RNAi-mediated targeting of heterochromatin by the RITS complex

被引:928
作者
Verdel, A
Jia, ST
Gerber, S
Sugiyama, T
Gygi, S
Grewal, SIS
Moazed, D [1 ]
机构
[1] NCI, Mol Cell Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Taplin Biol Mass Spectrometry Facil, Boston, MA 02115 USA
关键词
D O I
10.1126/science.1093686
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
RNA interference (RNAi) is a widespread silencing mechanism that acts at both the posttranscriptional and transcriptional levels. Here, we describe the purification of an RNAi effector complex termed RITS (RNA-induced initiation of transcriptional gene silencing) that is required for heterochromatin assembly in fission yeast. The RITS complex contains Ago1 ( the fission yeast Argonaute homolog), Chp1 ( a heterochromatin-associated chromodomain protein), and Tas3 ( a novel protein). In addition, the complex contains small RNAs that require the Dicer ribonuclease for their production. These small RNAs are homologous to centromeric repeats and are required for the localization of RITS to heterochromatic domains. The results suggest a mechanism for the role of the RNAi machinery and small RNAs in targeting of heterochromatin complexes and epigenetic gene silencing at specific chromosomal loci.
引用
收藏
页码:672 / 676
页数:5
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