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Automated Ensemble Modeling with modelMaGe: Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG Pathway
In systems biology uncertainty about biological processes translates into alternative mathematical model candidates. Here, the goal is to generate, fit and discriminate several candidate models that represent different hypotheses for feedback mechanisms responsible for downregulating the response of...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068199/ https://www.ncbi.nlm.nih.gov/pubmed/21483474 http://dx.doi.org/10.1371/journal.pone.0014791 |
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author | Schaber, Jörg Flöttmann, Max Li, Jian Tiger, Carl-Fredrik Hohmann, Stefan Klipp, Edda |
author_facet | Schaber, Jörg Flöttmann, Max Li, Jian Tiger, Carl-Fredrik Hohmann, Stefan Klipp, Edda |
author_sort | Schaber, Jörg |
collection | PubMed |
description | In systems biology uncertainty about biological processes translates into alternative mathematical model candidates. Here, the goal is to generate, fit and discriminate several candidate models that represent different hypotheses for feedback mechanisms responsible for downregulating the response of the Sho1 branch of the yeast high osmolarity glycerol (HOG) signaling pathway after initial stimulation. Implementing and testing these candidate models by hand is a tedious and error-prone task. Therefore, we automatically generated a set of candidate models of the Sho1 branch with the tool modelMaGe. These candidate models are automatically documented, can readily be simulated and fitted automatically to data. A ranking of the models with respect to parsimonious data representation is provided, enabling discrimination between candidate models and the biological hypotheses underlying them. We conclude that a previously published model fitted spurious effects in the data. Moreover, the discrimination analysis suggests that the reported data does not support the conclusion that a desensitization mechanism leads to the rapid attenuation of Hog1 signaling in the Sho1 branch of the HOG pathway. The data rather supports a model where an integrator feedback shuts down the pathway. This conclusion is also supported by dedicated experiments that can exclusively be predicted by those models including an integrator feedback. modelMaGe is an open source project and is distributed under the Gnu General Public License (GPL) and is available from http://modelmage.org. |
format | Text |
id | pubmed-3068199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30681992011-04-11 Automated Ensemble Modeling with modelMaGe: Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG Pathway Schaber, Jörg Flöttmann, Max Li, Jian Tiger, Carl-Fredrik Hohmann, Stefan Klipp, Edda PLoS One Research Article In systems biology uncertainty about biological processes translates into alternative mathematical model candidates. Here, the goal is to generate, fit and discriminate several candidate models that represent different hypotheses for feedback mechanisms responsible for downregulating the response of the Sho1 branch of the yeast high osmolarity glycerol (HOG) signaling pathway after initial stimulation. Implementing and testing these candidate models by hand is a tedious and error-prone task. Therefore, we automatically generated a set of candidate models of the Sho1 branch with the tool modelMaGe. These candidate models are automatically documented, can readily be simulated and fitted automatically to data. A ranking of the models with respect to parsimonious data representation is provided, enabling discrimination between candidate models and the biological hypotheses underlying them. We conclude that a previously published model fitted spurious effects in the data. Moreover, the discrimination analysis suggests that the reported data does not support the conclusion that a desensitization mechanism leads to the rapid attenuation of Hog1 signaling in the Sho1 branch of the HOG pathway. The data rather supports a model where an integrator feedback shuts down the pathway. This conclusion is also supported by dedicated experiments that can exclusively be predicted by those models including an integrator feedback. modelMaGe is an open source project and is distributed under the Gnu General Public License (GPL) and is available from http://modelmage.org. Public Library of Science 2011-03-30 /pmc/articles/PMC3068199/ /pubmed/21483474 http://dx.doi.org/10.1371/journal.pone.0014791 Text en Schaber 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 Schaber, Jörg Flöttmann, Max Li, Jian Tiger, Carl-Fredrik Hohmann, Stefan Klipp, Edda Automated Ensemble Modeling with modelMaGe: Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG Pathway |
title | Automated Ensemble Modeling with modelMaGe:
Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG
Pathway |
title_full | Automated Ensemble Modeling with modelMaGe:
Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG
Pathway |
title_fullStr | Automated Ensemble Modeling with modelMaGe:
Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG
Pathway |
title_full_unstemmed | Automated Ensemble Modeling with modelMaGe:
Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG
Pathway |
title_short | Automated Ensemble Modeling with modelMaGe:
Analyzing Feedback Mechanisms in the Sho1 Branch of the HOG
Pathway |
title_sort | automated ensemble modeling with modelmage:
analyzing feedback mechanisms in the sho1 branch of the hog
pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068199/ https://www.ncbi.nlm.nih.gov/pubmed/21483474 http://dx.doi.org/10.1371/journal.pone.0014791 |
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