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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-5916526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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