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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4494004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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