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Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes
Polycomb repressive complexes-1 and -2 (PRC1 and 2) silence developmental genes in a spatiotemporal manner during embryogenesis. How Polycomb group (PcG) proteins orchestrate down-regulation of target genes upon differentiation, however, remains elusive. Here, by differentiating embryonic stem cells...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429492/ https://www.ncbi.nlm.nih.gov/pubmed/34504070 http://dx.doi.org/10.1038/s41467-021-24894-z |
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author | Sugishita, Hiroki Kondo, Takashi Ito, Shinsuke Nakayama, Manabu Yakushiji-Kaminatsui, Nayuta Kawakami, Eiryo Koseki, Yoko Ohinata, Yasuhide Sharif, Jafar Harachi, Mio Blackledge, Neil P. Klose, Robert J. Koseki, Haruhiko |
author_facet | Sugishita, Hiroki Kondo, Takashi Ito, Shinsuke Nakayama, Manabu Yakushiji-Kaminatsui, Nayuta Kawakami, Eiryo Koseki, Yoko Ohinata, Yasuhide Sharif, Jafar Harachi, Mio Blackledge, Neil P. Klose, Robert J. Koseki, Haruhiko |
author_sort | Sugishita, Hiroki |
collection | PubMed |
description | Polycomb repressive complexes-1 and -2 (PRC1 and 2) silence developmental genes in a spatiotemporal manner during embryogenesis. How Polycomb group (PcG) proteins orchestrate down-regulation of target genes upon differentiation, however, remains elusive. Here, by differentiating embryonic stem cells into embryoid bodies, we reveal a crucial role for the PCGF1-containing variant PRC1 complex (PCGF1-PRC1) to mediate differentiation-associated down-regulation of a group of genes. Upon differentiation cues, transcription is down-regulated at these genes, in association with PCGF1-PRC1-mediated deposition of histone H2AK119 mono-ubiquitination (H2AK119ub1) and PRC2 recruitment. In the absence of PCGF1-PRC1, both H2AK119ub1 deposition and PRC2 recruitment are disrupted, leading to aberrant expression of target genes. PCGF1-PRC1 is, therefore, required for initiation and consolidation of PcG-mediated gene repression during differentiation. |
format | Online Article Text |
id | pubmed-8429492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84294922021-09-24 Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes Sugishita, Hiroki Kondo, Takashi Ito, Shinsuke Nakayama, Manabu Yakushiji-Kaminatsui, Nayuta Kawakami, Eiryo Koseki, Yoko Ohinata, Yasuhide Sharif, Jafar Harachi, Mio Blackledge, Neil P. Klose, Robert J. Koseki, Haruhiko Nat Commun Article Polycomb repressive complexes-1 and -2 (PRC1 and 2) silence developmental genes in a spatiotemporal manner during embryogenesis. How Polycomb group (PcG) proteins orchestrate down-regulation of target genes upon differentiation, however, remains elusive. Here, by differentiating embryonic stem cells into embryoid bodies, we reveal a crucial role for the PCGF1-containing variant PRC1 complex (PCGF1-PRC1) to mediate differentiation-associated down-regulation of a group of genes. Upon differentiation cues, transcription is down-regulated at these genes, in association with PCGF1-PRC1-mediated deposition of histone H2AK119 mono-ubiquitination (H2AK119ub1) and PRC2 recruitment. In the absence of PCGF1-PRC1, both H2AK119ub1 deposition and PRC2 recruitment are disrupted, leading to aberrant expression of target genes. PCGF1-PRC1 is, therefore, required for initiation and consolidation of PcG-mediated gene repression during differentiation. Nature Publishing Group UK 2021-09-09 /pmc/articles/PMC8429492/ /pubmed/34504070 http://dx.doi.org/10.1038/s41467-021-24894-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sugishita, Hiroki Kondo, Takashi Ito, Shinsuke Nakayama, Manabu Yakushiji-Kaminatsui, Nayuta Kawakami, Eiryo Koseki, Yoko Ohinata, Yasuhide Sharif, Jafar Harachi, Mio Blackledge, Neil P. Klose, Robert J. Koseki, Haruhiko Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title | Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title_full | Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title_fullStr | Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title_full_unstemmed | Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title_short | Variant PCGF1-PRC1 links PRC2 recruitment with differentiation-associated transcriptional inactivation at target genes |
title_sort | variant pcgf1-prc1 links prc2 recruitment with differentiation-associated transcriptional inactivation at target genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429492/ https://www.ncbi.nlm.nih.gov/pubmed/34504070 http://dx.doi.org/10.1038/s41467-021-24894-z |
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