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lincRNAs act in the circuitry controlling pluripotency and differentiation

Authors :
Guttman, Mitchell
Donaghey, Julie
Carey, Bryce W.
Garber, Manuel
Grenier, Jennifer K.
Munson, Glen
Young, Geneva
Lucas, Anne Bergstrom
Ach, Robert
Bruhn, Laurakay
Yang, Xiaoping
Amit, Ido
Meissner, Alexander
Regev, Aviv
Rinn, John L.
Root, David E.
Lander, Eric S.
Source :
Nature. September 15, 2011, Vol. 477 Issue 7364, p295, 11 p.
Publication Year :
2011

Abstract

Although thousands of large intergenic non-coding RNAs (lincRNAs) have been identified in mammals, few have been functionally characterized, leading to debate about their biological role. To address this, we performed loss-of- function studies on most lincRNAs expressed in mouse embryonic stem (ES) cells and characterized the effects on gene expression. Here we show that knockdown of lincRNAs has major consequences on gene expression patterns, comparable to knockdown of well-known ES cell regulators. Notably, lincRNAs primarily affect gene expression in trans. Knockdown of dozens of lincRNAs causes either exit from the pluripotent state or upregulation of lineage commitment programs. We integrate lincRNAs into the molecular circuitry of ES cells and show that lincRNA genes are regulated by key transcription factors and that lincRNA transcripts bind to multiple chromatin regulatory proteins to affect shared gene expression programs. Together, the results demonstrate that lincRNAs have key roles in the circuitry controlling ES cell state.<br />The mammalian genome encodes many thousands of large noncoding transcripts1 including a class of ~3,500 lincRNAs identified using a chromatin signature of actively transcribed genes2-4. These lincRNA genes have been [...]

Details

Language :
English
ISSN :
00280836
Volume :
477
Issue :
7364
Database :
Gale General OneFile
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
edsgcl.267976405
Full Text :
https://doi.org/10.1038/nature10398