Pervasive and Cooperative Deadenylation of 3′UTRs by Embryonic MicroRNA Families

被引:79
|
作者
Wu, Edlyn [2 ,3 ]
Thivierge, Caroline [1 ,2 ]
Flamand, Mathieu [1 ,2 ]
Mathonnet, Geraldine [4 ]
Vashisht, Ajay A. [5 ]
Wohlschlegel, James [5 ]
Fabian, Marc R. [1 ,2 ]
Sonenberg, Nahum [1 ,2 ]
Duchaine, Thomas F. [1 ,2 ,3 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3A 1A3, Canada
[2] McGill Univ, Rosalind & Morris Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, Canada
[3] CHU Ste Justine, Div Expt Med, Montreal, PQ H3T 1C5, Canada
[4] CHU Ste Justine, Lab Cytogenet, Montreal, PQ H3T 1C5, Canada
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
基金
加拿大创新基金会;
关键词
MESSENGER-RNAS; CAENORHABDITIS-ELEGANS; GENETIC INTERFERENCE; PROTEIN-SYNTHESIS; TARGET; REVEALS; MECHANISMS; PROTEOMICS; INTERACTS; BODIES;
D O I
10.1016/j.molcel.2010.11.003
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
To understand how miRNA-mediated silencing impacts on embryonic mRNAs, we conducted a functional survey of abundant maternal and zygotic miRNA families in the C. elegans embryo. We show that the miR-35-42 and the miR-51-56 miRNA families define maternal and zygotic miRNA-induced silencing complexes (miRISCs), respectively, that share a large number of components. Using a cell-free C. elegans embryonic extract, we demonstrate that the miRISC directs the rapid deadenylation of reporter mRNAs with natural 3'UTRs. The deadenylated targets are translationally suppressed and remarkably stable. Sampling of the predicted miR-35-42 targets reveals that roughly half are deadenylated in a miRNA-dependent manner, but with each target displaying a distinct efficiency and pattern of deadenylation. Finally, we demonstrate that functional cooperation between distinct miRISCs within 3'UTRs is required to potentiate deadenylation. With this report, we reveal the extensive and direct impact of miRNA-mediated deadenylation on embryonic mRNAs.
引用
收藏
页码:558 / 570
页数:13
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