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改良RNA提取法及樱桃PDV和PNRSV的RT-PCR检测
阮小凤1, Jelkmann Wilhelm2, 马锋旺1
1.College of Horticulture,Northwest SciTech University of Agriculture and Forestry;2.Federal Biological Research Center for Agriculture and Forestry,Institute for Plant Protection in Fruit Crops
摘要:
介绍了一种从木本植物组织中获得高质量RNA的快速、简单和高效的核酸提取方法。该方法是基于核酸的二氧化硅捕获,避免了使用苯酚、氯仿等有机溶剂。利用该方法从樱桃组织中提取的总RNA用RT-PCR技术检测PDV,PNRSV均获得成功。从感病植株的一年生枝的叶片、韧皮部及芽组织中扩增出了预期的目的片段,即172和449 bp,而健康组织中无此扩增带。该法提取的总RNA用于RT-PCR技术检测,其敏感性至少与商业出售的Qiagen RNeasy提取试剂盒相当,但简单经济。
关键词:  总RNA提取  二氧化硅  樱桃  PDV  PNRSV  RT-PCR检测
DOI:
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基金项目:农业部中德农业科技合作项目(1999/2000-17)
Modified RNA extraction from field woody plants for the routine detection of PDV and PNRSV in cherry by RT-PCR
Abstract:
An efficient and effective procedure for the extraction of high-quality RNA from woody plants without the use of phenol,organic solvents,or alcohol precipitation is described,which is based on silica capture.The method described has been successfully used for the detection of PDV and PNRSV in cherry by RT-PCR assay using DNA primers for the viral coat protein region.The expected sizes of the amplified products were 172 and 449 bp.Samples from bark,leaves and buds were used.Detection of viral RNA in samples of total plant RNA prepared using this method was found to be as sensitive as the methods previously described using the commercially available Qiagen's RNeasy extraction kit.
Key words:  total RNA extraction  silica  cherry  PDV  PNRSV  RT-PCR detection