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From graph topology to ODE models for gene regulatory networks

A gene regulatory network can be described at a high level by a directed graph with signed edges, and at a more detailed level by a system of ordinary differential equations (ODEs). The former qualitatively models the causal regulatory interactions between ordered pairs of genes, while the latter qu...

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Detalles Bibliográficos
Autores principales: Kang, Xiaohan, Hajek, Bruce, Hanzawa, Yoshie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326199/
https://www.ncbi.nlm.nih.gov/pubmed/32603340
http://dx.doi.org/10.1371/journal.pone.0235070
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author Kang, Xiaohan
Hajek, Bruce
Hanzawa, Yoshie
author_facet Kang, Xiaohan
Hajek, Bruce
Hanzawa, Yoshie
author_sort Kang, Xiaohan
collection PubMed
description A gene regulatory network can be described at a high level by a directed graph with signed edges, and at a more detailed level by a system of ordinary differential equations (ODEs). The former qualitatively models the causal regulatory interactions between ordered pairs of genes, while the latter quantitatively models the time-varying concentrations of mRNA and proteins. This paper clarifies the connection between the two types of models. We propose a property, called the constant sign property, for a general class of ODE models. The constant sign property characterizes the set of conditions (system parameters, external signals, or internal states) under which an ODE model is consistent with a signed, directed graph. If the constant sign property for an ODE model holds globally for all conditions, then the ODE model has a single signed, directed graph. If the constant sign property for an ODE model only holds locally, which may be more typical, then the ODE model corresponds to different graphs under different sets of conditions. In addition, two versions of constant sign property are given and a relationship between them is proved. As an example, the ODE models that capture the effect of cis-regulatory elements involving protein complex binding, based on the model in the GeneNetWeaver source code, are described in detail and shown to satisfy the global constant sign property with a unique consistent gene regulatory graph. Even a single gene regulatory graph is shown to have many ODE models of GeneNetWeaver type consistent with it due to combinatorial complexity and continuous parameters. Finally the question of how closely data generated by one ODE model can be fit by another ODE model is explored. It is observed that the fit is better if the two models come from the same graph.
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spelling pubmed-73261992020-07-10 From graph topology to ODE models for gene regulatory networks Kang, Xiaohan Hajek, Bruce Hanzawa, Yoshie PLoS One Research Article A gene regulatory network can be described at a high level by a directed graph with signed edges, and at a more detailed level by a system of ordinary differential equations (ODEs). The former qualitatively models the causal regulatory interactions between ordered pairs of genes, while the latter quantitatively models the time-varying concentrations of mRNA and proteins. This paper clarifies the connection between the two types of models. We propose a property, called the constant sign property, for a general class of ODE models. The constant sign property characterizes the set of conditions (system parameters, external signals, or internal states) under which an ODE model is consistent with a signed, directed graph. If the constant sign property for an ODE model holds globally for all conditions, then the ODE model has a single signed, directed graph. If the constant sign property for an ODE model only holds locally, which may be more typical, then the ODE model corresponds to different graphs under different sets of conditions. In addition, two versions of constant sign property are given and a relationship between them is proved. As an example, the ODE models that capture the effect of cis-regulatory elements involving protein complex binding, based on the model in the GeneNetWeaver source code, are described in detail and shown to satisfy the global constant sign property with a unique consistent gene regulatory graph. Even a single gene regulatory graph is shown to have many ODE models of GeneNetWeaver type consistent with it due to combinatorial complexity and continuous parameters. Finally the question of how closely data generated by one ODE model can be fit by another ODE model is explored. It is observed that the fit is better if the two models come from the same graph. Public Library of Science 2020-06-30 /pmc/articles/PMC7326199/ /pubmed/32603340 http://dx.doi.org/10.1371/journal.pone.0235070 Text en © 2020 Kang 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kang, Xiaohan
Hajek, Bruce
Hanzawa, Yoshie
From graph topology to ODE models for gene regulatory networks
title From graph topology to ODE models for gene regulatory networks
title_full From graph topology to ODE models for gene regulatory networks
title_fullStr From graph topology to ODE models for gene regulatory networks
title_full_unstemmed From graph topology to ODE models for gene regulatory networks
title_short From graph topology to ODE models for gene regulatory networks
title_sort from graph topology to ode models for gene regulatory networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326199/
https://www.ncbi.nlm.nih.gov/pubmed/32603340
http://dx.doi.org/10.1371/journal.pone.0235070
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