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Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation
The Rac1 GTPase plays key roles in cytoskeletal organization, cell motility and a variety of physiological and disease-linked responses. Wild type Rac1 signaling entails dissociation of the GTPase from cytosolic Rac1-Rho GDP dissociation inhibitor (GDI) complexes, translocation to membranes, activat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105943/ https://www.ncbi.nlm.nih.gov/pubmed/27835684 http://dx.doi.org/10.1371/journal.pone.0166715 |
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author | Castro-Castro, Antonio Muriel, Olivia del Pozo, Miguel A. Bustelo, Xosé R. |
author_facet | Castro-Castro, Antonio Muriel, Olivia del Pozo, Miguel A. Bustelo, Xosé R. |
author_sort | Castro-Castro, Antonio |
collection | PubMed |
description | The Rac1 GTPase plays key roles in cytoskeletal organization, cell motility and a variety of physiological and disease-linked responses. Wild type Rac1 signaling entails dissociation of the GTPase from cytosolic Rac1-Rho GDP dissociation inhibitor (GDI) complexes, translocation to membranes, activation by exchange factors, effector binding, and activation of downstream signaling cascades. Out of those steps, membrane translocation is the less understood. Using transfections of a expression cDNA library in cells expressing a Rac1 bioreporter, we previously identified a cytoskeletal feedback loop nucleated by the F-actin binding protein coronin 1A (Coro1A) that promotes Rac1 translocation to the plasma membrane by facilitating the Pak-dependent dissociation of Rac1-Rho GDI complexes. This screening identified other potential regulators of this process, including WDR26, basigin, and TMEM8A. Here, we show that WDR26 promotes Rac1 translocation following a Coro1A-like and Coro1A-dependent mechanism. By contrast, basigin and TMEM8A stabilize Rac1 at the plasma membrane by inhibiting the internalization of caveolin-rich membrane subdomains. This latter pathway is F-actin-dependent but Coro1A-, Pak- and Rho GDI-independent. |
format | Online Article Text |
id | pubmed-5105943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51059432016-12-08 Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation Castro-Castro, Antonio Muriel, Olivia del Pozo, Miguel A. Bustelo, Xosé R. PLoS One Research Article The Rac1 GTPase plays key roles in cytoskeletal organization, cell motility and a variety of physiological and disease-linked responses. Wild type Rac1 signaling entails dissociation of the GTPase from cytosolic Rac1-Rho GDP dissociation inhibitor (GDI) complexes, translocation to membranes, activation by exchange factors, effector binding, and activation of downstream signaling cascades. Out of those steps, membrane translocation is the less understood. Using transfections of a expression cDNA library in cells expressing a Rac1 bioreporter, we previously identified a cytoskeletal feedback loop nucleated by the F-actin binding protein coronin 1A (Coro1A) that promotes Rac1 translocation to the plasma membrane by facilitating the Pak-dependent dissociation of Rac1-Rho GDI complexes. This screening identified other potential regulators of this process, including WDR26, basigin, and TMEM8A. Here, we show that WDR26 promotes Rac1 translocation following a Coro1A-like and Coro1A-dependent mechanism. By contrast, basigin and TMEM8A stabilize Rac1 at the plasma membrane by inhibiting the internalization of caveolin-rich membrane subdomains. This latter pathway is F-actin-dependent but Coro1A-, Pak- and Rho GDI-independent. Public Library of Science 2016-11-11 /pmc/articles/PMC5105943/ /pubmed/27835684 http://dx.doi.org/10.1371/journal.pone.0166715 Text en © 2016 Castro-Castro 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 Castro-Castro, Antonio Muriel, Olivia del Pozo, Miguel A. Bustelo, Xosé R. Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title | Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title_full | Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title_fullStr | Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title_full_unstemmed | Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title_short | Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation |
title_sort | characterization of novel molecular mechanisms favoring rac1 membrane translocation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105943/ https://www.ncbi.nlm.nih.gov/pubmed/27835684 http://dx.doi.org/10.1371/journal.pone.0166715 |
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