Distinct catalytic and non-catalytic roles of ARGONAUTE4 in RNA-directed DNA methylation

被引:327
作者
Qi, Yijun
He, Xingyue
Wang, Xiu-Jie
Kohany, Oleksiy
Jurka, Jerzy
Hannon, Gregory J.
机构
[1] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[2] Cold Spring Harbor Lab, Howard Hughes Med Inst, Cold Spring Harbor, NY 11724 USA
[3] SUNY Stony Brook, Genet Program, Stony Brook, NY 11794 USA
[4] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Plant Genom, Beijing 100101, Peoples R China
[5] Genet Informat Res Inst, Mountain View, CA 94043 USA
基金
欧盟地平线“2020”; 美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1038/nature05198
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA methylation has important functions in stable, transcriptional gene silencing, immobilization of transposable elements and genome organization(1). In Arabidopsis, DNA methylation can be induced by double-stranded RNA through the RNA interference (RNAi) pathway, a response known as RNA-directed DNA methylation(2). This requires a specialized set of RNAi components, including ARGONAUTE4 (AGO4)(3-6). Here we show that AGO4 binds to small RNAs including small interfering RNAs (siRNAs) originating from transposable and repetitive elements, and cleaves target RNA transcripts. Single mutations in the Asp-Asp-His catalytic motif of AGO4 do not affect siRNA-binding activity but abolish its catalytic potential. siRNA accumulation and non-CpG DNA methylation at some loci require the catalytic activity of AGO4, whereas others are less dependent on this activity. Our results are consistent with a model in which AGO4 can function at target loci through two distinct and separable mechanisms. First, AGO4 can recruit components that signal DNA methylation in a manner independent of its catalytic activity. Second, AGO4 catalytic activity can be crucial for the generation of secondary siRNAs that reinforce its repressive effects.
引用
收藏
页码:1008 / 1012
页数:5
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