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机构地区:[1]陕西师范大学生命科学学院,教育部药用植物资源与天然药物化学重点实验室 [2]洛阳师范学院生命科学系,洛阳471022
出 处:《植物生理与分子生物学学报》2007年第4期341-348,共8页Journal Of Plant Physiology and Molecular Biology
基 金:国家星火计划项目(No.2005EA850039)基金资助~~
摘 要:用扩增片段的长度多态性(amplified fragment length polymorphism,AFLP)标记分析研究了中国5个盾叶薯蓣居群30个个体的遗传多样性。筛选出9对AFLP引物,从中检测到14698条清晰可见的条带,其中多态性带12628条,多态性比率85.92%。Shannon信息指数(I)为0.3656±0.1721,物种水平的Nei基因多样性(H)为0.2322±0.2200。遗传变异分析表明,物种水平的遗传分化系数Gst为0.4827,说明其群体间存在一定的遗传分化,居群间的基因流Nm为0.5358,居群间遗传交换较小。聚类分析结果显示5个居群盾叶薯蓣有较为丰富的遗传变异,且与地理分布有相关性。Amplified fragment length polymorphism (AFLP) was used to study 30 individuals from 5 wild populations of Dioscorea zingiberensis (Table 1) for the first time. A total of 14 698 bands were detected with 9 pairs of AFLP primers and 12 686 of them were polymorphic (Tables 2, 3). On the average each primer combination could be used to detect 230 polymorphic bands and account for 85.92% of total genetic diversity at species level (Fig.2). Shannon's index of diversity (I)was 0.3656±0.1721, and Nei's gene diversity (H) was 0.2322±0.2200 at the species level. The result of genetic variance analysis showed the coefficient of genetic differentiation (Gst) was 0.4827 at species level, it indicated there were certain degree of genetic differentiation in five Dioscorea zingiberensis populations. The gene flow (Nm) among populations of D. zingiberensis was 0.5358. The datawere analyzed using unweighted pair group method, basing on arithmetic averages (UPGMA) bootstrap analysis. Cluster analyses were perfoaned by using NTSYSpc version 2.11F and Popgene 1.32 software (Figs.3, 4). The results showed that the genetic differentiation of 5 wild populations of D. zingiberensis was abundant, and 5 wild populations of D. zingiberensis could be clustered by the distance of the position basically. The AFLP molecular marker was used to identify the genetic differences of different populations of Dioscorea zingiberensis.
关 键 词:盾叶薯蓣 扩增片段的长度多态性标记 遗传 多样性:遗传结构
分 类 号:S567.239[农业科学—中草药栽培] Q943[农业科学—作物学]
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