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Evolving Sensitivity Balances Boolean Networks

We investigate the sensitivity of Boolean Networks (BNs) to mutations. We are interested in Boolean Networks as a model of Gene Regulatory Networks (GRNs). We adopt Ribeiro and Kauffman’s Ergodic Set and use it to study the long term dynamics of a BN. We define the sensitivity of a BN to be the mean...

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Autores principales: Luo, Jamie X., Turner, Matthew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346810/
https://www.ncbi.nlm.nih.gov/pubmed/22586459
http://dx.doi.org/10.1371/journal.pone.0036010
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author Luo, Jamie X.
Turner, Matthew S.
author_facet Luo, Jamie X.
Turner, Matthew S.
author_sort Luo, Jamie X.
collection PubMed
description We investigate the sensitivity of Boolean Networks (BNs) to mutations. We are interested in Boolean Networks as a model of Gene Regulatory Networks (GRNs). We adopt Ribeiro and Kauffman’s Ergodic Set and use it to study the long term dynamics of a BN. We define the sensitivity of a BN to be the mean change in its Ergodic Set structure under all possible loss of interaction mutations. Insilico experiments were used to selectively evolve BNs for sensitivity to losing interactions. We find that maximum sensitivity was often achievable and resulted in the BNs becoming topologically balanced, i.e. they evolve towards network structures in which they have a similar number of inhibitory and excitatory interactions. In terms of the dynamics, the dominant sensitivity strategy that evolved was to build BNs with Ergodic Sets dominated by a single long limit cycle which is easily destabilised by mutations. We discuss the relevance of our findings in the context of Stem Cell Differentiation and propose a relationship between pluripotent stem cells and our evolved sensitive networks.
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spelling pubmed-33468102012-05-14 Evolving Sensitivity Balances Boolean Networks Luo, Jamie X. Turner, Matthew S. PLoS One Research Article We investigate the sensitivity of Boolean Networks (BNs) to mutations. We are interested in Boolean Networks as a model of Gene Regulatory Networks (GRNs). We adopt Ribeiro and Kauffman’s Ergodic Set and use it to study the long term dynamics of a BN. We define the sensitivity of a BN to be the mean change in its Ergodic Set structure under all possible loss of interaction mutations. Insilico experiments were used to selectively evolve BNs for sensitivity to losing interactions. We find that maximum sensitivity was often achievable and resulted in the BNs becoming topologically balanced, i.e. they evolve towards network structures in which they have a similar number of inhibitory and excitatory interactions. In terms of the dynamics, the dominant sensitivity strategy that evolved was to build BNs with Ergodic Sets dominated by a single long limit cycle which is easily destabilised by mutations. We discuss the relevance of our findings in the context of Stem Cell Differentiation and propose a relationship between pluripotent stem cells and our evolved sensitive networks. Public Library of Science 2012-05-07 /pmc/articles/PMC3346810/ /pubmed/22586459 http://dx.doi.org/10.1371/journal.pone.0036010 Text en Luo, Turner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Luo, Jamie X.
Turner, Matthew S.
Evolving Sensitivity Balances Boolean Networks
title Evolving Sensitivity Balances Boolean Networks
title_full Evolving Sensitivity Balances Boolean Networks
title_fullStr Evolving Sensitivity Balances Boolean Networks
title_full_unstemmed Evolving Sensitivity Balances Boolean Networks
title_short Evolving Sensitivity Balances Boolean Networks
title_sort evolving sensitivity balances boolean networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346810/
https://www.ncbi.nlm.nih.gov/pubmed/22586459
http://dx.doi.org/10.1371/journal.pone.0036010
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