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Reorganization of budding yeast cytoplasm upon energy depletion
Yeast cells, when exposed to stress, can enter a protective state in which cell division, growth, and metabolism are down-regulated. They remain viable in this state until nutrients become available again. How cells enter this protective survival state and what happens at a cellular and subcellular...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353153/ https://www.ncbi.nlm.nih.gov/pubmed/32293990 http://dx.doi.org/10.1091/mbc.E20-02-0125 |
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author | Marini, Guendalina Nüske, Elisabeth Leng, Weihua Alberti, Simon Pigino, Gaia |
author_facet | Marini, Guendalina Nüske, Elisabeth Leng, Weihua Alberti, Simon Pigino, Gaia |
author_sort | Marini, Guendalina |
collection | PubMed |
description | Yeast cells, when exposed to stress, can enter a protective state in which cell division, growth, and metabolism are down-regulated. They remain viable in this state until nutrients become available again. How cells enter this protective survival state and what happens at a cellular and subcellular level are largely unknown. In this study, we used electron tomography to investigate stress-induced ultrastructural changes in the cytoplasm of yeast cells. After ATP depletion, we observed significant cytosolic compaction and extensive cytoplasmic reorganization, as well as the emergence of distinct membrane-bound and membraneless organelles. Using correlative light and electron microscopy, we further demonstrated that one of these membraneless organelles was generated by the reversible polymerization of eukaryotic translation initiation factor 2B, an essential enzyme in the initiation of protein synthesis, into large bundles of filaments. The changes we observe are part of a stress-induced survival strategy, allowing yeast cells to save energy, protect proteins from degradation, and inhibit protein functionality by forming assemblies of proteins. |
format | Online Article Text |
id | pubmed-7353153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73531532020-08-17 Reorganization of budding yeast cytoplasm upon energy depletion Marini, Guendalina Nüske, Elisabeth Leng, Weihua Alberti, Simon Pigino, Gaia Mol Biol Cell Articles Yeast cells, when exposed to stress, can enter a protective state in which cell division, growth, and metabolism are down-regulated. They remain viable in this state until nutrients become available again. How cells enter this protective survival state and what happens at a cellular and subcellular level are largely unknown. In this study, we used electron tomography to investigate stress-induced ultrastructural changes in the cytoplasm of yeast cells. After ATP depletion, we observed significant cytosolic compaction and extensive cytoplasmic reorganization, as well as the emergence of distinct membrane-bound and membraneless organelles. Using correlative light and electron microscopy, we further demonstrated that one of these membraneless organelles was generated by the reversible polymerization of eukaryotic translation initiation factor 2B, an essential enzyme in the initiation of protein synthesis, into large bundles of filaments. The changes we observe are part of a stress-induced survival strategy, allowing yeast cells to save energy, protect proteins from degradation, and inhibit protein functionality by forming assemblies of proteins. The American Society for Cell Biology 2020-06-01 /pmc/articles/PMC7353153/ /pubmed/32293990 http://dx.doi.org/10.1091/mbc.E20-02-0125 Text en © 2020 Marini et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Marini, Guendalina Nüske, Elisabeth Leng, Weihua Alberti, Simon Pigino, Gaia Reorganization of budding yeast cytoplasm upon energy depletion |
title | Reorganization of budding yeast cytoplasm upon energy depletion |
title_full | Reorganization of budding yeast cytoplasm upon energy depletion |
title_fullStr | Reorganization of budding yeast cytoplasm upon energy depletion |
title_full_unstemmed | Reorganization of budding yeast cytoplasm upon energy depletion |
title_short | Reorganization of budding yeast cytoplasm upon energy depletion |
title_sort | reorganization of budding yeast cytoplasm upon energy depletion |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353153/ https://www.ncbi.nlm.nih.gov/pubmed/32293990 http://dx.doi.org/10.1091/mbc.E20-02-0125 |
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