Novel modes of protein-RNA recognition in the RNAi pathway

被引:67
作者
Lingel, A [1 ]
Sattler, M [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
D O I
10.1016/j.sbi.2005.01.010
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
Gene silencing mediated by RNA interference (RNAi) depends on short interfering RNAs (siRNAs) and micro RNAs (miRNAs). These RNAs have unique features, namely a defined size of 19-21 base pairs, and characteristic two-nucleotide single-stranded 3' overhangs and 5' monophosphate groups. These molecular features of siRNAs and miRNAs are produced by RNase III enzymes, which are a hallmark of gene silencing induced by double-stranded RNA. Recent structural studies of components of the RNAi pathway, including PAZ, Piwi and RNase III domains, as well as full-length Argonaute and viral p19 proteins, have revealed distinct and novel modes of sequence-independent recognition of the characteristic features of siRNAs and miRNAs in the RNAi pathway.
引用
收藏
页码:107 / 115
页数:9
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共 55 条
[51]   RECOMBINING THE STRUCTURES OF HIV INTEGRASE, RUVC AND RNASE-H [J].
YANG, W ;
STEITZ, TA .
STRUCTURE, 1995, 3 (02) :131-134
[52]   Recognition of small interfering RNA by a viral suppressor of RNA silencing [J].
Ye, KQ ;
Malinina, L ;
Patel, DJ .
NATURE, 2003, 426 (6968) :874-878
[53]   Structural requirements for pre-microRNA binding and nuclear export by Exportin 5 [J].
Zeng, Y ;
Cullen, BR .
NUCLEIC ACIDS RESEARCH, 2004, 32 (16) :4776-4785
[54]   Single processing center models for human dicer and bacterial RNase III [J].
Zhang, HD ;
Kolb, FA ;
Jaskiewicz, L ;
Westhof, E ;
Filipowicz, W .
CELL, 2004, 118 (01) :57-68
[55]   Human Dicer preferentially cleaves dsRNAs at their termini without a requirement for ATP [J].
Zhang, HD ;
Kolb, FA ;
Brondani, V ;
Billy, E ;
Filipowicz, W .
EMBO JOURNAL, 2002, 21 (21) :5875-5885