Timmons Lisa
Department of Molecular Biosciences, 1200 Sunnyside Avenue, University of Kansas, Lawrence, Kansas 66045, USA.
Bioessays. 2004 Jul;26(7):715-8. doi: 10.1002/bies.20078.
In eukaryotes, double-stranded RNAs (dsRNAs) or short, interfering dsRNAs (siRNAs) can reduce the accumulation of a sequence-related mRNA, often resulting in a loss-of-function phenotype-a process termed RNA interference (RNAi). Unfortunately, some mRNAs are resistant to the effects of dsRNA. Experiments designed to unravel RNAi mechanisms in Caenorhabditis elegans have led to the identification of two worm proteins, RRF-31,2 and, now, ERI-1,3 that can inhibit RNAi responses. Animals defective in either protein can display enhanced RNAi phenotypes for mRNAs that were previously resistant to dsRNA. Since ERI-1 is a conserved protein, development of procedures to enhance RNAi effectiveness in other systems may be possible.
在真核生物中,双链RNA(dsRNA)或短干扰双链RNA(siRNA)能够减少与某一序列相关的mRNA的积累,常常导致功能缺失表型,这一过程称为RNA干扰(RNAi)。不幸的是,一些mRNA对dsRNA的作用具有抗性。旨在揭示秀丽隐杆线虫RNAi机制的实验已鉴定出两种线虫蛋白,即RRF-3 1,2,以及现在的ERI-1 3,它们能够抑制RNAi反应。这两种蛋白中任一种有缺陷的动物,对于先前对dsRNA具有抗性的mRNA,都可表现出增强的RNAi表型。由于ERI-1是一种保守蛋白,因此有可能开发出在其他系统中增强RNAi有效性的方法。