Author
Listed:
- Mitchell Guttman
(Broad Institute of MIT and Harvard, 7 Cambridge Center
Massachusetts Institute of Technology)
- Julie Donaghey
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Bryce W. Carey
(Massachusetts Institute of Technology
Whitehead Institute for Biomedical Research, 9 Cambridge Center)
- Manuel Garber
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Jennifer K. Grenier
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Glen Munson
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Geneva Young
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Anne Bergstrom Lucas
(Genomics Research and Development, Agilent Technologies)
- Robert Ach
(Genomics Research and Development, Agilent Technologies)
- Laurakay Bruhn
(Genomics Research and Development, Agilent Technologies)
- Xiaoping Yang
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Ido Amit
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Alexander Meissner
(Broad Institute of MIT and Harvard, 7 Cambridge Center
Stem Cell and Regenerative Biology, Harvard University)
- Aviv Regev
(Broad Institute of MIT and Harvard, 7 Cambridge Center
Massachusetts Institute of Technology)
- John L. Rinn
(Broad Institute of MIT and Harvard, 7 Cambridge Center
Stem Cell and Regenerative Biology, Harvard University)
- David E. Root
(Broad Institute of MIT and Harvard, 7 Cambridge Center)
- Eric S. Lander
(Broad Institute of MIT and Harvard, 7 Cambridge Center
Massachusetts Institute of Technology
Harvard Medical School)
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.
Suggested Citation
Mitchell Guttman & Julie Donaghey & Bryce W. Carey & Manuel Garber & Jennifer K. Grenier & Glen Munson & Geneva Young & Anne Bergstrom Lucas & Robert Ach & Laurakay Bruhn & Xiaoping Yang & Ido Amit & , 2011.
"lincRNAs act in the circuitry controlling pluripotency and differentiation,"
Nature, Nature, vol. 477(7364), pages 295-300, September.
Handle:
RePEc:nat:nature:v:477:y:2011:i:7364:d:10.1038_nature10398
DOI: 10.1038/nature10398
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Citations
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Cited by:
- Feng Zhi & Qiang Wang & Lian Xue & Naiyuan Shao & Rong Wang & Danni Deng & Suinuan Wang & Xiwei Xia & Yilin Yang, 2015.
"The Use of Three Long Non-Coding RNAs as Potential Prognostic Indicators of Astrocytoma,"
PLOS ONE, Public Library of Science, vol. 10(8), pages 1-14, August.
- Christian Much & Erika L. Lasda & Isabela T. Pereira & Tenaya K. Vallery & Daniel Ramirez & Jordan P. Lewandowski & Robin D. Dowell & Michael J. Smallegan & John L. Rinn, 2024.
"The temporal dynamics of lncRNA Firre-mediated epigenetic and transcriptional regulation,"
Nature Communications, Nature, vol. 15(1), pages 1-13, December.
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