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BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation
In Drosophila, a complex consisting of Calypso and ASX catalyzes H2A deubiquitination and has been reported to act as part of the Polycomb machinery in transcriptional silencing. The mammalian homologs of these proteins (BAP1 and ASXL1/2/3, respectively), are frequently mutated in various cancer typ...
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/PMC6341105/ https://www.ncbi.nlm.nih.gov/pubmed/30664650 http://dx.doi.org/10.1038/s41467-018-08255-x |
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author | Campagne, Antoine Lee, Ming-Kang Zielinski, Dina Michaud, Audrey Le Corre, Stéphanie Dingli, Florent Chen, Hong Shahidian, Lara Z. Vassilev, Ivaylo Servant, Nicolas Loew, Damarys Pasmant, Eric Postel-Vinay, Sophie Wassef, Michel Margueron, Raphaël |
author_facet | Campagne, Antoine Lee, Ming-Kang Zielinski, Dina Michaud, Audrey Le Corre, Stéphanie Dingli, Florent Chen, Hong Shahidian, Lara Z. Vassilev, Ivaylo Servant, Nicolas Loew, Damarys Pasmant, Eric Postel-Vinay, Sophie Wassef, Michel Margueron, Raphaël |
author_sort | Campagne, Antoine |
collection | PubMed |
description | In Drosophila, a complex consisting of Calypso and ASX catalyzes H2A deubiquitination and has been reported to act as part of the Polycomb machinery in transcriptional silencing. The mammalian homologs of these proteins (BAP1 and ASXL1/2/3, respectively), are frequently mutated in various cancer types, yet their precise functions remain unclear. Using an integrative approach based on isogenic cell lines generated with CRISPR/Cas9, we uncover an unanticipated role for BAP1 in gene activation. This function requires the assembly of an enzymatically active BAP1-associated core complex (BAP1.com) containing one of the redundant ASXL proteins. We investigate the mechanism underlying BAP1.com-mediated transcriptional regulation and show that it does not participate in Polycomb-mediated silencing. Instead, our results establish that the function of BAP1.com is to safeguard transcriptionally active genes against silencing by the Polycomb Repressive Complex 1. |
format | Online Article Text |
id | pubmed-6341105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63411052019-01-23 BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation Campagne, Antoine Lee, Ming-Kang Zielinski, Dina Michaud, Audrey Le Corre, Stéphanie Dingli, Florent Chen, Hong Shahidian, Lara Z. Vassilev, Ivaylo Servant, Nicolas Loew, Damarys Pasmant, Eric Postel-Vinay, Sophie Wassef, Michel Margueron, Raphaël Nat Commun Article In Drosophila, a complex consisting of Calypso and ASX catalyzes H2A deubiquitination and has been reported to act as part of the Polycomb machinery in transcriptional silencing. The mammalian homologs of these proteins (BAP1 and ASXL1/2/3, respectively), are frequently mutated in various cancer types, yet their precise functions remain unclear. Using an integrative approach based on isogenic cell lines generated with CRISPR/Cas9, we uncover an unanticipated role for BAP1 in gene activation. This function requires the assembly of an enzymatically active BAP1-associated core complex (BAP1.com) containing one of the redundant ASXL proteins. We investigate the mechanism underlying BAP1.com-mediated transcriptional regulation and show that it does not participate in Polycomb-mediated silencing. Instead, our results establish that the function of BAP1.com is to safeguard transcriptionally active genes against silencing by the Polycomb Repressive Complex 1. Nature Publishing Group UK 2019-01-21 /pmc/articles/PMC6341105/ /pubmed/30664650 http://dx.doi.org/10.1038/s41467-018-08255-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 Campagne, Antoine Lee, Ming-Kang Zielinski, Dina Michaud, Audrey Le Corre, Stéphanie Dingli, Florent Chen, Hong Shahidian, Lara Z. Vassilev, Ivaylo Servant, Nicolas Loew, Damarys Pasmant, Eric Postel-Vinay, Sophie Wassef, Michel Margueron, Raphaël BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title | BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title_full | BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title_fullStr | BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title_full_unstemmed | BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title_short | BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation |
title_sort | bap1 complex promotes transcription by opposing prc1-mediated h2a ubiquitylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341105/ https://www.ncbi.nlm.nih.gov/pubmed/30664650 http://dx.doi.org/10.1038/s41467-018-08255-x |
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