Cohesin Removal Reprograms Gene Expression upon Mitotic Entry

© 2020 Elsevier Inc. As cells enter mitosis, the genome is restructured to facilitate chromosome segregation, accompanied by dramatic changes in gene expression. However, the mechanisms that underlie mitotic transcriptional regulation are unclear. In contrast to transcribed genes, centromere regions...

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Main Authors: Perea-Resa, Carlos, Bury, Leah, Cheeseman, Iain M, Blower, Michael D
Format: Article
Language:English
Published: Elsevier BV 2021
Online Access:https://hdl.handle.net/1721.1/136229
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author Perea-Resa, Carlos
Bury, Leah
Cheeseman, Iain M
Blower, Michael D
author_facet Perea-Resa, Carlos
Bury, Leah
Cheeseman, Iain M
Blower, Michael D
author_sort Perea-Resa, Carlos
collection MIT
description © 2020 Elsevier Inc. As cells enter mitosis, the genome is restructured to facilitate chromosome segregation, accompanied by dramatic changes in gene expression. However, the mechanisms that underlie mitotic transcriptional regulation are unclear. In contrast to transcribed genes, centromere regions retain transcriptionally active RNA polymerase II (Pol II) in mitosis. Here, we demonstrate that chromatin-bound cohesin is necessary to retain elongating Pol II at centromeres. We find that WAPL-mediated removal of cohesin from chromosome arms during prophase is required for the dissociation of Pol II and nascent transcripts, and failure of this process dramatically alters mitotic gene expression. Removal of cohesin/Pol II from chromosome arms in prophase is important for accurate chromosome segregation and normal activation of gene expression in G1. We propose that prophase cohesin removal is a key step in reprogramming gene expression as cells transition from G2 through mitosis to G1.
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spelling mit-1721.1/1362292021-10-28T04:02:16Z Cohesin Removal Reprograms Gene Expression upon Mitotic Entry Perea-Resa, Carlos Bury, Leah Cheeseman, Iain M Blower, Michael D © 2020 Elsevier Inc. As cells enter mitosis, the genome is restructured to facilitate chromosome segregation, accompanied by dramatic changes in gene expression. However, the mechanisms that underlie mitotic transcriptional regulation are unclear. In contrast to transcribed genes, centromere regions retain transcriptionally active RNA polymerase II (Pol II) in mitosis. Here, we demonstrate that chromatin-bound cohesin is necessary to retain elongating Pol II at centromeres. We find that WAPL-mediated removal of cohesin from chromosome arms during prophase is required for the dissociation of Pol II and nascent transcripts, and failure of this process dramatically alters mitotic gene expression. Removal of cohesin/Pol II from chromosome arms in prophase is important for accurate chromosome segregation and normal activation of gene expression in G1. We propose that prophase cohesin removal is a key step in reprogramming gene expression as cells transition from G2 through mitosis to G1. 2021-10-27T20:34:22Z 2021-10-27T20:34:22Z 2020 2021-07-14T17:31:48Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/136229 en 10.1016/J.MOLCEL.2020.01.023 Molecular Cell Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier BV PMC
spellingShingle Perea-Resa, Carlos
Bury, Leah
Cheeseman, Iain M
Blower, Michael D
Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title_full Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title_fullStr Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title_full_unstemmed Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title_short Cohesin Removal Reprograms Gene Expression upon Mitotic Entry
title_sort cohesin removal reprograms gene expression upon mitotic entry
url https://hdl.handle.net/1721.1/136229
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AT buryleah cohesinremovalreprogramsgeneexpressionuponmitoticentry
AT cheesemaniainm cohesinremovalreprogramsgeneexpressionuponmitoticentry
AT blowermichaeld cohesinremovalreprogramsgeneexpressionuponmitoticentry