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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7056320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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