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A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch

Microbial populations adapt to environmental fluctuations through random switching of fitness-related traits in individual cells. This increases the likelihood that a subpopulation will be adaptive in a future milieu. However, populations are particularly challenged when several environment factors...

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Detalles Bibliográficos
Autores principales: Møller, Henrik D., Andersen, Kaj S., Regenberg, Birgitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656021/
https://www.ncbi.nlm.nih.gov/pubmed/23713139
http://dx.doi.org/10.4161/cib.23933
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author Møller, Henrik D.
Andersen, Kaj S.
Regenberg, Birgitte
author_facet Møller, Henrik D.
Andersen, Kaj S.
Regenberg, Birgitte
author_sort Møller, Henrik D.
collection PubMed
description Microbial populations adapt to environmental fluctuations through random switching of fitness-related traits in individual cells. This increases the likelihood that a subpopulation will be adaptive in a future milieu. However, populations are particularly challenged when several environment factors change simultaneously. We suggest that a population can rapidly adapt to multiple environmental changes if individual members stochastically flip a hub-switch that controls a set of adaptive phenotypes in a single event. This mechanism of coupling phenotypic outcomes via a hub-switch can protect a population against large fluctuations in size. Here we report that the general amino acid transporter Gap1 is a potential hub-switch. The GAP1 gene is flanked by two direct repeats that can lead to GAP1 deletions (∆gap1) and a self-replicating GAP1 circle. Thus, an isogenic GAP1 population can differentiate into two variant, reversible genotypes, ∆gap1 or GAP1(circle). These subpopulations have different phenotypic advantages. A ∆gap1 population has a selective advantage on allantoin or ammonium as a nitrogen source and high stress tolerance. Advantages of the GAP1 population include amino acid uptake, fast energy recruitment by trehalose mobilization, and in some cases, adherent biofilm growth. Our proposed model of a hub-switch locus enhances the bet-hedging model of population dynamics.
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spelling pubmed-36560212013-05-24 A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch Møller, Henrik D. Andersen, Kaj S. Regenberg, Birgitte Commun Integr Biol Article Addendum Microbial populations adapt to environmental fluctuations through random switching of fitness-related traits in individual cells. This increases the likelihood that a subpopulation will be adaptive in a future milieu. However, populations are particularly challenged when several environment factors change simultaneously. We suggest that a population can rapidly adapt to multiple environmental changes if individual members stochastically flip a hub-switch that controls a set of adaptive phenotypes in a single event. This mechanism of coupling phenotypic outcomes via a hub-switch can protect a population against large fluctuations in size. Here we report that the general amino acid transporter Gap1 is a potential hub-switch. The GAP1 gene is flanked by two direct repeats that can lead to GAP1 deletions (∆gap1) and a self-replicating GAP1 circle. Thus, an isogenic GAP1 population can differentiate into two variant, reversible genotypes, ∆gap1 or GAP1(circle). These subpopulations have different phenotypic advantages. A ∆gap1 population has a selective advantage on allantoin or ammonium as a nitrogen source and high stress tolerance. Advantages of the GAP1 population include amino acid uptake, fast energy recruitment by trehalose mobilization, and in some cases, adherent biofilm growth. Our proposed model of a hub-switch locus enhances the bet-hedging model of population dynamics. Landes Bioscience 2013-05-01 2013-04-09 /pmc/articles/PMC3656021/ /pubmed/23713139 http://dx.doi.org/10.4161/cib.23933 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Article Addendum
Møller, Henrik D.
Andersen, Kaj S.
Regenberg, Birgitte
A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title_full A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title_fullStr A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title_full_unstemmed A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title_short A model for generating several adaptive phenotypes from a single genetic event: Saccharomyces cerevisiae GAP1 as a potential bet-hedging switch
title_sort model for generating several adaptive phenotypes from a single genetic event: saccharomyces cerevisiae gap1 as a potential bet-hedging switch
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656021/
https://www.ncbi.nlm.nih.gov/pubmed/23713139
http://dx.doi.org/10.4161/cib.23933
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