国家自然科学基金(31070298、30870180);浙江省重大科技专项(2008C12081);杭州市属高校重点实验室科技创新项目(20080432T06);浙江省大学生科技创新活动计划项目(2010R421003);生物科学国家特色专业本科生科技创新项目;浙江省科技创新团队基金
为了揭示建兰(Cymbidium ensifolium)品种的遗传多样性和亲缘关系,为建兰种质资源的有效利用和开发提供依据,本文采用SRAP(sequence-related amplified polymorphism)分子标记技术对来自四川、台湾、广东的47个建兰品种的遗传多样性进行分析,应用NYSTS软件对SRAP-PCR结果进行聚类分析。结果:从88对引物中筛选获得12对特异性强、稳定性好的引物进行SRAP分析,共扩增出188条带纹,其中147条为多态性位点,平均每组引物扩增出12条多态性带。聚类分析表明,47个品种可以分为四个类群:第Ⅰ群由来自四川的3个品种组成,在Ⅱ群的23个品种中有18个来自四川、3个来自广东、2个来自台湾,第Ⅲ群的12个品种中有11个品种源于台湾,1个源于四川,在第Ⅳ群中仅有1个来自四川,其他品种均来自台湾。结果表明,由于人工驯化,造成了建兰品种遗传背景的混乱,而SRAP分子标记技术能有效地分析建兰品种的遗传多样性和亲缘关系。
In order to reveal the genetic diversity and relationships of Cymbidium ensifolium varieties and provide evidence for utilization and exploitation of germplasm resources of C. ensifolium, sequence-related amplified polymorphism (SRAP) was used to analyze the genetic relationship among the 47 varieties, which derived from Sichuan, Taiwan, and Guangdong. The software NTSYS was applied to analyze the results of SRAP-PCR. A total of 188 DNA bands was amplified using 12 specific and stable primers selected from 88 primers, 147 of which was polymorphic. The average number of polymorphic DNA bands amplified by each primer was 12. Clustering analysis revealed that these varieties were divided into four groups. Group I consisted of 3 varieties from Sichuan. In group II, 18 varieties came from Sichuan, 3 varieties from Guangdong Province, and the remaining 2 varieties from Taiwan. In 12 varieties of group III, eleven varieties came from Taiwan, and only one originated from Sichuan. In the last group, 9 varieties were included, 8 of which came from Sichuan and 1 variety originated from Taiwan. These result indicate study the genetic diversity and relationship of C. ensifolium effectively.
白坚,胡旭,周淑婷,等.47个建兰品种的SRAP遗传多样性分析[J].植物遗传资源学报,2012,13(3):376-380.
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