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Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor

Maintaining quiescent cells in G0 phase is achieved in part through the multiprotein subunit complex known as DREAM, and in human cell lines the transcription factor E2F4 directs this complex to its cell cycle targets. We found that E2F4 binds a highly overlapping set of human genes among three dive...

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Autores principales: Conboy, Caitlin M., Spyrou, Christiana, Thorne, Natalie P., Wade, Elizabeth J., Barbosa-Morais, Nuno L., Wilson, Michael D., Bhattacharjee, Arindam, Young, Richard A., Tavaré, Simon, Lees, Jacqueline A., Odom, Duncan T.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2020443/
https://www.ncbi.nlm.nih.gov/pubmed/17957245
http://dx.doi.org/10.1371/journal.pone.0001061
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author Conboy, Caitlin M.
Spyrou, Christiana
Thorne, Natalie P.
Wade, Elizabeth J.
Barbosa-Morais, Nuno L.
Wilson, Michael D.
Bhattacharjee, Arindam
Young, Richard A.
Tavaré, Simon
Lees, Jacqueline A.
Odom, Duncan T.
author_facet Conboy, Caitlin M.
Spyrou, Christiana
Thorne, Natalie P.
Wade, Elizabeth J.
Barbosa-Morais, Nuno L.
Wilson, Michael D.
Bhattacharjee, Arindam
Young, Richard A.
Tavaré, Simon
Lees, Jacqueline A.
Odom, Duncan T.
author_sort Conboy, Caitlin M.
collection PubMed
description Maintaining quiescent cells in G0 phase is achieved in part through the multiprotein subunit complex known as DREAM, and in human cell lines the transcription factor E2F4 directs this complex to its cell cycle targets. We found that E2F4 binds a highly overlapping set of human genes among three diverse primary tissues and an asynchronous cell line, which suggests that tissue-specific binding partners and chromatin structure have minimal influence on E2F4 targeting. To investigate the conservation of these transcription factor binding events, we identified the mouse genes bound by E2f4 in seven primary mouse tissues and a cell line. E2f4 bound a set of mouse genes that was common among mouse tissues, but largely distinct from the genes bound in human. The evolutionarily conserved set of E2F4 bound genes is highly enriched for functionally relevant regulatory interactions important for maintaining cellular quiescence. In contrast, we found minimal mRNA expression perturbations in this core set of E2f4 bound genes in the liver, kidney, and testes of E2f4 null mice. Thus, the regulatory mechanisms maintaining quiescence are robust even to complete loss of conserved transcription factor binding events.
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spelling pubmed-20204432007-10-24 Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor Conboy, Caitlin M. Spyrou, Christiana Thorne, Natalie P. Wade, Elizabeth J. Barbosa-Morais, Nuno L. Wilson, Michael D. Bhattacharjee, Arindam Young, Richard A. Tavaré, Simon Lees, Jacqueline A. Odom, Duncan T. PLoS One Research Article Maintaining quiescent cells in G0 phase is achieved in part through the multiprotein subunit complex known as DREAM, and in human cell lines the transcription factor E2F4 directs this complex to its cell cycle targets. We found that E2F4 binds a highly overlapping set of human genes among three diverse primary tissues and an asynchronous cell line, which suggests that tissue-specific binding partners and chromatin structure have minimal influence on E2F4 targeting. To investigate the conservation of these transcription factor binding events, we identified the mouse genes bound by E2f4 in seven primary mouse tissues and a cell line. E2f4 bound a set of mouse genes that was common among mouse tissues, but largely distinct from the genes bound in human. The evolutionarily conserved set of E2F4 bound genes is highly enriched for functionally relevant regulatory interactions important for maintaining cellular quiescence. In contrast, we found minimal mRNA expression perturbations in this core set of E2f4 bound genes in the liver, kidney, and testes of E2f4 null mice. Thus, the regulatory mechanisms maintaining quiescence are robust even to complete loss of conserved transcription factor binding events. Public Library of Science 2007-10-24 /pmc/articles/PMC2020443/ /pubmed/17957245 http://dx.doi.org/10.1371/journal.pone.0001061 Text en Conboy et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Conboy, Caitlin M.
Spyrou, Christiana
Thorne, Natalie P.
Wade, Elizabeth J.
Barbosa-Morais, Nuno L.
Wilson, Michael D.
Bhattacharjee, Arindam
Young, Richard A.
Tavaré, Simon
Lees, Jacqueline A.
Odom, Duncan T.
Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title_full Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title_fullStr Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title_full_unstemmed Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title_short Cell Cycle Genes Are the Evolutionarily Conserved Targets of the E2F4 Transcription Factor
title_sort cell cycle genes are the evolutionarily conserved targets of the e2f4 transcription factor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2020443/
https://www.ncbi.nlm.nih.gov/pubmed/17957245
http://dx.doi.org/10.1371/journal.pone.0001061
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