Cargando…

An Integrative Model of Ion Regulation in Yeast

Yeast cells are able to tolerate and adapt to a variety of environmental stresses. An essential aspect of stress adaptation is the regulation of monovalent ion concentrations. Ion regulation determines many fundamental physiological parameters, such as cell volume, membrane potential, and intracellu...

Descripción completa

Detalles Bibliográficos
Autores principales: Ke, Ruian, Ingram, Piers J., Haynes, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547829/
https://www.ncbi.nlm.nih.gov/pubmed/23341767
http://dx.doi.org/10.1371/journal.pcbi.1002879
_version_ 1782256238006894592
author Ke, Ruian
Ingram, Piers J.
Haynes, Ken
author_facet Ke, Ruian
Ingram, Piers J.
Haynes, Ken
author_sort Ke, Ruian
collection PubMed
description Yeast cells are able to tolerate and adapt to a variety of environmental stresses. An essential aspect of stress adaptation is the regulation of monovalent ion concentrations. Ion regulation determines many fundamental physiological parameters, such as cell volume, membrane potential, and intracellular pH. It is achieved through the concerted activities of multiple cellular components, including ion transporters and signaling molecules, on both short and long time scales. Although each component has been studied in detail previously, it remains unclear how the physiological parameters are maintained and regulated by the concerted action of all components under a diverse range of stress conditions. In this study, we have constructed an integrated mathematical model of ion regulation in Saccharomyces cerevisiae to understand this coordinated adaptation process. Using this model, we first predict that the interaction between phosphorylated Hog1p and Tok1p at the plasma membrane inhibits Tok1p activity and consequently reduces Na(+) influx under NaCl stress. We further characterize the impacts of NaCl, sorbitol, KCl and alkaline pH stresses on the cellular physiology and the differences between the cellular responses to these stresses. We predict that the calcineurin pathway is essential for maintaining a non-toxic level of intracellular Na(+) in the long-term adaptation to NaCl stress, but that its activation is not required for maintaining a low level of Na(+) under other stresses investigated. We provide evidence that, in addition to extrusion of toxic ions, Ena1p plays an important role, in some cases alongside Nha1p, in re-establishing membrane potential after stress perturbation. To conclude, this model serves as a powerful tool for both understanding the complex system-level properties of the highly coordinated adaptation process and generating further hypotheses for experimental investigation.
format Online
Article
Text
id pubmed-3547829
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35478292013-01-22 An Integrative Model of Ion Regulation in Yeast Ke, Ruian Ingram, Piers J. Haynes, Ken PLoS Comput Biol Research Article Yeast cells are able to tolerate and adapt to a variety of environmental stresses. An essential aspect of stress adaptation is the regulation of monovalent ion concentrations. Ion regulation determines many fundamental physiological parameters, such as cell volume, membrane potential, and intracellular pH. It is achieved through the concerted activities of multiple cellular components, including ion transporters and signaling molecules, on both short and long time scales. Although each component has been studied in detail previously, it remains unclear how the physiological parameters are maintained and regulated by the concerted action of all components under a diverse range of stress conditions. In this study, we have constructed an integrated mathematical model of ion regulation in Saccharomyces cerevisiae to understand this coordinated adaptation process. Using this model, we first predict that the interaction between phosphorylated Hog1p and Tok1p at the plasma membrane inhibits Tok1p activity and consequently reduces Na(+) influx under NaCl stress. We further characterize the impacts of NaCl, sorbitol, KCl and alkaline pH stresses on the cellular physiology and the differences between the cellular responses to these stresses. We predict that the calcineurin pathway is essential for maintaining a non-toxic level of intracellular Na(+) in the long-term adaptation to NaCl stress, but that its activation is not required for maintaining a low level of Na(+) under other stresses investigated. We provide evidence that, in addition to extrusion of toxic ions, Ena1p plays an important role, in some cases alongside Nha1p, in re-establishing membrane potential after stress perturbation. To conclude, this model serves as a powerful tool for both understanding the complex system-level properties of the highly coordinated adaptation process and generating further hypotheses for experimental investigation. Public Library of Science 2013-01-17 /pmc/articles/PMC3547829/ /pubmed/23341767 http://dx.doi.org/10.1371/journal.pcbi.1002879 Text en © 2013 Ke 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
Ke, Ruian
Ingram, Piers J.
Haynes, Ken
An Integrative Model of Ion Regulation in Yeast
title An Integrative Model of Ion Regulation in Yeast
title_full An Integrative Model of Ion Regulation in Yeast
title_fullStr An Integrative Model of Ion Regulation in Yeast
title_full_unstemmed An Integrative Model of Ion Regulation in Yeast
title_short An Integrative Model of Ion Regulation in Yeast
title_sort integrative model of ion regulation in yeast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547829/
https://www.ncbi.nlm.nih.gov/pubmed/23341767
http://dx.doi.org/10.1371/journal.pcbi.1002879
work_keys_str_mv AT keruian anintegrativemodelofionregulationinyeast
AT ingrampiersj anintegrativemodelofionregulationinyeast
AT haynesken anintegrativemodelofionregulationinyeast
AT keruian integrativemodelofionregulationinyeast
AT ingrampiersj integrativemodelofionregulationinyeast
AT haynesken integrativemodelofionregulationinyeast