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Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast

The high osmolarity glycerol (HOG) pathway in yeast serves as a prototype signalling system for eukaryotes. We used an unprecedented amount of data to parameterise 192 models capturing different hypotheses about molecular mechanisms underlying osmo-adaptation and selected a best approximating model....

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Autores principales: Schaber, Jörg, Baltanas, Rodrigo, Bush, Alan, Klipp, Edda, Colman-Lerner, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531907/
https://www.ncbi.nlm.nih.gov/pubmed/23149687
http://dx.doi.org/10.1038/msb.2012.53
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author Schaber, Jörg
Baltanas, Rodrigo
Bush, Alan
Klipp, Edda
Colman-Lerner, Alejandro
author_facet Schaber, Jörg
Baltanas, Rodrigo
Bush, Alan
Klipp, Edda
Colman-Lerner, Alejandro
author_sort Schaber, Jörg
collection PubMed
description The high osmolarity glycerol (HOG) pathway in yeast serves as a prototype signalling system for eukaryotes. We used an unprecedented amount of data to parameterise 192 models capturing different hypotheses about molecular mechanisms underlying osmo-adaptation and selected a best approximating model. This model implied novel mechanisms regulating osmo-adaptation in yeast. The model suggested that (i) the main mechanism for osmo-adaptation is a fast and transient non-transcriptional Hog1-mediated activation of glycerol production, (ii) the transcriptional response serves to maintain an increased steady-state glycerol production with low steady-state Hog1 activity, and (iii) fast negative feedbacks of activated Hog1 on upstream signalling branches serves to stabilise adaptation response. The best approximating model also indicated that homoeostatic adaptive systems with two parallel redundant signalling branches show a more robust and faster response than single-branch systems. We corroborated this notion to a large extent by dedicated measurements of volume recovery in single cells. Our study also demonstrates that systematically testing a model ensemble against data has the potential to achieve a better and unbiased understanding of molecular mechanisms.
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spelling pubmed-35319072012-12-28 Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast Schaber, Jörg Baltanas, Rodrigo Bush, Alan Klipp, Edda Colman-Lerner, Alejandro Mol Syst Biol Article The high osmolarity glycerol (HOG) pathway in yeast serves as a prototype signalling system for eukaryotes. We used an unprecedented amount of data to parameterise 192 models capturing different hypotheses about molecular mechanisms underlying osmo-adaptation and selected a best approximating model. This model implied novel mechanisms regulating osmo-adaptation in yeast. The model suggested that (i) the main mechanism for osmo-adaptation is a fast and transient non-transcriptional Hog1-mediated activation of glycerol production, (ii) the transcriptional response serves to maintain an increased steady-state glycerol production with low steady-state Hog1 activity, and (iii) fast negative feedbacks of activated Hog1 on upstream signalling branches serves to stabilise adaptation response. The best approximating model also indicated that homoeostatic adaptive systems with two parallel redundant signalling branches show a more robust and faster response than single-branch systems. We corroborated this notion to a large extent by dedicated measurements of volume recovery in single cells. Our study also demonstrates that systematically testing a model ensemble against data has the potential to achieve a better and unbiased understanding of molecular mechanisms. European Molecular Biology Organization 2012-11-13 /pmc/articles/PMC3531907/ /pubmed/23149687 http://dx.doi.org/10.1038/msb.2012.53 Text en Copyright © 2012, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Article
Schaber, Jörg
Baltanas, Rodrigo
Bush, Alan
Klipp, Edda
Colman-Lerner, Alejandro
Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title_full Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title_fullStr Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title_full_unstemmed Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title_short Modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
title_sort modelling reveals novel roles of two parallel signalling pathways and homeostatic feedbacks in yeast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531907/
https://www.ncbi.nlm.nih.gov/pubmed/23149687
http://dx.doi.org/10.1038/msb.2012.53
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