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RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis

Mammalian chromosomes are three-dimensional entities shaped by converging and opposing forces. Mitotic cell division induces marked chromosome condensation, but following reentry into the G(1) phase of the cell cycle, chromosomes reestablish their interphase organization. Here, we tested the role of...

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Autores principales: Zhang, Shu, Übelmesser, Nadine, Josipovic, Natasa, Forte, Giada, Slotman, Johan A., Chiang, Michael, Gothe, Henrike Johanna, Gusmao, Eduardo Gade, Becker, Christian, Altmüller, Janine, Houtsmuller, Adriaan B., Roukos, Vassilis, Wendt, Kerstin S., Marenduzzo, Davide, Papantonis, Argyris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535795/
https://www.ncbi.nlm.nih.gov/pubmed/34678064
http://dx.doi.org/10.1126/sciadv.abg8205
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author Zhang, Shu
Übelmesser, Nadine
Josipovic, Natasa
Forte, Giada
Slotman, Johan A.
Chiang, Michael
Gothe, Henrike Johanna
Gusmao, Eduardo Gade
Becker, Christian
Altmüller, Janine
Houtsmuller, Adriaan B.
Roukos, Vassilis
Wendt, Kerstin S.
Marenduzzo, Davide
Papantonis, Argyris
author_facet Zhang, Shu
Übelmesser, Nadine
Josipovic, Natasa
Forte, Giada
Slotman, Johan A.
Chiang, Michael
Gothe, Henrike Johanna
Gusmao, Eduardo Gade
Becker, Christian
Altmüller, Janine
Houtsmuller, Adriaan B.
Roukos, Vassilis
Wendt, Kerstin S.
Marenduzzo, Davide
Papantonis, Argyris
author_sort Zhang, Shu
collection PubMed
description Mammalian chromosomes are three-dimensional entities shaped by converging and opposing forces. Mitotic cell division induces marked chromosome condensation, but following reentry into the G(1) phase of the cell cycle, chromosomes reestablish their interphase organization. Here, we tested the role of RNA polymerase II (RNAPII) in this transition using a cell line that allows its auxin-mediated degradation. In situ Hi-C showed that RNAPII is required for both compartment and loop establishment following mitosis. RNAPs often counteract loop extrusion, and in their absence, longer and more prominent loops arose. Evidence from chromatin binding, super-resolution imaging, and in silico modeling allude to these effects being a result of RNAPII-mediated cohesin loading upon G(1) reentry. Our findings reconcile the role of RNAPII in gene expression with that in chromatin architecture.
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spelling pubmed-85357952021-11-02 RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis Zhang, Shu Übelmesser, Nadine Josipovic, Natasa Forte, Giada Slotman, Johan A. Chiang, Michael Gothe, Henrike Johanna Gusmao, Eduardo Gade Becker, Christian Altmüller, Janine Houtsmuller, Adriaan B. Roukos, Vassilis Wendt, Kerstin S. Marenduzzo, Davide Papantonis, Argyris Sci Adv Biomedicine and Life Sciences Mammalian chromosomes are three-dimensional entities shaped by converging and opposing forces. Mitotic cell division induces marked chromosome condensation, but following reentry into the G(1) phase of the cell cycle, chromosomes reestablish their interphase organization. Here, we tested the role of RNA polymerase II (RNAPII) in this transition using a cell line that allows its auxin-mediated degradation. In situ Hi-C showed that RNAPII is required for both compartment and loop establishment following mitosis. RNAPs often counteract loop extrusion, and in their absence, longer and more prominent loops arose. Evidence from chromatin binding, super-resolution imaging, and in silico modeling allude to these effects being a result of RNAPII-mediated cohesin loading upon G(1) reentry. Our findings reconcile the role of RNAPII in gene expression with that in chromatin architecture. American Association for the Advancement of Science 2021-10-22 /pmc/articles/PMC8535795/ /pubmed/34678064 http://dx.doi.org/10.1126/sciadv.abg8205 Text en Copyright © 2021 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). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://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 Biomedicine and Life Sciences
Zhang, Shu
Übelmesser, Nadine
Josipovic, Natasa
Forte, Giada
Slotman, Johan A.
Chiang, Michael
Gothe, Henrike Johanna
Gusmao, Eduardo Gade
Becker, Christian
Altmüller, Janine
Houtsmuller, Adriaan B.
Roukos, Vassilis
Wendt, Kerstin S.
Marenduzzo, Davide
Papantonis, Argyris
RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title_full RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title_fullStr RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title_full_unstemmed RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title_short RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis
title_sort rna polymerase ii is required for spatial chromatin reorganization following exit from mitosis
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535795/
https://www.ncbi.nlm.nih.gov/pubmed/34678064
http://dx.doi.org/10.1126/sciadv.abg8205
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