首页 | 本学科首页   官方微博 | 高级检索  
     检索      

利用AFLP和SRAP标记分析19株毛木耳的遗传多样性
引用本文:许晓燕,余梦瑶,罗霞,江南,曾瑾,魏巍,郑林用.利用AFLP和SRAP标记分析19株毛木耳的遗传多样性[J].西南农业学报,2008,21(1):121-124.
作者姓名:许晓燕  余梦瑶  罗霞  江南  曾瑾  魏巍  郑林用
作者单位:1. 四川省中医药科学院,四川,成都,610041
2. 四川省中医药科学院,四川,成都,610041;四川大学生命科学院,四川,成都,610064
3. 四川省中医药科学院,四川,成都,610041;成都中医药大学,四川,成都,611137
4. 四川省农科院科技处,四川,成都,610066
摘    要:利用AFLP和SRAP标记对19株毛木耳进行遗传多样性分析。12对AFLP引物扩增得到624条片段,14对SRAP引物扩增得到459条片段,采用聚类分析都供试材料被分为4个群。结果表明,AFLP和SRAP标记均适合毛木耳遗传多样性分析,而SRAP标记较AFLP标记简便,更适于大规模的遗传多样性分析。

关 键 词:毛木耳  AFLP标记  SRAP标记
文章编号:1001-4829(2008)01-0121-04
收稿时间:2007-09-20
修稿时间:2007年9月20日

Molecular diversity of Auricularia polytricha revealed by AFLP and SRAP
XU Xiao-yan,YU Meng-yao,LUO Xia,JIANG Nan,ZENG Jin,WEI Wei,ZHENG Lin-yong.Molecular diversity of Auricularia polytricha revealed by AFLP and SRAP[J].Southwest China Journal of Agricultural Sciences,2008,21(1):121-124.
Authors:XU Xiao-yan  YU Meng-yao  LUO Xia  JIANG Nan  ZENG Jin  WEI Wei  ZHENG Lin-yong
Abstract:Due to unsatisfying attempts to fingerprint A. polytricha, two different molecular maker systems, AFLP and SRAP, were established and tested to quantify molecular diversity among 19 strains of this fungus. A total of 624 and 459 polymorphic bands were detected by 12 AFLP primers and 14 SRAP primer combinations, respectively. By parsimony method, a phylogenetic tree was constructed based on each analysis. And the two trees showed that 19 A. polytricha strains were distributed into four groups, respectively. These results demonstrated that both methods were suitable for the discriminating among strains of A. polytricha, and the novel SRAP markers are more efficient and preferable. The result also indicated that the high level of genetic diversity of A. polytricha and their relationship between each others. These finds would be benefit to future research in A. polytricha, especially in breeding and medicine development. It also gave a useful method for other fungi fingertyping.
Keywords:Auricularia polytricha  AFLP  SRAP
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号