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云南丹参种质资源的遗传多样性及亲缘关系的SSR分析

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为探讨云南丹参种质资源间的遗传关系,本研究采用简单重复序列(simple sequence repeats,SSR)分子标记对4种鼠尾草属植物共269份材料进行遗传多样性和亲缘关系的分析。结果表明,4种鼠尾草属植物共269份材料的平均Shannon指数(I)为0。368,平均期望杂合度(uHe)为0。236,等位基因数(Na)为1。757,有效等位基因数(Ne)为1。365。云南丹参群体的He(0。280)高于双子叶植物平均水平(He=0。191),表现较高的遗传多样性,丹参群体的He为0。151低于0。191,说明丹参群体遗传多样性较差。云南丹参与丹参共145份材料的遗传分化40%存在于种群间,60%存在于种群内,由此说明种群间的遗传变异小于种群内。采用计算最佳K值的方法,对269份材料进行了聚类分析,ΔK最大值为K=2,由此判断269份鼠尾草属资源可被分为两个类群,但ΔK在K=4时明显出现拐点,说明269份鼠尾草属资源之间存在交流。本研究通过对云南丹参EST-SSR分子标记的开发和遗传多样性的分析,可以对云南丹参F1代进行杂种鉴定,同时对云南丹参的遗传作图提供分子基础。
Genetic Diversity and Genetic Relationship of Salvia yunnanensis C.H.W.Wright Germplasm Resources by SSR Analysis
In order to explore the genetic relationship between Salvia yunnanensis C.H.W.Wright germplasm re-sources,simple sequence repeats(SSR)molecular markers were used to analyze the genetic diversity and genetic relationship of 269 materials from 4 species of Salvia plant.The results showed that the average of Shannon index(I)of269 materials from 4 populations was 0.368,the average expected heterozygosity(uHe)was 0.236,the average number of alleles(Na)was 1.757,the average effective number of alleles(Ne)was 1.365.The He of the Salvia yun-nanensis population was 0.280,which was higher than the average level of dicots(He=0.191),showing high genetic diversity.The He of the Salvia miltiorrhiza population(0.151)was lower than 0.191,indicating that the genetic diversity of the Salvia miltiorrhiza population was poor.40%of the genetic differentiation of 145 materials of the Salvia yunnanensis and Salvia miltiorrhiza Bage among the populations,and 60%exists within the populations,this showed that the genetic variation between populations was less than within populations.Using the method of calculating the best K value,cluster analysis was carried out on 269 materials,the maximum ΔK was K=2.Therefore,it can be judged that the 269 Salvia miltiorrhiza resources can be divided into two groups,but when ΔK is K=4,there is an obvious turning point,indicating that there is an exchange between the 269 Salvia resources.Through the development of EST-SSR molecular markers of Salvia yunnanensis and the analysis of genetic diversity,hybrid identification of F1 generation of Salvia yunnanensis can be carried out,and the molecular basis for genetic mapping of Salvia yunnanensis can be provided at the same time.

Salvia yunnanensis C.H.W.WrightSSR molecular markerGenetic diversityGenetic relationshipCluster analysis

田红彦、飞进强、邹转、徐绍忠

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云南农业大学农学与生物技术学院,昆明,650201

鼠尾草属植物 SSR分子标记 遗传多样性 亲缘关系 聚类分析

云南农业大学科研发展基金项目

KX900073000

2024

分子植物育种
海南省生物工程协会

分子植物育种

CSTPCD北大核心
影响因子:0.765
ISSN:1672-416X
年,卷(期):2024.22(14)