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

Weifeng Luo
Radoslav Janoštiak
Ondřej Tolde
Larisa M Ryzhova
Lenka Koudelková
Michal Dibus
Jan Brábek
Steven K Hanks
Daniel Rosel

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 called 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. ARHGAP42 regulation was investigated by expression in mammalian cells. 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.