| Literature DB >> 27129278 |
Lindsy R Boateng1, David Bennin2, Sofia De Oliveira2, Anna Huttenlocher3.
Abstract
Mammalian actin-binding protein-1 (mAbp1) is an adaptor protein that binds actin and modulates scission during endocytosis. Recent studies suggest that mAbp1 impairs cell invasion; however, the mechanism for the inhibitory effects of mAbp1 remain unclear. We performed a yeast two-hybrid screen and identified the adaptor protein, FHL2, as a novel binding partner that interacts with the N-terminal actin depolymerizing factor homology domain (ADFH) domain of mAbp1. Here we report that depletion of mAbp1 or ectopic expression of the ADFH domain of mAbp1 increased Rho GTPase signaling and breast cancer cell invasion. Moreover, cell invasion induced by the ADFH domain of mAbp1 required the expression of FHL2. Taken together, our findings show that mAbp1 and FHL2 are novel binding partners that differentially regulate Rho GTPase signaling and MTLn3 breast cancer cell invasion.Entities:
Keywords: FHL2; Rho (Rho GTPase); adaptor protein; cell invasion; cell migration; focal adhesion; mAbp1
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Year: 2016 PMID: 27129278 PMCID: PMC4933159 DOI: 10.1074/jbc.M116.725739
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157