48份鲜食葡萄种质遗传多样性的SSR分析OA
SSR Analysis on Genetic Diversity of 48 Table Grape Germplasm
[目的]探明 48份鲜食葡萄种质的遗传多样性水平和亲缘关系,为葡萄种质鉴定和遗传多样性保护及种质创新提供参考.[方法]以烟台地区 48份鲜食葡萄种质为研究对象,运用SSR技术分析遗传多样性并进行遗传结构聚类分析,构建相应的DNA指纹图谱及分子身份证.[结果]在 48份供试鲜食葡萄种质中,筛选出 9对SSR引物(A1~A4、B1~B3、C1~C2),多态性较好、条带清晰,Shannon's信息指数为2.37,Nei's基因多样性指数为 0.86,多态性信息含量为 0.85,表明 48份鲜食葡萄种质存在明显遗传差异且遗传多样性丰富.对SSR扩增条带进行分析并编码,成功构建 48份鲜食葡萄种质的指纹图谱和分子身份证.聚类结果表明,皇家秋天与其余鲜食葡萄种质亲缘关系明显较远.当遗传距离为 0.05时,其余 47份种质可分为两大类,其中,第一大类细分为 2类(遗传距离为 0.08);第二大类细分为 11类(遗传距离为 0.10),且可再向下细分 3级(遗传距离分别为 0.26、0.20、0.30),聚类结果与以农艺形态特征和成熟季节类别聚类大致相符.[结论]在 48份供试鲜食葡萄种质中,筛选的 9对引物多态性好,基于SSR技术对鲜食葡萄种质的区分率达100%,并成功构建48份鲜食葡萄种质的SSR分子指纹图谱和分子身份证.
[Objective]The genetic diversity level and genetic relationship of 48 table grape germplasm were explored to provide a reference for identification of grape germplasm,conservation of genetic diversity and innovation of grape germplasm resources.[Method]The genetic diversity and genetic structure of 48 table grape germplasms in Yantai region were analyzed by SSR and clustering technology respectively to establish their corresponding DNA finger-print chromatograms and molecular identity cards.[Result]The Shannon's information index,Nei's gene diversity index and polymorphism information content of 9 pairs of SSR primers(A1—A4,B1—B3,C1—C2)with good polymorphism and clear bands selected from 48 table grape germplasm were 2.37,0.86 and 0.85 respectively,which indicated that there were significant genetic differences and abundant genetic diversity among 48 table grape germplasm.The DNA finger-print chromatograms and molecular identity cards of 48 table grape germplasm were successfully constructed.The clustering results showed that Autumn Royal had a significantly distant genetic relationship with the other table grape germplasm.When the genetic distance was 0.05,the other 47 grape germplasm could be divided into two major groups.The groupⅠcould be further divided into 2 subgroups(genetic distance was 0.08),and the group Ⅱ could be further divided into 11 subgroups(genetic distance was 0.10),with three levels of 0.26,0.20,and 0.30 genetic distance.The clustering results were roughly consistent with the classification clustering based on agronomic morphological characteristics and maturity season.[Conclusion]9 pairs of primers with good polymorphism are successfully screened from 48 table grape germplasm.The distinction rate of table grape germplasm reaches 100%based on SSR technology and the SSR molecular fingerprint chromatogram and molecular identification cards of 48 table grape germplasm are successfully constructed.
宋超然;曹朝;李俊鹏;陈晓峰
中国农业大学 烟台研究院,山东 烟台 264670中国农业大学 烟台研究院,山东 烟台 264670中国农业大学 烟台研究院,山东 烟台 264670中国农业大学 烟台研究院,山东 烟台 264670
农业科技
SSR引物多态性鲜食葡萄分子身份证聚类分析指纹图谱
SSRprimerpolymorphismtable grapemolecular identity cardclustering analysisfingerprint chromatogram
《贵州农业科学》 2026 (2)
1-12,12
国家重点研发计划项目"主要瓜类蔬菜重要品质关键基因挖掘和功能鉴定"(2023YFE0206900)烟台市校地融合发展项目"绿色高效设施农业工程技术创新中心"(2023XDRHXMPT12)中国农业大学本科生科研训练计划(URP)项目"STR分子标记分析烟台地区鲜食葡萄种质资源遗传多样性"(U2024005)
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