RNAi-Mediated Targeting of Heterochromatin by the RITS Complex

Author:

Verdel André123,Jia Songtao123,Gerber Scott123,Sugiyama Tomoyasu123,Gygi Steven123,Grewal Shiv I. S.123,Moazed Danesh123

Affiliation:

1. Department of Cell Biology, Harvard Medical School, Boston, MA02115, USA.

2. Laboratory of Molecular Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

3. Taplin Biological Mass Spectrometry Facility, Harvard Medical School, Boston, MA02115, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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