Coronin 1A promotes a cytoskeletal-based feedback loop that facilitates Rac1 translocation and activation.

Antonio Castro-Castro, Virginia Ojeda, María Barreira, Vincent Sauzeau, Inmaculada Navarro-Lérida, Olivia Muriel, José R Couceiro, Felipe X Pimentel-Muíños, Miguel A Del Pozo, Xosé R Bustelo

文献索引：EMBO J. 30 , 3913-3927, (2011)

全文：HTML全文

摘要

The activation of the Rac1 GTPase during cell signalling entails its translocation from the cytosol to membranes, release from sequestering Rho GDP dissociation inhibitors (RhoGDI), and GDP/GTP exchange. In addition to those steps, we show here that optimal Rac1 activation during cell signalling requires the engagement of a downstream, cytoskeletal-based feedback loop nucleated around the cytoskeletal protein coronin 1A and the Rac1 exchange factor ArhGEF7. These two proteins form a cytosolic complex that, upon Rac1-driven F-actin polymerization, translocates to juxtamembrane areas where it expands the pool of activated, membrane-bound Rac1. Such activity requires the formation of an F-actin/ArhGEF7-dependent physical complex of coronin 1A with Pak1 and RhoGDIα that, once assembled, promotes the Pak1-dependent dissociation of Rac1 from the Rac1/RhoGDIα complex and subsequent Rac1 activation. Genetic evidence demonstrates that this relay circuit is essential for generating sustained Rac1 activation levels during cell signalling.