Alteration of miRNA activity via context-specific modifications of Argonaute proteins

被引:33
作者
Jee, David [1 ,2 ]
Lai, Eric C. [1 ]
机构
[1] Sloan Kettering Inst, Dept Dev Biol, New York, NY 10065 USA
[2] Weill Cornell Grad Sch Med Sci, Program Biochem Cell & Mol Biol, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
Argonaute; miRNA; hydroxylation; phosphorylation; ubiquitination; PARylation; MICRORNA EXPRESSION; RNA INTERFERENCE; TRANSCRIPTIONAL REGULATION; EMBRYONIC-DEVELOPMENT; MAMMALIAN-CELLS; DICER; BIOGENESIS; PATHWAY; TARGETS; COMPLEXES;
D O I
10.1016/j.tcb.2014.04.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
miRNAs are enclosed within Argonaute (Ago) proteins, the downstream effectors of small RNA-mediated gene silencing. Because miRNAs mediate extensive networks of post-transcriptional control, cells have evolved multiple strategies to control their activity with precision. A growing theme of recent years is how post-translational modifications of Ago proteins, such as prolyl hydroxylation, phosphorylation, ubiquitination, and poly-ADP-ribosylation, alter miRNA activity at global or specific levels. In this review, we discuss recent advances in Ago modifications in mammalian cells and emphasize how such alterations modulate small RNA function to coordinate appropriate downstream cellular responses. These findings provide a framework to understand how Ago protein modifications are linked to reorganization of post-transcriptional regulatory networks, enabling dynamic responses to diverse external stimuli and changing environmental conditions.
引用
收藏
页码:546 / 553
页数:8
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