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植物研究 ›› 2009, Vol. 29 ›› Issue (3): 346-351.doi: 10.7525/j.issn.1673-5102.2009.03.018

• 论文 • 上一篇    下一篇

党参基因组DNA提取、ISSR-PCR反应体系优化及引物筛选

安娜1;郭宏波1*;周铜水2;吴千红2   

  1. (1.西北农林科技大学生命科学学院,杨凌712100) (2.复旦大学天然药物研究中心,上海200433)
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2009-05-20 发布日期:2009-05-20
  • 通讯作者: 郭宏波
  • 基金资助:
     

DNA Isolation,Optimization of ISSR-PCR System and Primers Screening of Codonopsis pilosula(Franch.) Nannf.

AN Na;GUO Hong-Bo*;ZHOU Tong-Shui;WU Qian-Hong   

  1. (1.College of Life Science,Northwest A & F University,Yangling712100) (2.Research Center of Natural Medicine,Fudan University,Shanghai200433)
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-05-20 Published:2009-05-20
  • Contact: GUO Hong-Bo
  • Supported by:
     

摘要: 对党参基因组DNA提取方法优化、ISSR体系形成及引物筛选三方面进行探讨,为研究党参居群遗传多样性及药材DNA鉴定奠定基础。经比较改良CTAB法、改进的高盐SDS法和试剂盒三种常用DNA提取方法,发现改良CTAB法效果最佳;利用优化设计并结合有关文献优化ISSR反应体系,最优反应体系为:50 μL总反应体积中含约20 ng DNA模板,1.25 U Taq DNA聚合酶,2.25 mmol·L-1 Mg2+,200 μmol·L-1 dNTP,0.50 μmol·L-1引物。以此体系为基础进行引物筛选,在100条ISSR引物中筛选出13条扩增条带清晰、多态性较高、重复性好的引物。

关键词: 党参, DNA提取, ISSR-PCR反应体系, 引物筛选

Abstract: To assess genetic diversity and to authenticate the medicinal materials of Codonopsis pilosula(Franch.) Nannf. the present work including DNA isolation, optimization of PCR assay of inter-simple sequence repeat (ISSR) and primers screening were investigated. Among three DNA isolation methods, improved CTAB, improved SDS and isolation kit, the improved CTAB was found to be the best. Based on priority selection design and those results in reported references, the optimal ISSRPCR action was carried out in a volume of 50 μL containing 20 ng of genomic DNA, 1.25 U of Taq polymerase, 1×buffer, 200 μmol·L-1 each of dATP, dGTP, dCTP and dTTP, 0.5 μmol·L-1 of primer, and 2.25 μmol·L-1 Mg2+. According to this PCR system, thirteen of one hundred primers were chosen for their clarity, high polymorphism and repeatition.

Key words: Codonopsis pilosula, DNA isolation, optimization of ISSR-PCR system, primer screening

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