基于ESTSSR标记分析猕猴桃种质遗传的关系.docVIP

基于ESTSSR标记分析猕猴桃种质遗传的关系 　　摘 要: 利用开发的11对EST-SSR引物分析了33份猕猴桃种质资源的遗传多样性及其遗传关系。结果表明，11对EST-SSR引物在所有供试材料中均可扩增出清晰条带，其中有8对引物呈现多态性，多态性扩增率为72.7%，对33份种质材料的区分率达100 %。8对多态性引物共检测到61个等位基因，每对引物可检测到的等位基因数为2-17，平均为7.6个。利用NTSYS-pc软件，以不加权成对算术平均法（UPGMA）对扩增结果进行聚类，谱系图显示，33份种质材料之间的相似系数在0.60～0.97，表明猕猴桃种质之间遗传关系相对来说不是很远。在相似系数0.73的水平上可将供试猕猴桃材料分为7个类群，其结果与传统的形态分类大体一致。从分子角度揭示了猕猴桃种质资源的遗传多态性及其遗传关系。可为猕猴桃种质改良提供理论依据。EST-SSR是非常有效和可靠的分子标记，可为猕猴桃分子育种及遗传连锁图构建奠定基础。 　　关键词: 猕猴桃； EST-SSR； 种质资源； 遗传分析 　　中图分类号：Ｓ６６3．4 文献标志码：Ａ 文章编号：１００９－９９８０（２０12）０2－0212－０5 　　 　　Genetic relationships from Kiwifruit germplasms based on EST-SSR markers 　　XU Xiao-biao，LIAO Jiao，HUANG Chun-hui，GU Qing-qing，QU Xue-yan，LIU Shan-jun，CHEN Jin-yin 　　（College of Agronomy，Jiangxi Agricultural University，Nanchang, Jiangxi 330045 China） 　　Abstract: Eleven pairs of EST-SSR markers developed and designed by our lab were used to amplify the genomic DNA isolated from 33 kiwifruit genotypes (Actinidia spp.) in order to analyze their genetic diversity and relationship. The results showed that the clear DNA fragments were amplified for all materials tested by using 11 pairs of EST-SSR primers, and 8 of them showed polymorphic, accounting for 72.7%, the identification rates of 33 germplasms were up to 100%. Totally, 61 alleles were detected by 8 polymorphic pairs of EST-SSR primers, and 2 to 17 (mean 7.6) by each polymorphic primer set. Then Cluster analysis results by NTSYS-pc software based on Unweighted pair-group method arithmetic average (UPGMA) showed that the Dice similarity coefficients of 33 germplasms in kiwifruit ranged from 0.60 to 0.97, which suggested that their genetic relationships were relatively near. Thirty three accessions could be divided into seven groups according to the Dice similarity coefficient 0.73, which was consistent with the traditional classification to a certain degree. The research could reflect the kiwifruit genetic variation on molecular level by EST-SSR markers and provide theoretical basis for kiwifruit br