AGO1 homeostasis entails coexpression of MIR168 and AGO1 and preferential stabilization of miR168 by AGO1

被引:286
|
作者
Vaucheret, H [1 ]
Mallory, AC
Bartel, DP
机构
[1] INRA, Biol Cellulaire Lab, Inst Jean Pierre Bourgin, F-78026 Versailles, France
[2] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[3] Howard Hughes Med Inst, Cambridge, MA 02142 USA
[4] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1016/j.molcel.2006.03.011
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
Arabidopsis ARGONAUTE1 (AGO1) encodes the RNA slicer enzyme of the microRNA (miRNA) pathway and is regulated by miR168-programmed, AGO1-catalyzed mRNA cleavage. Here, we describe two additional regulatory processes required for AGO1 homeostasis: transcriptional coregulation of MIR168 and AGO1 genes, and posttranscriptional stabilization of miR168 by AGO1. Disrupting any of these regulatory processes by using mutations or transgenes disturbs a proper functioning of the miRNA pathway. In contrast, minor perturbation leads to fine-tuned posttranscriptional adjustment of miR168 and AGO1 levels, thereby maintaining a proper balance of other miRNAs, which, together with AGO1, control the mRNA levels of miRNA targets. We suggest that miR168 stabilization occurs at the level of silencing-complex assembly and that modulating the efficiency of assembling miRNA-programmed silencing complexes will also be important in other contexts.
引用
收藏
页码:129 / 136
页数:8
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