Functional anatomy of a dsRNA trigger: Differential requirement for the two trigger strands in RNA interference

被引:299
作者
Parrish, S
Fleenor, J
Xu, SQ
Mello, C
Fire, A
机构
[1] Carnegie Inst Sci, Baltimore, MD 21210 USA
[2] Johns Hopkins Univ, Biol Grad Program, Baltimore, MD 21218 USA
[3] Univ Massachusetts, Ctr Canc, Dept Cell Biol, Program Mol Med, Worcester, MA 01605 USA
关键词
D O I
10.1016/S1097-2765(00)00106-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In RNA-mediated interference (RNAi), externally provided mixtures of sense and antisense RNA trigger concerted degradation of homologous cellular RNAs. We show that RNAi requires duplex formation between the two trigger strands, that the duplex must include a region of identity between trigger and target RNAs, and that duplexes as short as 26 bp can trigger RNAi. Consistent with in vitro observations, a fraction of input dsRNA is converted in vivo to short segments of similar to 25 nt. Interference assays with modified dsRNAs indicate precise chemical requirements for both bases and backbone of the RNA trigger. Strikingly, certain modifications are well tolerated on the sense, but not the antisense, strand, indicating that the two trigger strands have distinct roles in the interference process.
引用
收藏
页码:1077 / 1087
页数:11
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