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机构地区:[1]甘肃行政学院,兰州730010 [2]甘肃农业大学农学院,兰州730070 [3]中国热带农业科学院热带生物技术研究所,海口571101
出 处:《植物研究》2009年第5期628-632,共5页Bulletin of Botanical Research
摘 要:利用SSR标记对22份荔枝材料进行了亲缘关系分析,从32对引物中筛选出22对多态性引物用于荔枝SSR扩增,共扩增到52条带,其中多态性条带49条,多态性百分率为94.23%。多态性条带经POPGENE32软件统计分析表明,22个位点的平均有效等位基因频率(Ne)、平均基因杂合度(H)、平均Shannon遗传多样性指数(Hi′)分别为1.364 3、0.296 0、0.417 0。通过NTSYS聚类结果显示,在相似系数为0.51处,供试材料被聚为两大类,第一类包括13份材料,又可分为两个亚类,第二类包括9份材料。22 Litchi germplasm were used as materials for analyzing their genome polymorphism by SSR markers. 22 primers selected from 32 primers were used for SSR amplification. A total of 52 bands were generated, of which 49 bands were polymorphic bands. The percentage of polymorphic band (PPB) was 94.23%. According to the analysis results of POPGENE32 software, the average effective number of alleles( Ne), the Nei's average gene diversity (H) and the average of Shannon' s genetic diversity ( H'i ) index was 1. 364 3, 0.2960 and 0.4170, respectively. The UPGAM dendrogram gotten by NTNSYS cluster analysis implied that 22 Litchi germplasm resources could be divided into 2 groups on the basis of genetic distance 0.51. The fist group included 13 cultivars. The second group included 9 cuhivars.
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