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Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle

BACKGROUND: One of the most well described cellular processes is the cell cycle, governing cell division. Mathematical models of this gene-protein network are therefore a good test case for assessing to what extent we can dissect the relationship between model parameters and system dynamics. Here we...

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Autores principales: Eriksson, Olivia, Andersson, Tom, Zhou, Yishao, Tegnér, Jesper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176200/
https://www.ncbi.nlm.nih.gov/pubmed/21819620
http://dx.doi.org/10.1186/1752-0509-5-123
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author Eriksson, Olivia
Andersson, Tom
Zhou, Yishao
Tegnér, Jesper
author_facet Eriksson, Olivia
Andersson, Tom
Zhou, Yishao
Tegnér, Jesper
author_sort Eriksson, Olivia
collection PubMed
description BACKGROUND: One of the most well described cellular processes is the cell cycle, governing cell division. Mathematical models of this gene-protein network are therefore a good test case for assessing to what extent we can dissect the relationship between model parameters and system dynamics. Here we combine two strategies to enable an exploration of parameter space in relation to model output. A simplified, piecewise linear approximation of the original model is combined with a sensitivity analysis of the same system, to obtain and validate analytical expressions describing the dynamical role of different model parameters. RESULTS: We considered two different output responses to parameter perturbations. One was qualitative and described whether the system was still working, i.e. whether there were oscillations. We call parameters that correspond to such qualitative change in system response essential. The other response pattern was quantitative and measured changes in cell size, corresponding to perturbations of modulatory parameters. Analytical predictions from the simplified model concerning the impact of different parameters were compared to a sensitivity analysis of the original model, thus evaluating the predictions from the simplified model. The comparison showed that the predictions on essential and modulatory parameters were satisfactory for small perturbations, but more discrepancies were seen for larger perturbations. Furthermore, for this particular cell cycle model, we found that most parameters were either essential or modulatory. Essential parameters required large perturbations for identification, whereas modulatory parameters were more easily identified with small perturbations. Finally, we used the simplified model to make predictions on critical combinations of parameter perturbations. CONCLUSIONS: The parameter characterizations of the simplified model are in large consistent with the original model and the simplified model can give predictions on critical combinations of parameter perturbations. We believe that the distinction between essential and modulatory perturbation responses will be of use for sensitivity analysis, and in discussions of robustness and during the model simplification process.
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spelling pubmed-31762002011-09-20 Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle Eriksson, Olivia Andersson, Tom Zhou, Yishao Tegnér, Jesper BMC Syst Biol Research Article BACKGROUND: One of the most well described cellular processes is the cell cycle, governing cell division. Mathematical models of this gene-protein network are therefore a good test case for assessing to what extent we can dissect the relationship between model parameters and system dynamics. Here we combine two strategies to enable an exploration of parameter space in relation to model output. A simplified, piecewise linear approximation of the original model is combined with a sensitivity analysis of the same system, to obtain and validate analytical expressions describing the dynamical role of different model parameters. RESULTS: We considered two different output responses to parameter perturbations. One was qualitative and described whether the system was still working, i.e. whether there were oscillations. We call parameters that correspond to such qualitative change in system response essential. The other response pattern was quantitative and measured changes in cell size, corresponding to perturbations of modulatory parameters. Analytical predictions from the simplified model concerning the impact of different parameters were compared to a sensitivity analysis of the original model, thus evaluating the predictions from the simplified model. The comparison showed that the predictions on essential and modulatory parameters were satisfactory for small perturbations, but more discrepancies were seen for larger perturbations. Furthermore, for this particular cell cycle model, we found that most parameters were either essential or modulatory. Essential parameters required large perturbations for identification, whereas modulatory parameters were more easily identified with small perturbations. Finally, we used the simplified model to make predictions on critical combinations of parameter perturbations. CONCLUSIONS: The parameter characterizations of the simplified model are in large consistent with the original model and the simplified model can give predictions on critical combinations of parameter perturbations. We believe that the distinction between essential and modulatory perturbation responses will be of use for sensitivity analysis, and in discussions of robustness and during the model simplification process. BioMed Central 2011-08-07 /pmc/articles/PMC3176200/ /pubmed/21819620 http://dx.doi.org/10.1186/1752-0509-5-123 Text en Copyright ©2011 Eriksson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Eriksson, Olivia
Andersson, Tom
Zhou, Yishao
Tegnér, Jesper
Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title_full Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title_fullStr Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title_full_unstemmed Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title_short Decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
title_sort decoding complex biological networks - tracing essential and modulatory parameters in complex and simplified models of the cell cycle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176200/
https://www.ncbi.nlm.nih.gov/pubmed/21819620
http://dx.doi.org/10.1186/1752-0509-5-123
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