DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression

Cell cycle arrest after DNA damage is achieved by the expression of the CDK inhibitor p21. Here the authors show that spontaneous DNA damage incurred in unperturbed cell cycles, leads to cell populations exhibiting a bistable state, with p53 and p21 regulating the proliferation-quiescence decision.

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Autores principales: Alexis R. Barr, Samuel Cooper, Frank S. Heldt, Francesca Butera, Henriette Stoy, Jörg Mansfeld, Béla Novák, Chris Bakal
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/afa56ee404454f3788fc31b2ea96dc7a
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spelling oai:doaj.org-article:afa56ee404454f3788fc31b2ea96dc7a2021-12-02T14:42:18ZDNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression10.1038/ncomms147282041-1723https://doaj.org/article/afa56ee404454f3788fc31b2ea96dc7a2017-03-01T00:00:00Zhttps://doi.org/10.1038/ncomms14728https://doaj.org/toc/2041-1723Cell cycle arrest after DNA damage is achieved by the expression of the CDK inhibitor p21. Here the authors show that spontaneous DNA damage incurred in unperturbed cell cycles, leads to cell populations exhibiting a bistable state, with p53 and p21 regulating the proliferation-quiescence decision.Alexis R. BarrSamuel CooperFrank S. HeldtFrancesca ButeraHenriette StoyJörg MansfeldBéla NovákChris BakalNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Alexis R. Barr
Samuel Cooper
Frank S. Heldt
Francesca Butera
Henriette Stoy
Jörg Mansfeld
Béla Novák
Chris Bakal
DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
description Cell cycle arrest after DNA damage is achieved by the expression of the CDK inhibitor p21. Here the authors show that spontaneous DNA damage incurred in unperturbed cell cycles, leads to cell populations exhibiting a bistable state, with p53 and p21 regulating the proliferation-quiescence decision.
format article
author Alexis R. Barr
Samuel Cooper
Frank S. Heldt
Francesca Butera
Henriette Stoy
Jörg Mansfeld
Béla Novák
Chris Bakal
author_facet Alexis R. Barr
Samuel Cooper
Frank S. Heldt
Francesca Butera
Henriette Stoy
Jörg Mansfeld
Béla Novák
Chris Bakal
author_sort Alexis R. Barr
title DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
title_short DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
title_full DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
title_fullStr DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
title_full_unstemmed DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression
title_sort dna damage during s-phase mediates the proliferation-quiescence decision in the subsequent g1 via p21 expression
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/afa56ee404454f3788fc31b2ea96dc7a
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