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小麦基因组的一种简易提取方法
引用本文:师丽红,杨文香,刘大群.小麦基因组的一种简易提取方法[J].中国农学通报,2010,26(19):22-26.
作者姓名:师丽红  杨文香  刘大群
作者单位:河北农业大学植物病理系分子植物病理学实验室,河北省农作物病虫害生物防治工程技术研究中心,河北保定,071001
基金项目:国家公益性行业(农业)科研专项,国家"十一五"支撑计划 
摘    要:改良发展一种快速简便、高效的小麦基因组DNA提取方法,命名为TENR提取法。以春小麦Thatcher和以Thatcher为遗传背景的近等基因系TcLr19、TcLr20、TcLr28为试验材料,采用TENR提取法提取其基因组DNA,DNA提取质量通过紫外分光光度分析法和琼脂糖凝胶电泳法并结合抗叶锈基因Lr20的STS标记、Lr19和Lr28的SCAR标记、Lr28的SSR标记进行PCR扩增检测进行评价。结果表明,TENR提取法获得的DNA质量合格,且能扩增出条带清晰正确的分子标记目的片段。该方法能够获得适用于STS、SCAR、SSR标记PCR扩增的高质量的DNA,而且加快了DNA提取速度、降低了成本、减少了污染源,为大批量提取DNA提供了技术支撑。

关 键 词:福建    福建    农业竞争力    综合评价    动态分析
收稿时间:2010/4/28 0:00:00
修稿时间:2010/5/24 0:00:00

One simple method for extracting of the wheat genome
Shi Lihong,Yang Wenxiang,Liu Daqun.One simple method for extracting of the wheat genome[J].Chinese Agricultural Science Bulletin,2010,26(19):22-26.
Authors:Shi Lihong  Yang Wenxiang  Liu Daqun
Institution:( Laboratory of Molecular Phytopathology , Department of Plant Pathology , Agricultural University of Hebei / Biological Control Centre of Plant Diseases and Pests of Hebei Province , Baoding Hebei 071001)
Abstract:One easy and efficient wheat genomic DNA extraction method had been developed and named as TENR extraction method. Spring wheat cultivar Thatcher, the near-isogenic lines TcLr19, TcLr20 and TcLr28 which taken the Thatcher as the genetic background were used as the materials and the DNA were extracted by TENR method. The quality of DNA were evaluated by UV spectrophotometric analysis, agarose gel electrophoresis method and PCR amplification using the STS marker for leaf rust resistance gene Lr20, SCAR markers for Lr19 and Lr28, SSR marker for Lr28. The results showed that high qualified DNA was obtained by TENR extraction method, clear and right bands were amplified in the test. The method could reduce the DNA extracting processing, costs, pollution to the environment, and get high quality DNA for PCR analysis. It provided base for the preparation of large number of samples for PCR-based assays.
Keywords:wheat  TENR extraction method  STS  SCAR  SSR markers PCR amplification
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