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Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells

When self-renewing pluripotent cells receive a differentiation signal, ongoing cell duplication needs to be coordinated with entry into a differentiation program. Accordingly, transcriptional activation of lineage specifier genes and cell differentiation is confined to the G(1) phase of the cell cyc...

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Autores principales: Asenjo, Helena G., Gallardo, Amador, López-Onieva, Lourdes, Tejada, Irene, Martorell-Marugán, Jordi, Carmona-Sáez, Pedro, Landeira, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056320/
https://www.ncbi.nlm.nih.gov/pubmed/32181346
http://dx.doi.org/10.1126/sciadv.aay4768
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author Asenjo, Helena G.
Gallardo, Amador
López-Onieva, Lourdes
Tejada, Irene
Martorell-Marugán, Jordi
Carmona-Sáez, Pedro
Landeira, David
author_facet Asenjo, Helena G.
Gallardo, Amador
López-Onieva, Lourdes
Tejada, Irene
Martorell-Marugán, Jordi
Carmona-Sáez, Pedro
Landeira, David
author_sort Asenjo, Helena G.
collection PubMed
description When self-renewing pluripotent cells receive a differentiation signal, ongoing cell duplication needs to be coordinated with entry into a differentiation program. Accordingly, transcriptional activation of lineage specifier genes and cell differentiation is confined to the G(1) phase of the cell cycle by unknown mechanisms. We found that Polycomb repressive complex 2 (PRC2) subunits are differentially recruited to lineage specifier gene promoters across cell cycle in mouse embryonic stem cells (mESCs). Jarid2 and the catalytic subunit Ezh2 are markedly accumulated at target promoters during S and G(2) phases, while the transcriptionally activating subunits EPOP and EloB are enriched during G(1) phase. Fluctuations in the recruitment of PRC2 subunits promote changes in RNA synthesis and RNA polymerase II binding that are compromised in Jarid2 −/− mESCs. Overall, we show that differential recruitment of PRC2 subunits across cell cycle enables the establishment of a chromatin state that facilitates the induction of cell differentiation in G(1) phase.
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spelling pubmed-70563202020-03-16 Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells Asenjo, Helena G. Gallardo, Amador López-Onieva, Lourdes Tejada, Irene Martorell-Marugán, Jordi Carmona-Sáez, Pedro Landeira, David Sci Adv Research Articles When self-renewing pluripotent cells receive a differentiation signal, ongoing cell duplication needs to be coordinated with entry into a differentiation program. Accordingly, transcriptional activation of lineage specifier genes and cell differentiation is confined to the G(1) phase of the cell cycle by unknown mechanisms. We found that Polycomb repressive complex 2 (PRC2) subunits are differentially recruited to lineage specifier gene promoters across cell cycle in mouse embryonic stem cells (mESCs). Jarid2 and the catalytic subunit Ezh2 are markedly accumulated at target promoters during S and G(2) phases, while the transcriptionally activating subunits EPOP and EloB are enriched during G(1) phase. Fluctuations in the recruitment of PRC2 subunits promote changes in RNA synthesis and RNA polymerase II binding that are compromised in Jarid2 −/− mESCs. Overall, we show that differential recruitment of PRC2 subunits across cell cycle enables the establishment of a chromatin state that facilitates the induction of cell differentiation in G(1) phase. American Association for the Advancement of Science 2020-03-04 /pmc/articles/PMC7056320/ /pubmed/32181346 http://dx.doi.org/10.1126/sciadv.aay4768 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Asenjo, Helena G.
Gallardo, Amador
López-Onieva, Lourdes
Tejada, Irene
Martorell-Marugán, Jordi
Carmona-Sáez, Pedro
Landeira, David
Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title_full Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title_fullStr Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title_full_unstemmed Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title_short Polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
title_sort polycomb regulation is coupled to cell cycle transition in pluripotent stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056320/
https://www.ncbi.nlm.nih.gov/pubmed/32181346
http://dx.doi.org/10.1126/sciadv.aay4768
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