文章摘要
杨明禄1,2,3,陈世有1,.库尔勒香梨的EST-SSR 标记开发 及遗传多样性分析[J].广东农业科学,2015,42(18):127-131
查看全文    HTML 库尔勒香梨的EST-SSR 标记开发 及遗传多样性分析
Development of EST-SSR marker and geneticdiversity analysis of Korla Fragrant Pear
  
DOI:
中文关键词: 库尔勒香梨  EST-SSR  遗传多样性
英文关键词: Korla Fragrant Pear  EST-SSR  genetic diversity
基金项目:新疆生产建设兵团塔里木盆地生物资源保 护利用重点实验室开放课题(BRYB1205);国家自然科 学基金(31360440)
作者单位
杨明禄1,2,3,陈世有1, 1. 新疆生产建设兵团塔里木盆地生物资源保护利用重点实验室新疆 阿拉尔 843300 2. 塔里木大学植物科学学院新疆 阿拉尔 843300 3. 塔里木大学南疆农业有害生物综合治理重点实验室新疆 阿拉尔 843300 
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中文摘要:
      利用已公开的梨EST 序列(2 398 条)开发SSR 引物,分析梨EST 序列中SSR 分布及特征,针对 库尔勒香梨进行引物筛选,并分析受香梨优斑螟为害程度差异较大香梨18 株样本的遗传多样性。结果表明: EST 序列中有1 813 条无冗余序列,141 条含162 个SSR,占全部EST 的7.78%,出现频率8.94%,平均分布距 离为4.93 kb,但不同微卫星的重复类型间差异很大(9.51~79.87 kb),二核苷酸重复最为常见,占SSR 比例达 到51.85%。从设计的123 对引物中,选取41 对SSR 引物进行筛选,发现17 对引物扩增效果和多态性较好, 共检测出111 条多态性条带,等位基因Na 为5.53,有效等位基因数Ne 为3.74,Nei’s 基因多样性指数He 为 0.69,Shannon’s 多样性指数I 为1.40,受害较重的G 组香梨个体主要集中在UPGMA 聚类的0.78 分支处。
英文摘要:
      The SSR primers were developed by reference to the public 2 398 strips of EST sequence in pear, and by analyzing their distribution and characteristics of SSR markers,then the suitable primers specific to Kuerle Pear were sorted out,to clarify the genetic diversity of 18 pear trees which showed great variation in damage level by disoperation of Euzophera pyriella. The results showed that there were 1 813 strips of the non-redundant sequence in total of 2 398 EST sequence,of which 141 strips contained 162 SSR,amounting to 7.78% of the whole EST sequence. Their appearance rate was 8.94%,and the average distribution distance was 4.93 kb which showed extensively difference among microsatellite sequences(from 9.51 to 79.87 kb). The most common sequence was the dinucleotide repeat,which accounted for 51.85% of the whole. Choosing 41 pairs from the devised 123 pairs of primers to conduct primer screening,it was found that there were 111 strips of sequence with polymorphism bands,among which 17 strips showed favorable amplifying results and polymorphism. The allele Na was 5.53, and the number of valid allele gene Ne was 3.74,the H value of Nei’sgene diversity(H)was 0.69,and I value of Shannon’s information index(I)was 40. The individuals suffering serious damage were concentrated on the branch of 0.78 in the cluster of UPGMA.
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