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RNAi-mediated targeting of heterochromatin by the RITS complex

Authors :
Steven P. Gygi
André Verdel
Scott A. Gerber
Songtao Jia
Tomoyasu Sugiyama
Shiv I. S. Grewal
Danesh Moazed
Department of cell biology
Harvard Medical School [Boston] (HMS)
Laboratory of Molecular Cell Biology
National Cancer Institute [Bethesda] (NCI-NIH)
National Institutes of Health [Bethesda] (NIH)-National Institutes of Health [Bethesda] (NIH)-National Institutes of Health
Taplin Biological Mass Spectrometry Facility
Verdel, Andre
Source :
Science, Science, American Association for the Advancement of Science (AAAS), 2004, 303 (5658), pp.672-6. ⟨10.1126/science.1093686⟩
Publication Year :
2004
Publisher :
HAL CCSD, 2004.

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.

Details

Language :
English
ISSN :
00368075 and 10959203
Database :
OpenAIRE
Journal :
Science, Science, American Association for the Advancement of Science (AAAS), 2004, 303 (5658), pp.672-6. ⟨10.1126/science.1093686⟩
Accession number :
edsair.doi.dedup.....7948badf25875d4bbe63fe90cd5fa32d
Full Text :
https://doi.org/10.1126/science.1093686⟩