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A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit

Cells perpetually face the decision to proliferate or to stay quiescent. Here we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange both their actin and microtubule (MT) cytoskeletons and lose their polarity. Indeed, while polarity markers are lost from ce...

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Autores principales: Laporte, Damien, Courtout, Fabien, Pinson, Benoît, Dompierre, Jim, Salin, Bénédicte, Brocard, Lysiane, Sagot, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494004/
https://www.ncbi.nlm.nih.gov/pubmed/26124291
http://dx.doi.org/10.1083/jcb.201502025
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author Laporte, Damien
Courtout, Fabien
Pinson, Benoît
Dompierre, Jim
Salin, Bénédicte
Brocard, Lysiane
Sagot, Isabelle
author_facet Laporte, Damien
Courtout, Fabien
Pinson, Benoît
Dompierre, Jim
Salin, Bénédicte
Brocard, Lysiane
Sagot, Isabelle
author_sort Laporte, Damien
collection PubMed
description Cells perpetually face the decision to proliferate or to stay quiescent. Here we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange both their actin and microtubule (MT) cytoskeletons and lose their polarity. Indeed, while polarity markers are lost from cell extremities, actin patches and cables are reorganized into actin bodies, which are stable actin filament–containing structures. Astonishingly, MTs are also stabilized and rearranged into a novel antiparallel bundle associated with the spindle pole body, named Q-MT bundle. We have identified proteins involved in this process and propose a molecular model for Q-MT bundle formation. Finally and importantly, we reveal that Q-MT bundle elongation is involved in polarity reestablishment upon quiescence exit and thereby the efficient return to the proliferative state. Our work demonstrates that quiescent S. pombe cells assemble specific cytoskeleton structures that improve the swiftness of the transition back to proliferation.
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spelling pubmed-44940042016-01-06 A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit Laporte, Damien Courtout, Fabien Pinson, Benoît Dompierre, Jim Salin, Bénédicte Brocard, Lysiane Sagot, Isabelle J Cell Biol Research Articles Cells perpetually face the decision to proliferate or to stay quiescent. Here we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange both their actin and microtubule (MT) cytoskeletons and lose their polarity. Indeed, while polarity markers are lost from cell extremities, actin patches and cables are reorganized into actin bodies, which are stable actin filament–containing structures. Astonishingly, MTs are also stabilized and rearranged into a novel antiparallel bundle associated with the spindle pole body, named Q-MT bundle. We have identified proteins involved in this process and propose a molecular model for Q-MT bundle formation. Finally and importantly, we reveal that Q-MT bundle elongation is involved in polarity reestablishment upon quiescence exit and thereby the efficient return to the proliferative state. Our work demonstrates that quiescent S. pombe cells assemble specific cytoskeleton structures that improve the swiftness of the transition back to proliferation. The Rockefeller University Press 2015-07-06 /pmc/articles/PMC4494004/ /pubmed/26124291 http://dx.doi.org/10.1083/jcb.201502025 Text en © 2015 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
Courtout, Fabien
Pinson, Benoît
Dompierre, Jim
Salin, Bénédicte
Brocard, Lysiane
Sagot, Isabelle
A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title_full A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title_fullStr A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title_full_unstemmed A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title_short A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
title_sort stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494004/
https://www.ncbi.nlm.nih.gov/pubmed/26124291
http://dx.doi.org/10.1083/jcb.201502025
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