期刊文献+

ISSR标记鉴别云南茶树种质资源的研究 被引量:22

ISSR Markers for Discriminating Tea Germplasm Resources from Yunnan Province
下载PDF
导出
摘要 利用最少数量引物获得最大鉴定能力,这对种质资源的分子鉴别尤为重要。本研究应用ISSR标记技术对134份云南茶树资源进行了分子鉴别研究,用3种独立的方法对茶树种质资源进行了鉴别:特殊标记、特异的谱带类型和不同引物提供谱带类型组合。结果表明,UBC807等12个引物扩增的10个特异标记的存在和15个特异标记的缺失,可以为香竹箐大山茶等21份资源提供鉴别依据。引物UBC811扩增的54种谱带类型可以为海南大叶茶1等35份资源提供鉴别依据。UBC811、UBC835、ISSR2、ISSR3等4个引物带型的组合可以鉴别所有的134份茶树资源,并为这134份云南茶树资源的构建了可以相互区别的DNA指纹图谱。 It was of much importance using minimum primers to obtain the maximum identification ability. Molecular identification of 134 tea germplasm resources using inter-simple sequence repeat (ISSR) markers was conducted in this study. There were 3 independent ways to identify tea germplasms: a) unique ISSR markers: b) unique band patterns and c) a combination of the band patterns provided by different primers. The result showed that the presence of 10 unique ISSR markers and the absence of 15 unique markers obtained from 12 primers made it possible to identify 21 tea germplasms, including 'Xiangzhuqingdashancha' and so on. Using 54 unique band patterns of primer UBC811 could identify 35 tea germplasms, including 'Hainandayecha 1' and so on. All the 134 tea germplasms could be entirely identified by the band patterns combination of primer UBC811, UBC835, ISSR2 and ISSR3, which was successfully used to construct the ISSR fingerprinting for discriminating 134 tea germplasms from Yunnan Province.
出处 《茶叶科学》 CAS CSCD 北大核心 2009年第5期355-364,共10页 Journal of Tea Science
基金 国家科技基础条件平台建设计划(2005DKA21002)
关键词 茶树种质 鉴别 ISSR标记 tea germplasms, identification, ISSR
  • 相关文献

参考文献22

  • 1Zietkiewicz E, Rafalski A, Labuda D. Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification[J]. Genomics, 1994, 20: 176-183.
  • 2Reddy MP, Sarla N, Siddiq EA. Inter simple sequence repeat (ISSR) polymorphism and its application in plant breeding[J]. Euphytica, 2002, 128: 9-17.
  • 3陈亮,王平盛,山口聪.应用RAPD分子标记鉴定野生茶树种质资源研究[J].中国农业科学,2002,35(10):1186-1191. 被引量:44
  • 4陈亮,杨亚军,虞富莲.应用RAPD标记进行茶树优异种质遗传多态性、亲缘关系分析与分子鉴别[J].分子植物育种,2004,2(3):385-390. 被引量:20
  • 5Chen L, Gao QK, Chen DM, et al. The use of RAPD markers for detecting genetic diversity, relationship and molecular identification of Chinese elite tea genetic resources [Camellia sinensis (L.) O. Kuntze] preserved in tea germplasm repository[J]. Biodiversity and Conservation, 2005, 14(6): 1433-1444.
  • 6黎星辉,施兆鹏,刘春林,罗军武,沈程文,龚志华.云南大叶茶与汝城白毛茶杂交后代的RAPD亲子鉴定[J].茶叶科学,2001,21(2):99-102. 被引量:28
  • 7Zietkiewicz E, Rafalski A, Labuda D. Genome fingerprinting by simple sequence repeat (SSR)-anchored polymcrasv chain reaction amplification[J]. Genomics, 1994, 20: 176-183.
  • 8梁月荣,田中淳一,武田善行.应用RAPD分子标记分析“晚绿”品种的杂交亲本[J].茶叶科学,2000,20(1):22-26. 被引量:47
  • 9Yang W, de Oliveira A C, Godwin I, et al. Comparison of DNA marker technologies in characterizing plant genome diversity:variability in Chinese sorghums[J]. Crop Science, 1996, 36: 1669-1676.
  • 10刘本英 王平盛 周红杰 等.云南茶组植物ISSR-PCR反应体系的建立.云南农业大学学报,2006,:21-25.

二级参考文献106

共引文献337

同被引文献311

引证文献22

二级引证文献213

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