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Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis

BACKGROUND: Inverse modelling of gene regulatory networks (GRNs) capable of simulating continuous spatio-temporal biological processes requires accurate data and a good description of the system. If quantitative relations between genes cannot be extracted from direct measurements, an efficient metho...

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Autores principales: Fomekong-Nanfack, Yves, Postma, Marten, Kaandorp, Jaap A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761871/
https://www.ncbi.nlm.nih.gov/pubmed/19769791
http://dx.doi.org/10.1186/1752-0509-3-94
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author Fomekong-Nanfack, Yves
Postma, Marten
Kaandorp, Jaap A
author_facet Fomekong-Nanfack, Yves
Postma, Marten
Kaandorp, Jaap A
author_sort Fomekong-Nanfack, Yves
collection PubMed
description BACKGROUND: Inverse modelling of gene regulatory networks (GRNs) capable of simulating continuous spatio-temporal biological processes requires accurate data and a good description of the system. If quantitative relations between genes cannot be extracted from direct measurements, an efficient method to estimate the unknown parameters is mandatory. A model that has been proposed to simulate spatio-temporal gene expression patterns is the connectionist model. This method describes the quantitative dynamics of a regulatory network in space. The model parameters are estimated by means of model-fitting algorithms. The gene interactions are identified without making any prior assumptions concerning the network connectivity. As a result, the inverse modelling might lead to multiple circuits showing the same quantitative behaviour and it is not possible to identify one optimal circuit. Consequently, it is important to address the quality of the circuits in terms of model robustness. RESULTS: Here we investigate the sensitivity and robustness of circuits obtained from reverse engineering a model capable of simulating measured gene expression patterns. As a case study we use the early gap gene segmentation mechanism in Drosophila melanogaster. We consider the limitations of the connectionist model used to describe GRN Inferred from spatio-temporal gene expression. We address the problem of circuit discrimination, where the selection criterion within the optimization technique is based of the least square minimization on the error between data and simulated results. CONCLUSION: Parameter sensitivity analysis allows one to discriminate between circuits having significant parameter and qualitative differences but exhibiting the same quantitative pattern. Furthermore, we show that using a stochastic model derived from a deterministic solution, one can introduce fluctuations within the model to analyze the circuits' robustness. Ultimately, we show that there is a close relation between circuit sensitivity and robustness to fluctuation, and that circuit robustness is rather modular than global. The current study shows that reverse engineering of GRNs should not only focus on estimating parameters by minimizing the difference between observation and simulation but also on other model properties. Our study suggests that multi-objective optimization based on robustness and sensitivity analysis has to be considered.
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spelling pubmed-27618712009-10-15 Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis Fomekong-Nanfack, Yves Postma, Marten Kaandorp, Jaap A BMC Syst Biol Research Article BACKGROUND: Inverse modelling of gene regulatory networks (GRNs) capable of simulating continuous spatio-temporal biological processes requires accurate data and a good description of the system. If quantitative relations between genes cannot be extracted from direct measurements, an efficient method to estimate the unknown parameters is mandatory. A model that has been proposed to simulate spatio-temporal gene expression patterns is the connectionist model. This method describes the quantitative dynamics of a regulatory network in space. The model parameters are estimated by means of model-fitting algorithms. The gene interactions are identified without making any prior assumptions concerning the network connectivity. As a result, the inverse modelling might lead to multiple circuits showing the same quantitative behaviour and it is not possible to identify one optimal circuit. Consequently, it is important to address the quality of the circuits in terms of model robustness. RESULTS: Here we investigate the sensitivity and robustness of circuits obtained from reverse engineering a model capable of simulating measured gene expression patterns. As a case study we use the early gap gene segmentation mechanism in Drosophila melanogaster. We consider the limitations of the connectionist model used to describe GRN Inferred from spatio-temporal gene expression. We address the problem of circuit discrimination, where the selection criterion within the optimization technique is based of the least square minimization on the error between data and simulated results. CONCLUSION: Parameter sensitivity analysis allows one to discriminate between circuits having significant parameter and qualitative differences but exhibiting the same quantitative pattern. Furthermore, we show that using a stochastic model derived from a deterministic solution, one can introduce fluctuations within the model to analyze the circuits' robustness. Ultimately, we show that there is a close relation between circuit sensitivity and robustness to fluctuation, and that circuit robustness is rather modular than global. The current study shows that reverse engineering of GRNs should not only focus on estimating parameters by minimizing the difference between observation and simulation but also on other model properties. Our study suggests that multi-objective optimization based on robustness and sensitivity analysis has to be considered. BioMed Central 2009-09-21 /pmc/articles/PMC2761871/ /pubmed/19769791 http://dx.doi.org/10.1186/1752-0509-3-94 Text en Copyright © 2009 Fomekong-Nanfack 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
Fomekong-Nanfack, Yves
Postma, Marten
Kaandorp, Jaap A
Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title_full Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title_fullStr Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title_full_unstemmed Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title_short Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
title_sort inferring drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761871/
https://www.ncbi.nlm.nih.gov/pubmed/19769791
http://dx.doi.org/10.1186/1752-0509-3-94
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