Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784587869957914624 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8535795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhangshu rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT ubelmessernadine rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT josipovicnatasa rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT fortegiada rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT slotmanjohana rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT chiangmichael rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT gothehenrikejohanna rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT gusmaoeduardogade rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT beckerchristian rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT altmullerjanine rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT houtsmulleradriaanb rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT roukosvassilis rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT wendtkerstins rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT marenduzzodavide rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis AT papantonisargyris rnapolymeraseiiisrequiredforspatialchromatinreorganizationfollowingexitfrommitosis |