Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoA

Authors: Prakash, Siddharth K.1; Paylor, Richard1; Jenna, Sarah2; Lamarche-Vane, Nathalie2; Armstrong, Dawna L.3; Xu, Bisong1; Mancini, Michael A.4; Zoghbi, Huda Y.1

Source: Human Molecular Genetics, Volume 9, Number 4, 1 March 2000 , pp. 477-488(12)

Publisher: Oxford University Press

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Abstract:

Microphthalmia with linear skin defects (MLS) is an X-linked dominant, male-lethal syndrome characterized by microphthalmia, aplastic skin and agenesis of the corpus callosum, and is caused by the deletion of a 500 kb critical region in Xp22.3. Our laboratory isolated a novel rho GTPase-activating protein (rhoGAP) gene named ARHGAP6 from the MLS region. ARHGAP6 contains 14 exons encoding a 974 amino acid protein with three putative SH3-binding domains. Because exons 2–14 are deleted in all MLS patients, we hypothesized that ARHGAP6 may be responsible for some of the phenotypic features of MLS. We pursued two approaches to study the function of ARHGAP6 and its role in the pathogenesis of MLS: gene targeting of the rhoGAP domain in mouse embryonic stem cells and in vitro expression studies. Surprisingly, loss of the rhoGAP function of Arhgap6 does not cause any detectable phenotypic or behavioral abnormalities in the mutant mice. Transfected mammalian cells expressing ARHGAP6 lose their actin stress fibers, retract from the growth surface and extend thin, branching processes resembling filopodia. The ARHGAP6 protein co-localizes with actin filaments through an N-terminal domain and recruits F-actin into the growing processes. Mutation of a conserved arginine residue in the rhoGAP domain prevents the loss of stress fibers but has little effect on process outgrowth. These results suggest that ARHGAP6 has two independent functions: one as a GAP with specificity for RhoA and the other as a cytoskeletal protein that promotes actin remodeling.

Document Type: Research article

Affiliations: 1: Molecular and Human Genetics, 2: Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada 3: Pathology and 4: Cell Biology and

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