Distinct Mechanisms for MicroRNA Strand Selection by Drosophila Argonautes

被引:238
作者
Okamura, Katsutomo [1 ]
Liu, Na [1 ]
Lai, Eric C. [1 ]
机构
[1] Sloan Kettering Inst, Dept Dev Biol, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
SMALL INTERFERING RNAS; SOMATIC-CELLS; ENDOGENOUS SIRNAS; PASSENGER-STRAND; MOUSE OOCYTES; PATHWAYS; CLEAVAGE; RISC; COMPLEXES; ROLES;
D O I
10.1016/j.molcel.2009.09.027
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 Drosophila, miRNA strands are predominantly sorted into AGO1 to regulate seed-matched target transcripts, while their partner miRNA(star) strands are thought to be mostly degraded. Here, we report that Drosophila Argonautes exhibit different strand preferences for miRNA duplexes, and that in particular, many miRNA(star) species accumulate in the RNAi effectorAG02. AGO2-loaded miRNA(star) species require canonical RNAi factors for their accumulation, are efficiently 3' modified, and are preferentially active on extensively matched target transcripts. Differential miRNA/miRNA(star) sorting profiles are correlated with specific central mismatches. In vitro assays revealed an active role for Watson-Crick base-pairing at positions 9 and 10 in promoting strand selection by AGO2, with little reciprocal effect on strand selection by AGO1. We conclude that miRNA strand selection and sorting are actually linked processes that stem from distinct loading preferences of AGO proteins and that independent sorting of duplex strands is a general feature of Drosophila microRNA genes.
引用
收藏
页码:431 / 444
页数:14
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