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Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation
Cells depend on a highly ordered organisation of their content and must develop strategies to maintain the anisotropic distribution of organelles during periods of nutrient shortage. One of these strategies is to solidify the cytoplasm, which was observed in bacteria and yeast cells with acutely int...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857596/ https://www.ncbi.nlm.nih.gov/pubmed/31558680 http://dx.doi.org/10.1242/jcs.231688 |
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author | Heimlicher, Maria B. Bächler, Mirjam Liu, Minghua Ibeneche-Nnewihe, Chieze Florin, Ernst-Ludwig Hoenger, Andreas Brunner, Damian |
author_facet | Heimlicher, Maria B. Bächler, Mirjam Liu, Minghua Ibeneche-Nnewihe, Chieze Florin, Ernst-Ludwig Hoenger, Andreas Brunner, Damian |
author_sort | Heimlicher, Maria B. |
collection | PubMed |
description | Cells depend on a highly ordered organisation of their content and must develop strategies to maintain the anisotropic distribution of organelles during periods of nutrient shortage. One of these strategies is to solidify the cytoplasm, which was observed in bacteria and yeast cells with acutely interrupted energy production. Here, we describe a different type of cytoplasm solidification fission yeast cells switch to, after having run out of nutrients during multiple days in culture. It provides the most profound reversible cytoplasmic solidification of yeast cells described to date. Our data exclude the previously proposed mechanisms for cytoplasm solidification in yeasts and suggest a mechanism that immobilises cellular components in a size-dependent manner. We provide experimental evidence that, in addition to time, cells use intrinsic nutrients and energy sources to reach this state. Such cytoplasmic solidification may provide a robust means to protect cellular architecture in dormant cells. |
format | Online Article Text |
id | pubmed-6857596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68575962019-11-21 Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation Heimlicher, Maria B. Bächler, Mirjam Liu, Minghua Ibeneche-Nnewihe, Chieze Florin, Ernst-Ludwig Hoenger, Andreas Brunner, Damian J Cell Sci Research Article Cells depend on a highly ordered organisation of their content and must develop strategies to maintain the anisotropic distribution of organelles during periods of nutrient shortage. One of these strategies is to solidify the cytoplasm, which was observed in bacteria and yeast cells with acutely interrupted energy production. Here, we describe a different type of cytoplasm solidification fission yeast cells switch to, after having run out of nutrients during multiple days in culture. It provides the most profound reversible cytoplasmic solidification of yeast cells described to date. Our data exclude the previously proposed mechanisms for cytoplasm solidification in yeasts and suggest a mechanism that immobilises cellular components in a size-dependent manner. We provide experimental evidence that, in addition to time, cells use intrinsic nutrients and energy sources to reach this state. Such cytoplasmic solidification may provide a robust means to protect cellular architecture in dormant cells. The Company of Biologists Ltd 2019-11-01 2019-11-08 /pmc/articles/PMC6857596/ /pubmed/31558680 http://dx.doi.org/10.1242/jcs.231688 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Heimlicher, Maria B. Bächler, Mirjam Liu, Minghua Ibeneche-Nnewihe, Chieze Florin, Ernst-Ludwig Hoenger, Andreas Brunner, Damian Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title | Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title_full | Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title_fullStr | Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title_full_unstemmed | Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title_short | Reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
title_sort | reversible solidification of fission yeast cytoplasm after prolonged nutrient starvation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857596/ https://www.ncbi.nlm.nih.gov/pubmed/31558680 http://dx.doi.org/10.1242/jcs.231688 |
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