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Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources
Cells constantly adapt to environmental fluctuations. These physiological changes require time and therefore cause a lag phase during which the cells do not function optimally. Interestingly, past exposure to an environmental condition can shorten the time needed to adapt when the condition re-occur...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211830/ https://www.ncbi.nlm.nih.gov/pubmed/30299256 http://dx.doi.org/10.7554/eLife.39234 |
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author | Cerulus, Bram Jariani, Abbas Perez-Samper, Gemma Vermeersch, Lieselotte Pietsch, Julian MJ Crane, Matthew M New, Aaron M Gallone, Brigida Roncoroni, Miguel Dzialo, Maria C Govers, Sander K Hendrickx, Jhana O Galle, Eva Coomans, Maarten Berden, Pieter Verbandt, Sara Swain, Peter S Verstrepen, Kevin J |
author_facet | Cerulus, Bram Jariani, Abbas Perez-Samper, Gemma Vermeersch, Lieselotte Pietsch, Julian MJ Crane, Matthew M New, Aaron M Gallone, Brigida Roncoroni, Miguel Dzialo, Maria C Govers, Sander K Hendrickx, Jhana O Galle, Eva Coomans, Maarten Berden, Pieter Verbandt, Sara Swain, Peter S Verstrepen, Kevin J |
author_sort | Cerulus, Bram |
collection | PubMed |
description | Cells constantly adapt to environmental fluctuations. These physiological changes require time and therefore cause a lag phase during which the cells do not function optimally. Interestingly, past exposure to an environmental condition can shorten the time needed to adapt when the condition re-occurs, even in daughter cells that never directly encountered the initial condition. Here, we use the molecular toolbox of Saccharomyces cerevisiae to systematically unravel the molecular mechanism underlying such history-dependent behavior in transitions between glucose and maltose. In contrast to previous hypotheses, the behavior does not depend on persistence of proteins involved in metabolism of a specific sugar. Instead, presence of glucose induces a gradual decline in the cells’ ability to activate respiration, which is needed to metabolize alternative carbon sources. These results reveal how trans-generational transitions in central carbon metabolism generate history-dependent behavior in yeast, and provide a mechanistic framework for similar phenomena in other cell types. |
format | Online Article Text |
id | pubmed-6211830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62118302018-11-07 Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources Cerulus, Bram Jariani, Abbas Perez-Samper, Gemma Vermeersch, Lieselotte Pietsch, Julian MJ Crane, Matthew M New, Aaron M Gallone, Brigida Roncoroni, Miguel Dzialo, Maria C Govers, Sander K Hendrickx, Jhana O Galle, Eva Coomans, Maarten Berden, Pieter Verbandt, Sara Swain, Peter S Verstrepen, Kevin J eLife Computational and Systems Biology Cells constantly adapt to environmental fluctuations. These physiological changes require time and therefore cause a lag phase during which the cells do not function optimally. Interestingly, past exposure to an environmental condition can shorten the time needed to adapt when the condition re-occurs, even in daughter cells that never directly encountered the initial condition. Here, we use the molecular toolbox of Saccharomyces cerevisiae to systematically unravel the molecular mechanism underlying such history-dependent behavior in transitions between glucose and maltose. In contrast to previous hypotheses, the behavior does not depend on persistence of proteins involved in metabolism of a specific sugar. Instead, presence of glucose induces a gradual decline in the cells’ ability to activate respiration, which is needed to metabolize alternative carbon sources. These results reveal how trans-generational transitions in central carbon metabolism generate history-dependent behavior in yeast, and provide a mechanistic framework for similar phenomena in other cell types. eLife Sciences Publications, Ltd 2018-10-09 /pmc/articles/PMC6211830/ /pubmed/30299256 http://dx.doi.org/10.7554/eLife.39234 Text en © 2018, Cerulus et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Cerulus, Bram Jariani, Abbas Perez-Samper, Gemma Vermeersch, Lieselotte Pietsch, Julian MJ Crane, Matthew M New, Aaron M Gallone, Brigida Roncoroni, Miguel Dzialo, Maria C Govers, Sander K Hendrickx, Jhana O Galle, Eva Coomans, Maarten Berden, Pieter Verbandt, Sara Swain, Peter S Verstrepen, Kevin J Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title | Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title_full | Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title_fullStr | Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title_full_unstemmed | Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title_short | Transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
title_sort | transition between fermentation and respiration determines history-dependent behavior in fluctuating carbon sources |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211830/ https://www.ncbi.nlm.nih.gov/pubmed/30299256 http://dx.doi.org/10.7554/eLife.39234 |
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