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dc.contributor.authorCastro-Castro, Antonio
dc.contributor.authorMuriel, Olivia 
dc.contributor.authordel Pozo, Miguel Angel 
dc.contributor.authorBustelo, Xose R.
dc.date.accessioned2017-10-20T10:33:51Z
dc.date.available2017-10-20T10:33:51Z
dc.date.issued2016
dc.identifierISI:000387779200065
dc.identifier.citationPLoS One. 2016; 11(11):e0166715
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/20.500.12105/5177
dc.description.abstractThe 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.
dc.description.sponsorshipXRB has been supported by grants from the Spanish Ministry of Economy and Competitiveness (RD12/0036/0002, SAF2015-64556-R), Worldwide Cancer Research (14-1248), Ramon Areces Foundation, Consejeria de Educacion of the Junta de Castilla y Leon (CSI049U16), and Fundacion Cientifica Asociacion Espanola contra el Cancer (GD16173472GARC). Funding from both the Spanish Ministry of Economy and Competitiveness and Junta de Castilla y Leon is partially contributed by the European Regional Development Fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
dc.language.isoeng
dc.publisherPUBLIC LIBRARY SCIENCE
dc.relation.isversionofPublisher's version
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectINTEGRIN-ASSOCIATED PROTEIN
dc.subjectSMALL GTPASE RAC
dc.subjectG-BETA-GAMMA
dc.subjectCELL-MIGRATION
dc.subjectPLASMA-MEMBRANE
dc.subjectCORONIN 1A
dc.subjectSIGNAL-TRANSDUCTION
dc.subjectLIPID RAFTS
dc.subjectACTIVATION
dc.subjectDISSOCIATION
dc.titleCharacterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation
dc.typeArtículo
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID27835684
dc.format.volume11
dc.identifier.doi10.1371/journal.pone.0166715
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderWorldwide Cancer Research
dc.contributor.funderFundación Ramón Areces
dc.contributor.funderAsociación Española Contra el Cáncer
dc.contributor.funderJunta de Castilla y León (España)
dc.description.peerreviewed
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0166715
dc.identifier.journalPLoS One
dc.repisalud.orgCNICCNIC::Grupos de investigación::Señalización por Integrinas
dc.repisalud.institucionCNIC
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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