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E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family
E2F transcription factors are central regulators of cell division and cell fate decisions. E2F4 often represents the predominant E2F activity in cells. E2F4 is a transcriptional repressor implicated in cell cycle arrest and whose repressive activity depends on its interaction with members of the RB...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610666/ https://www.ncbi.nlm.nih.gov/pubmed/31270324 http://dx.doi.org/10.1038/s41467-019-10901-x |
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author | Hsu, Jenny Arand, Julia Chaikovsky, Andrea Mooney, Nancie A. Demeter, Janos Brison, Caileen M. Oliverio, Romane Vogel, Hannes Rubin, Seth M. Jackson, Peter K. Sage, Julien |
author_facet | Hsu, Jenny Arand, Julia Chaikovsky, Andrea Mooney, Nancie A. Demeter, Janos Brison, Caileen M. Oliverio, Romane Vogel, Hannes Rubin, Seth M. Jackson, Peter K. Sage, Julien |
author_sort | Hsu, Jenny |
collection | PubMed |
description | E2F transcription factors are central regulators of cell division and cell fate decisions. E2F4 often represents the predominant E2F activity in cells. E2F4 is a transcriptional repressor implicated in cell cycle arrest and whose repressive activity depends on its interaction with members of the RB family. Here we show that E2F4 is important for the proliferation and the survival of mouse embryonic stem cells. In these cells, E2F4 acts in part as a transcriptional activator that promotes the expression of cell cycle genes. This role for E2F4 is independent of the RB family. Furthermore, E2F4 functionally interacts with chromatin regulators associated with gene activation and we observed decreased histone acetylation at the promoters of cell cycle genes and E2F targets upon loss of E2F4 in RB family-mutant cells. Taken together, our findings uncover a non-canonical role for E2F4 that provide insights into the biology of rapidly dividing cells. |
format | Online Article Text |
id | pubmed-6610666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66106662019-07-08 E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family Hsu, Jenny Arand, Julia Chaikovsky, Andrea Mooney, Nancie A. Demeter, Janos Brison, Caileen M. Oliverio, Romane Vogel, Hannes Rubin, Seth M. Jackson, Peter K. Sage, Julien Nat Commun Article E2F transcription factors are central regulators of cell division and cell fate decisions. E2F4 often represents the predominant E2F activity in cells. E2F4 is a transcriptional repressor implicated in cell cycle arrest and whose repressive activity depends on its interaction with members of the RB family. Here we show that E2F4 is important for the proliferation and the survival of mouse embryonic stem cells. In these cells, E2F4 acts in part as a transcriptional activator that promotes the expression of cell cycle genes. This role for E2F4 is independent of the RB family. Furthermore, E2F4 functionally interacts with chromatin regulators associated with gene activation and we observed decreased histone acetylation at the promoters of cell cycle genes and E2F targets upon loss of E2F4 in RB family-mutant cells. Taken together, our findings uncover a non-canonical role for E2F4 that provide insights into the biology of rapidly dividing cells. Nature Publishing Group UK 2019-07-03 /pmc/articles/PMC6610666/ /pubmed/31270324 http://dx.doi.org/10.1038/s41467-019-10901-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hsu, Jenny Arand, Julia Chaikovsky, Andrea Mooney, Nancie A. Demeter, Janos Brison, Caileen M. Oliverio, Romane Vogel, Hannes Rubin, Seth M. Jackson, Peter K. Sage, Julien E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title | E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title_full | E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title_fullStr | E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title_full_unstemmed | E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title_short | E2F4 regulates transcriptional activation in mouse embryonic stem cells independently of the RB family |
title_sort | e2f4 regulates transcriptional activation in mouse embryonic stem cells independently of the rb family |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610666/ https://www.ncbi.nlm.nih.gov/pubmed/31270324 http://dx.doi.org/10.1038/s41467-019-10901-x |
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