Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783552301466648576 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7326199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kangxiaohan fromgraphtopologytoodemodelsforgeneregulatorynetworks AT hajekbruce fromgraphtopologytoodemodelsforgeneregulatorynetworks AT hanzawayoshie fromgraphtopologytoodemodelsforgeneregulatorynetworks |