ARHGAP42 is activated by Src-mediated tyrosine phosphorylation to promote cell motility.

Document Type

Article

Publication Date

7-15-2017

Institution/Department

Medical Education

Journal Title

Journal of cell science

MeSH Headings

Animals, Cell Movement, Focal Adhesions, GTPase-Activating Proteins, Humans, Mice, Phosphorylation, Tyrosine, rho GTP-Binding Proteins, rhoA GTP-Binding Protein, src-Family Kinases

Abstract

The tyrosine kinase Src acts as a key regulator of cell motility by phosphorylating multiple protein substrates that control cytoskeletal and adhesion dynamics. In an earlier phosphotyrosine proteomics study, we identified a novel Rho-GTPase activating protein, now known as ARHGAP42, as a likely biologically relevant Src substrate. ARHGAP42 is a member of a family of RhoGAPs distinguished by tandem BAR-PH domains lying N-terminal to the GAP domain. Like other family members, ARHGAP42 acts preferentially as a GAP for RhoA. We show that Src principally phosphorylates ARHGAP42 on tyrosine 376 (Tyr-376) in the short linker between the BAR-PH and GAP domains. The expression of ARHGAP42 variants in mammalian cells was used to elucidate its regulation. We found that the BAR domain is inhibitory toward the GAP activity of ARHGAP42, such that BAR domain deletion resulted in decreased active GTP-bound RhoA and increased cell motility. With the BAR domain intact, ARHGAP42 GAP activity could be activated by phosphorylation of Tyr-376 to promote motile cell behavior. Thus, phosphorylation of ARHGAP42 Tyr-376 is revealed as a novel regulatory event by which Src can affect actin dynamics through RhoA inhibition.

ISSN

1477-9137

First Page

2382

Last Page

2393

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