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Principles that govern competition or co-existence in Rho-GTPase driven polarization

Rho-GTPases are master regulators of polarity establishment and cell morphology. Positive feedback enables concentration of Rho-GTPases into clusters at the cell cortex, from where they regulate the cytoskeleton. Different cell types reproducibly generate either one (e.g. the front of a migrating ce...

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Autores principales: Chiou, Jian-Geng, Ramirez, Samuel A., Elston, Timothy C., Witelski, Thomas P., Schaeffer, David G., Lew, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916526/
https://www.ncbi.nlm.nih.gov/pubmed/29649212
http://dx.doi.org/10.1371/journal.pcbi.1006095
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author Chiou, Jian-Geng
Ramirez, Samuel A.
Elston, Timothy C.
Witelski, Thomas P.
Schaeffer, David G.
Lew, Daniel J.
author_facet Chiou, Jian-Geng
Ramirez, Samuel A.
Elston, Timothy C.
Witelski, Thomas P.
Schaeffer, David G.
Lew, Daniel J.
author_sort Chiou, Jian-Geng
collection PubMed
description Rho-GTPases are master regulators of polarity establishment and cell morphology. Positive feedback enables concentration of Rho-GTPases into clusters at the cell cortex, from where they regulate the cytoskeleton. Different cell types reproducibly generate either one (e.g. the front of a migrating cell) or several clusters (e.g. the multiple dendrites of a neuron), but the mechanistic basis for unipolar or multipolar outcomes is unclear. The design principles of Rho-GTPase circuits are captured by two-component reaction-diffusion models based on conserved aspects of Rho-GTPase biochemistry. Some such models display rapid winner-takes-all competition between clusters, yielding a unipolar outcome. Other models allow prolonged co-existence of clusters. We investigate the behavior of a simple class of models and show that while the timescale of competition varies enormously depending on model parameters, a single factor explains a large majority of this variation. The dominant factor concerns the degree to which the maximal active GTPase concentration in a cluster approaches a “saturation point” determined by model parameters. We suggest that both saturation and the effect of saturation on competition reflect fundamental properties of the Rho-GTPase polarity machinery, regardless of the specific feedback mechanism, which predict whether the system will generate unipolar or multipolar outcomes.
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spelling pubmed-59165262018-05-04 Principles that govern competition or co-existence in Rho-GTPase driven polarization Chiou, Jian-Geng Ramirez, Samuel A. Elston, Timothy C. Witelski, Thomas P. Schaeffer, David G. Lew, Daniel J. PLoS Comput Biol Research Article Rho-GTPases are master regulators of polarity establishment and cell morphology. Positive feedback enables concentration of Rho-GTPases into clusters at the cell cortex, from where they regulate the cytoskeleton. Different cell types reproducibly generate either one (e.g. the front of a migrating cell) or several clusters (e.g. the multiple dendrites of a neuron), but the mechanistic basis for unipolar or multipolar outcomes is unclear. The design principles of Rho-GTPase circuits are captured by two-component reaction-diffusion models based on conserved aspects of Rho-GTPase biochemistry. Some such models display rapid winner-takes-all competition between clusters, yielding a unipolar outcome. Other models allow prolonged co-existence of clusters. We investigate the behavior of a simple class of models and show that while the timescale of competition varies enormously depending on model parameters, a single factor explains a large majority of this variation. The dominant factor concerns the degree to which the maximal active GTPase concentration in a cluster approaches a “saturation point” determined by model parameters. We suggest that both saturation and the effect of saturation on competition reflect fundamental properties of the Rho-GTPase polarity machinery, regardless of the specific feedback mechanism, which predict whether the system will generate unipolar or multipolar outcomes. Public Library of Science 2018-04-12 /pmc/articles/PMC5916526/ /pubmed/29649212 http://dx.doi.org/10.1371/journal.pcbi.1006095 Text en © 2018 Chiou 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
Chiou, Jian-Geng
Ramirez, Samuel A.
Elston, Timothy C.
Witelski, Thomas P.
Schaeffer, David G.
Lew, Daniel J.
Principles that govern competition or co-existence in Rho-GTPase driven polarization
title Principles that govern competition or co-existence in Rho-GTPase driven polarization
title_full Principles that govern competition or co-existence in Rho-GTPase driven polarization
title_fullStr Principles that govern competition or co-existence in Rho-GTPase driven polarization
title_full_unstemmed Principles that govern competition or co-existence in Rho-GTPase driven polarization
title_short Principles that govern competition or co-existence in Rho-GTPase driven polarization
title_sort principles that govern competition or co-existence in rho-gtpase driven polarization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916526/
https://www.ncbi.nlm.nih.gov/pubmed/29649212
http://dx.doi.org/10.1371/journal.pcbi.1006095
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