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Metabolic status rather than cell cycle signals control quiescence entry and exit
Quiescence is defined as a temporary arrest of proliferation, yet it likely encompasses various cellular situations. Our knowledge about this widespread cellular state remains limited. In particular, little is known about the molecular determinants that orchestrate quiescence establishment and exit....
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063145/ https://www.ncbi.nlm.nih.gov/pubmed/21402786 http://dx.doi.org/10.1083/jcb.201009028 |
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author | Laporte, Damien Lebaudy, Anne Sahin, Annelise Pinson, Benoît Ceschin, Johanna Daignan-Fornier, Bertrand Sagot, Isabelle |
author_facet | Laporte, Damien Lebaudy, Anne Sahin, Annelise Pinson, Benoît Ceschin, Johanna Daignan-Fornier, Bertrand Sagot, Isabelle |
author_sort | Laporte, Damien |
collection | PubMed |
description | Quiescence is defined as a temporary arrest of proliferation, yet it likely encompasses various cellular situations. Our knowledge about this widespread cellular state remains limited. In particular, little is known about the molecular determinants that orchestrate quiescence establishment and exit. Here we show that upon carbon source exhaustion, budding yeast can enter quiescence from all cell cycle phases. Moreover, using cellular structures that are candidate markers for quiescence, we found that the first steps of quiescence exit can be triggered independently of cell growth and proliferation by the sole addition of glucose in both Saccharomyces cerevisiae and Schizosaccharomyces pombe. Importantly, glucose needs to be internalized and catabolized all the way down to glycolysis to mobilize quiescent cell specific structures, but, strikingly, ATP replenishment is apparently not the key signal. Altogether, these findings strongly suggest that quiescence entry and exit primarily rely on cellular metabolic status and can be uncoupled from the cell cycle. |
format | Text |
id | pubmed-3063145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30631452011-09-21 Metabolic status rather than cell cycle signals control quiescence entry and exit Laporte, Damien Lebaudy, Anne Sahin, Annelise Pinson, Benoît Ceschin, Johanna Daignan-Fornier, Bertrand Sagot, Isabelle J Cell Biol Research Articles Quiescence is defined as a temporary arrest of proliferation, yet it likely encompasses various cellular situations. Our knowledge about this widespread cellular state remains limited. In particular, little is known about the molecular determinants that orchestrate quiescence establishment and exit. Here we show that upon carbon source exhaustion, budding yeast can enter quiescence from all cell cycle phases. Moreover, using cellular structures that are candidate markers for quiescence, we found that the first steps of quiescence exit can be triggered independently of cell growth and proliferation by the sole addition of glucose in both Saccharomyces cerevisiae and Schizosaccharomyces pombe. Importantly, glucose needs to be internalized and catabolized all the way down to glycolysis to mobilize quiescent cell specific structures, but, strikingly, ATP replenishment is apparently not the key signal. Altogether, these findings strongly suggest that quiescence entry and exit primarily rely on cellular metabolic status and can be uncoupled from the cell cycle. The Rockefeller University Press 2011-03-21 /pmc/articles/PMC3063145/ /pubmed/21402786 http://dx.doi.org/10.1083/jcb.201009028 Text en © 2011 Laporte et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Laporte, Damien Lebaudy, Anne Sahin, Annelise Pinson, Benoît Ceschin, Johanna Daignan-Fornier, Bertrand Sagot, Isabelle Metabolic status rather than cell cycle signals control quiescence entry and exit |
title | Metabolic status rather than cell cycle signals control quiescence entry and exit |
title_full | Metabolic status rather than cell cycle signals control quiescence entry and exit |
title_fullStr | Metabolic status rather than cell cycle signals control quiescence entry and exit |
title_full_unstemmed | Metabolic status rather than cell cycle signals control quiescence entry and exit |
title_short | Metabolic status rather than cell cycle signals control quiescence entry and exit |
title_sort | metabolic status rather than cell cycle signals control quiescence entry and exit |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063145/ https://www.ncbi.nlm.nih.gov/pubmed/21402786 http://dx.doi.org/10.1083/jcb.201009028 |
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