期刊文献+

小苍兰种质遗传多样性的ISSR分析 被引量:14

ISSR Analysis of Genetic Diversity in Freesia refracta Germplasm
在线阅读 下载PDF
导出
摘要 利用ISSR(Inter Simple Sequence Repeat)分子标记对12份小苍兰(Freesia refracta)种质进行了遗传多样性分析研究。从34条ISSR引物中筛选出了12条适宜的引物。这12条引物中每条引物可扩增出5~11条DNA片段,共扩增了96个条带,其中多态性片段62条,平均每条引物可产生5.2条多态性片段,多态性条带比率(PPB)为64.6%。经NTSYS-pc分析,12份小苍兰种质间的遗传距离(GD)的变化范围为0.123~0.907,平均为0.442。根据Nei’s相似系数建立了UPGMA聚类图,在相似系数为0.56时,可将紫色花系的小苍兰种质与其它种质分开,形成两个组。结果表明,ISSR分子标记可有效地分析小苍兰种质资源的遗传多样性和亲缘关系,为小苍兰的杂交育种和新品种保护提供理论基础。 Genetic diversity of 12 Freesia refracta accessions was detected and assessed using inter simple sequence repeat (ISSR) markers. From 34 ISSR primers, 12 primers were selected to perform ISSR-PCR. 5 -11 DNA fragments were amplified with each of the 12 primers. Total 96 DNA bands were obtained, of which 62 bands had polymorphism, and average 5.2 polymorphic bands per primer. The percentage of polymorphic bands (PPB) was 64.6%. Computed with NTSYS-pc, the genetic distance (GD) of the 12 F. refracta accessions from 0. 123 to 0. 907, and average 0. 442. According to the UPGMA dendrogram based on Nei's genetic group 1, and the others to the group 2. The results demonstrated that ISSR is a useful tool to analyze the genetic diversity and genetic relationship among F. refracta accessions, which provides a scientific basis for cross breed- ing and new varieties protection of F. refracta.
出处 《植物研究》 CAS CSCD 北大核心 2009年第3期357-361,共5页 Bulletin of Botanical Research
基金 国家自然科学基金项目(30571474) 国家自然科学基金项目(30872061)
关键词 小苍兰 遗传多样性 ISSR Freesia refracta genetic diversity ISSR
  • 相关文献

参考文献19

二级参考文献104

共引文献318

同被引文献201

引证文献14

二级引证文献103

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部