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Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human

BACKGROUND: Gene regulatory networks are complex dynamic systems and the reverse-engineering of such networks from high-dimensional time course transcriptomic data have attracted researchers from various fields. It is also interesting and important to study the behavior of the reconstructed networks...

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Autores principales: Sun, Xiaodian, Hu, Fang, Wu, Shuang, Qiu, Xing, Linel, Patrice, Wu, Hulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963324/
https://www.ncbi.nlm.nih.gov/pubmed/29928721
http://dx.doi.org/10.1016/j.idm.2016.07.002
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author Sun, Xiaodian
Hu, Fang
Wu, Shuang
Qiu, Xing
Linel, Patrice
Wu, Hulin
author_facet Sun, Xiaodian
Hu, Fang
Wu, Shuang
Qiu, Xing
Linel, Patrice
Wu, Hulin
author_sort Sun, Xiaodian
collection PubMed
description BACKGROUND: Gene regulatory networks are complex dynamic systems and the reverse-engineering of such networks from high-dimensional time course transcriptomic data have attracted researchers from various fields. It is also interesting and important to study the behavior of the reconstructed networks on the basis of dynamic models and the biological mechanisms. We focus on the gene regulatory networks reconstructed using the ordinary differential equation (ODE) modelling approach and investigate the properties of these networks. RESULTS: Controllability and stability analyses are conducted for the reconstructed gene response networks of 17 influenza infected subjects based on ODE models. Symptomatic subjects tend to have larger numbers of driver nodes, higher proportions of critical links and lower proportions of redundant links than asymptomatic subjects. We also show that the degree distribution, rather than the structure of networks, plays an important role in controlling the network in response to influenza infection. In addition, we find that the stability of high-dimensional networks is very sensitive to randomness in the reconstructed systems brought by errors in measurements and parameter estimation. CONCLUSIONS: The gene response networks of asymptomatic subjects are easier to be controlled than those of symptomatic subjects. This may indicate that the regulatory systems of asymptomatic subjects are easier to recover from disease stimulations, so these subjects are less likely to develop symptoms. Our results also suggest that stability constraint should be considered in the modelling of high-dimensional networks and the estimation of network parameters.
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spelling pubmed-59633242018-06-20 Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human Sun, Xiaodian Hu, Fang Wu, Shuang Qiu, Xing Linel, Patrice Wu, Hulin Infect Dis Model Article BACKGROUND: Gene regulatory networks are complex dynamic systems and the reverse-engineering of such networks from high-dimensional time course transcriptomic data have attracted researchers from various fields. It is also interesting and important to study the behavior of the reconstructed networks on the basis of dynamic models and the biological mechanisms. We focus on the gene regulatory networks reconstructed using the ordinary differential equation (ODE) modelling approach and investigate the properties of these networks. RESULTS: Controllability and stability analyses are conducted for the reconstructed gene response networks of 17 influenza infected subjects based on ODE models. Symptomatic subjects tend to have larger numbers of driver nodes, higher proportions of critical links and lower proportions of redundant links than asymptomatic subjects. We also show that the degree distribution, rather than the structure of networks, plays an important role in controlling the network in response to influenza infection. In addition, we find that the stability of high-dimensional networks is very sensitive to randomness in the reconstructed systems brought by errors in measurements and parameter estimation. CONCLUSIONS: The gene response networks of asymptomatic subjects are easier to be controlled than those of symptomatic subjects. This may indicate that the regulatory systems of asymptomatic subjects are easier to recover from disease stimulations, so these subjects are less likely to develop symptoms. Our results also suggest that stability constraint should be considered in the modelling of high-dimensional networks and the estimation of network parameters. KeAi Publishing 2016-09-13 /pmc/articles/PMC5963324/ /pubmed/29928721 http://dx.doi.org/10.1016/j.idm.2016.07.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sun, Xiaodian
Hu, Fang
Wu, Shuang
Qiu, Xing
Linel, Patrice
Wu, Hulin
Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title_full Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title_fullStr Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title_full_unstemmed Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title_short Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
title_sort controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963324/
https://www.ncbi.nlm.nih.gov/pubmed/29928721
http://dx.doi.org/10.1016/j.idm.2016.07.002
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