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...

Descripción completa

Detalles Bibliográficos
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
Descripción
Sumario: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.