Cargando…

Brg1 modulates enhancer activation in mesoderm lineage commitment

The interplay between different levels of gene regulation in modulating developmental transcriptional programs, such as histone modifications and chromatin remodeling, is not well understood. Here, we show that the chromatin remodeling factor Brg1 is required for enhancer activation in mesoderm indu...

Descripción completa

Detalles Bibliográficos
Autores principales: Alexander, Jeffrey M., Hota, Swetansu K., He, Daniel, Thomas, Sean, Ho, Lena, Pennacchio, Len A., Bruneau, Benoit G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392595/
https://www.ncbi.nlm.nih.gov/pubmed/25813539
http://dx.doi.org/10.1242/dev.109496
_version_ 1782366015736250368
author Alexander, Jeffrey M.
Hota, Swetansu K.
He, Daniel
Thomas, Sean
Ho, Lena
Pennacchio, Len A.
Bruneau, Benoit G.
author_facet Alexander, Jeffrey M.
Hota, Swetansu K.
He, Daniel
Thomas, Sean
Ho, Lena
Pennacchio, Len A.
Bruneau, Benoit G.
author_sort Alexander, Jeffrey M.
collection PubMed
description The interplay between different levels of gene regulation in modulating developmental transcriptional programs, such as histone modifications and chromatin remodeling, is not well understood. Here, we show that the chromatin remodeling factor Brg1 is required for enhancer activation in mesoderm induction. In an embryonic stem cell-based directed differentiation assay, the absence of Brg1 results in a failure of cardiomyocyte differentiation and broad deregulation of lineage-specific gene expression during mesoderm induction. We find that Brg1 co-localizes with H3K27ac at distal enhancers and is required for robust H3K27 acetylation at distal enhancers that are activated during mesoderm induction. Brg1 is also required to maintain Polycomb-mediated repression of non-mesodermal developmental regulators, suggesting cooperativity between Brg1 and Polycomb complexes. Thus, Brg1 is essential for modulating active and repressive chromatin states during mesoderm lineage commitment, in particular the activation of developmentally important enhancers. These findings demonstrate interplay between chromatin remodeling complexes and histone modifications that, together, ensure robust and broad gene regulation during crucial lineage commitment decisions.
format Online
Article
Text
id pubmed-4392595
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher The Company of Biologists
record_format MEDLINE/PubMed
spelling pubmed-43925952015-05-04 Brg1 modulates enhancer activation in mesoderm lineage commitment Alexander, Jeffrey M. Hota, Swetansu K. He, Daniel Thomas, Sean Ho, Lena Pennacchio, Len A. Bruneau, Benoit G. Development Stem Cells and Regeneration The interplay between different levels of gene regulation in modulating developmental transcriptional programs, such as histone modifications and chromatin remodeling, is not well understood. Here, we show that the chromatin remodeling factor Brg1 is required for enhancer activation in mesoderm induction. In an embryonic stem cell-based directed differentiation assay, the absence of Brg1 results in a failure of cardiomyocyte differentiation and broad deregulation of lineage-specific gene expression during mesoderm induction. We find that Brg1 co-localizes with H3K27ac at distal enhancers and is required for robust H3K27 acetylation at distal enhancers that are activated during mesoderm induction. Brg1 is also required to maintain Polycomb-mediated repression of non-mesodermal developmental regulators, suggesting cooperativity between Brg1 and Polycomb complexes. Thus, Brg1 is essential for modulating active and repressive chromatin states during mesoderm lineage commitment, in particular the activation of developmentally important enhancers. These findings demonstrate interplay between chromatin remodeling complexes and histone modifications that, together, ensure robust and broad gene regulation during crucial lineage commitment decisions. The Company of Biologists 2015-04-15 /pmc/articles/PMC4392595/ /pubmed/25813539 http://dx.doi.org/10.1242/dev.109496 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Stem Cells and Regeneration
Alexander, Jeffrey M.
Hota, Swetansu K.
He, Daniel
Thomas, Sean
Ho, Lena
Pennacchio, Len A.
Bruneau, Benoit G.
Brg1 modulates enhancer activation in mesoderm lineage commitment
title Brg1 modulates enhancer activation in mesoderm lineage commitment
title_full Brg1 modulates enhancer activation in mesoderm lineage commitment
title_fullStr Brg1 modulates enhancer activation in mesoderm lineage commitment
title_full_unstemmed Brg1 modulates enhancer activation in mesoderm lineage commitment
title_short Brg1 modulates enhancer activation in mesoderm lineage commitment
title_sort brg1 modulates enhancer activation in mesoderm lineage commitment
topic Stem Cells and Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392595/
https://www.ncbi.nlm.nih.gov/pubmed/25813539
http://dx.doi.org/10.1242/dev.109496
work_keys_str_mv AT alexanderjeffreym brg1modulatesenhanceractivationinmesodermlineagecommitment
AT hotaswetansuk brg1modulatesenhanceractivationinmesodermlineagecommitment
AT hedaniel brg1modulatesenhanceractivationinmesodermlineagecommitment
AT thomassean brg1modulatesenhanceractivationinmesodermlineagecommitment
AT holena brg1modulatesenhanceractivationinmesodermlineagecommitment
AT pennacchiolena brg1modulatesenhanceractivationinmesodermlineagecommitment
AT bruneaubenoitg brg1modulatesenhanceractivationinmesodermlineagecommitment