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The Xist lncRNA interacts directly with SHARP to silence transcription through HDAC3

Colleen A. McHugh, Chun-Kan Chen, Amy Chow, Christine F. Surka, Christina Tran, Patrick McDonel, Amy Pandya-Jones, Mario Blanco, Christina Burghard, Annie Moradian, Michael J. Sweredoski, Alexander A. Shishkin, Julia Su, Eric S. Lander, Sonja Hess, Kathrin Plath and Mitchell Guttman ()
Additional contact information
Colleen A. McHugh: California Institute of Technology
Chun-Kan Chen: California Institute of Technology
Amy Chow: California Institute of Technology
Christine F. Surka: California Institute of Technology
Christina Tran: California Institute of Technology
Patrick McDonel: Broad Institute of MIT and Harvard
Amy Pandya-Jones: Jonsson Comprehensive Cancer Center, Molecular Biology Institute, University of California Los Angeles
Mario Blanco: California Institute of Technology
Christina Burghard: California Institute of Technology
Annie Moradian: Proteome Exploration Laboratory, Beckman Institute, California Institute of Technology
Michael J. Sweredoski: Proteome Exploration Laboratory, Beckman Institute, California Institute of Technology
Alexander A. Shishkin: California Institute of Technology
Julia Su: California Institute of Technology
Eric S. Lander: Broad Institute of MIT and Harvard
Sonja Hess: Proteome Exploration Laboratory, Beckman Institute, California Institute of Technology
Kathrin Plath: Jonsson Comprehensive Cancer Center, Molecular Biology Institute, University of California Los Angeles
Mitchell Guttman: California Institute of Technology

Nature, 2015, vol. 521, issue 7551, 232-236

Abstract: The mechanisms by which Xist, a long non-coding RNA, silences one X chromosome in female mammals are unknown; here a mass spectrometry-based approach is developed to identify several proteins that interact directly with Xist, including the transcriptional repressor SHARP that is required for transcriptional silencing through the histone deacetylase HDAC3.

Date: 2015
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DOI: 10.1038/nature14443

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