Chromatin signature of embryonic pluripotency is established during genome activation

available in PMC 2011 April 8.

Bibliographic Details
Main Authors: Vastenhouw, Nadine L., Zhang, Yong, Woods, Ian G., Imam, Farhad, Regev, Aviv, Liu, X. Shirley, Rinn, John L., Schier, Alexander F.
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Language:en_US
Published: Nature Publishing Group 2012
Online Access:http://hdl.handle.net/1721.1/74520
https://orcid.org/0000-0001-8567-2049
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author Vastenhouw, Nadine L.
Zhang, Yong
Woods, Ian G.
Imam, Farhad
Regev, Aviv
Liu, X. Shirley
Rinn, John L.
Schier, Alexander F.
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Vastenhouw, Nadine L.
Zhang, Yong
Woods, Ian G.
Imam, Farhad
Regev, Aviv
Liu, X. Shirley
Rinn, John L.
Schier, Alexander F.
author_sort Vastenhouw, Nadine L.
collection MIT
description available in PMC 2011 April 8.
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spelling mit-1721.1/745202022-10-01T10:22:58Z Chromatin signature of embryonic pluripotency is established during genome activation Vastenhouw, Nadine L. Zhang, Yong Woods, Ian G. Imam, Farhad Regev, Aviv Liu, X. Shirley Rinn, John L. Schier, Alexander F. Massachusetts Institute of Technology. Department of Biology Regev, Aviv available in PMC 2011 April 8. After fertilization the embryonic genome is inactive until transcription is initiated during the maternal–zygotic transition. This transition coincides with the formation of pluripotent cells, which in mammals can be used to generate embryonic stem cells. To study the changes in chromatin structure that accompany pluripotency and genome activation, we mapped the genomic locations of histone H3 molecules bearing lysine trimethylation modifications before and after the maternal–zygotic transition in zebrafish. Histone H3 lysine 27 trimethylation (H3K27me3), which is repressive, and H3K4me3, which is activating, were not detected before the transition. After genome activation, more than 80% of genes were marked by H3K4me3, including many inactive developmental regulatory genes that were also marked by H3K27me3. Sequential chromatin immunoprecipitation demonstrated that the same promoter regions had both trimethylation marks. Such bivalent chromatin domains also exist in embryonic stem cells and are thought to poise genes for activation while keeping them repressed. Furthermore, we found many inactive genes that were uniquely marked by H3K4me3. Despite this activating modification, these monovalent genes were neither expressed nor stably bound by RNA polymerase II. Inspection of published data sets revealed similar monovalent domains in embryonic stem cells. Moreover, H3K4me3 marks could form in the absence of both sequence-specific transcriptional activators and stable association of RNA polymerase II, as indicated by the analysis of an inducible transgene. These results indicate that bivalent and monovalent domains might poise embryonic genes for activation and that the chromatin profile associated with pluripotency is established during the maternal–zygotic transition. National Institutes of Health (U.S.) (grant 1R01 HG004069) National Institutes of Health (U.S.) (grant 5R01 GM56211) Human Frontier Science Program (Strasbourg, France) (LT-00090/2007) European Molecular Biology Organization (fellowship) 2012-10-31T13:55:42Z 2012-10-31T13:55:42Z 2010-03 2009-08 Article http://purl.org/eprint/type/JournalArticle 0028-0836 1476-4687 http://hdl.handle.net/1721.1/74520 Vastenhouw, Nadine L. et al. “Chromatin Signature of Embryonic Pluripotency Is Established During Genome Activation.” Nature 464.7290 (2010): 922–926. Web. https://orcid.org/0000-0001-8567-2049 en_US http://dx.doi.org/10.1038/nature08866 Nature Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf Nature Publishing Group PMC
spellingShingle Vastenhouw, Nadine L.
Zhang, Yong
Woods, Ian G.
Imam, Farhad
Regev, Aviv
Liu, X. Shirley
Rinn, John L.
Schier, Alexander F.
Chromatin signature of embryonic pluripotency is established during genome activation
title Chromatin signature of embryonic pluripotency is established during genome activation
title_full Chromatin signature of embryonic pluripotency is established during genome activation
title_fullStr Chromatin signature of embryonic pluripotency is established during genome activation
title_full_unstemmed Chromatin signature of embryonic pluripotency is established during genome activation
title_short Chromatin signature of embryonic pluripotency is established during genome activation
title_sort chromatin signature of embryonic pluripotency is established during genome activation
url http://hdl.handle.net/1721.1/74520
https://orcid.org/0000-0001-8567-2049
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