 F. hindsii germplasms was organized based on 13 agronomic traits and 10 pairs of SSR molecular markers. The characteristic genetic variations of the collection were analyzed according to the calculated variation coefficient, polymorphism information content (PIC), genetic differentiation index (Fst), and other parameters combined with the analysis of molecular variance (AMOVA) and clustering.
    Results The phenotypic differentiation of F. hindsii was rich with the variation coefficients ranging 10.51%–50.79%. There were 41 alleles detected in the SSR markers, averaging 4.1 alleles per locus. On average, the population showing a PIC of 0.459 (locus B18 being the highest at 0.729), a Shannon's information index (I) of 0.945, an observed heterozygosity (Ho) of 0.324, and an expected heterozygosity (He) of 0.515 was genetically rich in diversity despite some degrees of inbreeding. It was clustered into 5 subpopulations without apparent correlation with the geographical distribution. The genetic variations revealed by AMOVA mainly originated within an individual germplasm at 53% and among individuals at 31%. The genetic differentiations among the subpopulations ranked from moderate to high with Fst = 0.071–0.226. Among the subpopulations, GroupⅠtopped the rest with an Fst>0.18.
    Conclusion The 108 F. hindsii germplasms demonstrated with high genetic diversity. The SSR markers applied for the analysis satisfactorily rendered the information needed for further studies on the resource conservation and breeding program.

     

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