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Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts

Delineating the strategies by which cells contend with combinatorial changing environments is crucial for understanding cellular regulatory organization. When presented with two carbon sources, microorganisms first consume the carbon substrate that supports the highest growth rate (e.g., glucose) an...

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Autores principales: Venturelli, Ophelia S., Zuleta, Ignacio, Murray, Richard M., El-Samad, Hana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307983/
https://www.ncbi.nlm.nih.gov/pubmed/25626086
http://dx.doi.org/10.1371/journal.pbio.1002042
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author Venturelli, Ophelia S.
Zuleta, Ignacio
Murray, Richard M.
El-Samad, Hana
author_facet Venturelli, Ophelia S.
Zuleta, Ignacio
Murray, Richard M.
El-Samad, Hana
author_sort Venturelli, Ophelia S.
collection PubMed
description Delineating the strategies by which cells contend with combinatorial changing environments is crucial for understanding cellular regulatory organization. When presented with two carbon sources, microorganisms first consume the carbon substrate that supports the highest growth rate (e.g., glucose) and then switch to the secondary carbon source (e.g., galactose), a paradigm known as the Monod model. Sequential sugar utilization has been attributed to transcriptional repression of the secondary metabolic pathway, followed by activation of this pathway upon depletion of the preferred carbon source. In this work, we demonstrate that although Saccharomyces cerevisiae cells consume glucose before galactose, the galactose regulatory pathway is activated in a fraction of the cell population hours before glucose is fully consumed. This early activation reduces the time required for the population to transition between the two metabolic programs and provides a fitness advantage that might be crucial in competitive environments.
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spelling pubmed-43079832015-02-06 Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts Venturelli, Ophelia S. Zuleta, Ignacio Murray, Richard M. El-Samad, Hana PLoS Biol Research Article Delineating the strategies by which cells contend with combinatorial changing environments is crucial for understanding cellular regulatory organization. When presented with two carbon sources, microorganisms first consume the carbon substrate that supports the highest growth rate (e.g., glucose) and then switch to the secondary carbon source (e.g., galactose), a paradigm known as the Monod model. Sequential sugar utilization has been attributed to transcriptional repression of the secondary metabolic pathway, followed by activation of this pathway upon depletion of the preferred carbon source. In this work, we demonstrate that although Saccharomyces cerevisiae cells consume glucose before galactose, the galactose regulatory pathway is activated in a fraction of the cell population hours before glucose is fully consumed. This early activation reduces the time required for the population to transition between the two metabolic programs and provides a fitness advantage that might be crucial in competitive environments. Public Library of Science 2015-01-27 /pmc/articles/PMC4307983/ /pubmed/25626086 http://dx.doi.org/10.1371/journal.pbio.1002042 Text en © 2015 Venturelli et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Venturelli, Ophelia S.
Zuleta, Ignacio
Murray, Richard M.
El-Samad, Hana
Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title_full Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title_fullStr Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title_full_unstemmed Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title_short Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
title_sort population diversification in a yeast metabolic program promotes anticipation of environmental shifts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307983/
https://www.ncbi.nlm.nih.gov/pubmed/25626086
http://dx.doi.org/10.1371/journal.pbio.1002042
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