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Structural determinants of miRNAs for RISC loading and slicer-independent unwinding
被引:197
作者:
Kawamata, Tomoko
[1
,2
]
Seitz, Herve
[3
,4
]
Tomari, Yukihide
[1
,2
,5
]
机构:
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Tokyo, Japan
[2] Univ Tokyo, Dept Med Genome Sci, Bunkyo Ku, Tokyo, Japan
[3] Univ Toulouse, UPS, Lab Biol Mol Eucaryote, Toulouse, France
[4] CNRS, Lab Biol Mol Eucaryote, Toulouse, France
[5] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama, Japan
基金:
日本科学技术振兴机构;
关键词:
RNA INTERFERENCE;
ENDOGENOUS SIRNAS;
PASSENGER-STRAND;
DISTINCT ROLES;
MESSENGER-RNAS;
GUIDE-STRAND;
ARGONAUTE;
MICRORNAS;
COMPLEXES;
CLEAVAGE;
D O I:
10.1038/nsmb.1630
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:
MicroRNAs (miRNAs) regulate expression of their target mRNAs through the RNA-induced silencing complex (RISC), which contains an Argonaute (Ago) family protein as a core component. In Drosophila melanogaster, miRNAs are generally sorted into Ago1-containing RISC (Ago1-RISC). We established a native gel system that can biochemically dissect the Ago1-RISC assembly pathway. We found that miRNA-miRNA* duplexes are loaded into Ago1 as double-stranded RNAs in an ATP-dependent fashion. In contrast, unexpectedly, unwinding of miRNA-miRNA* duplexes is a passive process that does not require ATP or slicer activity of Ago1. Central mismatches direct miRNA-miRNA* duplexes into pre-Ago1-RISC, whereas mismatches in the seed or guide strand positions 12-15 promote conversion of pre-Ago1-RISC into mature Ago1-RISC. Our findings show that unwinding of miRNAs is a precise mirror-image process of target recognition, and both processes reflect the unique geometry of RNAs in Ago proteins.
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页码:953 / U77
页数:9
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