Singh Brajesh K, Thomas Nadine
Macaulay Institute, Craigiebuckler, Aberdeen, UK.
Nat Protoc. 2006;1(5):2428-33. doi: 10.1038/nprot.2006.392.
A novel method called "multiplex-terminal restriction fragment length polymorphism (M-TRFLP)" has been recently developed which can be used for simultaneous analysis of the community composition of two or more microbial taxa (up to four). This method can also be used for microbial diagnostic purposes. For M-TRFLP analysis, primers specific to different target genes are used for multiplex-PCR, with one primer for each target being labeled with a unique fluorescent dye at its 5' end. Restriction digestion of the amplified products followed by fragment size analysis on a DNA sequencer produces profiles for targeted genes, which can be distinguished from each other by the color of the terminal fragments imparted by the unique fluorescent dye used for primer labeling. In contrast to current protocols, M-TRFLP allows multiple communities or multiple targets (genes) data to be obtained in just one reaction and therefore saves time, cost and labor. This protocol can be completed in 5-8 h.
最近开发了一种名为“多重末端限制性片段长度多态性(M-TRFLP)”的新方法,可用于同时分析两个或更多微生物分类群(最多四个)的群落组成。该方法也可用于微生物诊断目的。对于M-TRFLP分析,将针对不同靶基因的引物用于多重PCR,每个靶标的一个引物在其5'末端用独特的荧光染料标记。对扩增产物进行限制性消化,然后在DNA测序仪上进行片段大小分析,从而产生靶向基因的图谱,这些图谱可通过用于引物标记的独特荧光染料赋予的末端片段颜色相互区分。与当前方案相比,M-TRFLP只需一次反应就能获得多个群落或多个靶标(基因)的数据,因此节省了时间、成本和劳动力。该方案可在5-8小时内完成。