Wheeler David, Darby Brian J, Todd Timothy C, Herman Michael A
Ecological Genomics Institute, Kansas State University, Manhattan, KS 66506. ; Division of Biology, Kansas State University, Manhattan, KS 66506. ; Present address: Department of Biology, University of Rochester, Rochester, NY 14627.
J Nematol. 2012 Mar;44(1):92-101.
Phenotypic analysis of defects caused by RNA mediated interference (RNAi) in Caenorhabditis elegans has proven to be a powerful tool for determining gene function. In this study we investigated the effectiveness of RNAi in four non-model grassland soil nematodes, Oscheius sp FVV-2., Rhabditis sp, Mesorhabditis sp., and Acrobeloides sp. In contrast to reference experiments performed using C. elegans and Caenorhabditis briggsae, feeding bacteria expressing dsRNA and injecting dsRNA into the gonad did not produce the expected RNAi knockdown phenotypes in any of the grassland nematodes. Quantitative reverse-transcribed PCR (qRT-PCR) assays did not detect a statistically significant reduction in the mRNA levels of endogenous genes targeted by RNAi in Oscheius sp., and Mesorhabditis sp. From these studies we conclude that due to low effectiveness and inconsistent reproducibility, RNAi knockdown phenotypes in non-Caenorhabditis nematodes should be interpreted cautiously.
在秀丽隐杆线虫中,由RNA介导的干扰(RNAi)引起的缺陷的表型分析已被证明是确定基因功能的有力工具。在本研究中,我们调查了RNAi在四种非模式草地土壤线虫中的有效性,即Oscheius sp FVV-2、小杆线虫属、中杆线虫属和尖尾线虫属。与使用秀丽隐杆线虫和布里格氏秀丽线虫进行的对照实验不同,喂食表达dsRNA的细菌以及将dsRNA注射到性腺中,在任何一种草地线虫中都未产生预期的RNAi敲低表型。定量逆转录PCR(qRT-PCR)分析未检测到Oscheius sp.和中杆线虫属中RNAi靶向的内源性基因的mRNA水平有统计学上的显著降低。从这些研究中我们得出结论,由于效率低下和重复性不一致,非秀丽隐杆线虫中的RNAi敲低表型应谨慎解释。