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Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription

Cdc14 is an essential phosphatase in yeast but its role in the mammalian cell cycle remains obscure. We report here that Cdc14b-knockout cells display unscheduled induction of multiple cell cycle regulators resulting in early entry into DNA replication and mitosis from quiescence. Cdc14b dephosphory...

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Autores principales: Guillamot, María, Manchado, Eusebio, Chiesa, Massimo, Gómez-López, Gonzalo, Pisano, David G., Sacristán, María P., Malumbres, Marcos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240995/
https://www.ncbi.nlm.nih.gov/pubmed/22355704
http://dx.doi.org/10.1038/srep00189
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author Guillamot, María
Manchado, Eusebio
Chiesa, Massimo
Gómez-López, Gonzalo
Pisano, David G.
Sacristán, María P.
Malumbres, Marcos
author_facet Guillamot, María
Manchado, Eusebio
Chiesa, Massimo
Gómez-López, Gonzalo
Pisano, David G.
Sacristán, María P.
Malumbres, Marcos
author_sort Guillamot, María
collection PubMed
description Cdc14 is an essential phosphatase in yeast but its role in the mammalian cell cycle remains obscure. We report here that Cdc14b-knockout cells display unscheduled induction of multiple cell cycle regulators resulting in early entry into DNA replication and mitosis from quiescence. Cdc14b dephosphorylates Ser5 at the C-terminal domain (CTD) of RNA polymerase II, a major substrate of cyclin-dependent kinases. Lack of Cdc14b results in increased CTD-Ser5 phosphorylation, epigenetic modifications that mark active chromatin, and transcriptional induction of cell cycle regulators. These data suggest a function for mammalian Cdc14 phosphatases in the control of transcription during the cell cycle.
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spelling pubmed-32409952011-12-22 Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription Guillamot, María Manchado, Eusebio Chiesa, Massimo Gómez-López, Gonzalo Pisano, David G. Sacristán, María P. Malumbres, Marcos Sci Rep Article Cdc14 is an essential phosphatase in yeast but its role in the mammalian cell cycle remains obscure. We report here that Cdc14b-knockout cells display unscheduled induction of multiple cell cycle regulators resulting in early entry into DNA replication and mitosis from quiescence. Cdc14b dephosphorylates Ser5 at the C-terminal domain (CTD) of RNA polymerase II, a major substrate of cyclin-dependent kinases. Lack of Cdc14b results in increased CTD-Ser5 phosphorylation, epigenetic modifications that mark active chromatin, and transcriptional induction of cell cycle regulators. These data suggest a function for mammalian Cdc14 phosphatases in the control of transcription during the cell cycle. Nature Publishing Group 2011-12-12 /pmc/articles/PMC3240995/ /pubmed/22355704 http://dx.doi.org/10.1038/srep00189 Text en Copyright © 2011, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Guillamot, María
Manchado, Eusebio
Chiesa, Massimo
Gómez-López, Gonzalo
Pisano, David G.
Sacristán, María P.
Malumbres, Marcos
Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title_full Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title_fullStr Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title_full_unstemmed Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title_short Cdc14b regulates mammalian RNA polymerase II and represses cell cycle transcription
title_sort cdc14b regulates mammalian rna polymerase ii and represses cell cycle transcription
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240995/
https://www.ncbi.nlm.nih.gov/pubmed/22355704
http://dx.doi.org/10.1038/srep00189
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