The atypical Rho family GTPase Wrch-1 regulates focal adhesion formation and cell migration

Author:

Chuang Ya-yu1,Valster Aline1,Coniglio Salvatore J.12,Backer Jonathan M.3,Symons Marc124

Affiliation:

1. Center for Oncology and Cell Biology, The Feinstein Institute for Medical Research at North Shore-LIJ, North Shore University Hospital, Manhasset, NY 11030, USA

2. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

3. Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

4. Department of Surgery, North Shore University Hospital, Manhasset, NY 11030, USA

Abstract

Wrch-1 (Wnt-regulated Cdc42 homolog) is a new member of the Rho family that was identified as a gene transcriptionally upregulated by Wnt-1. Wrch-1 has no detectable GTPase activity and displays very high intrinsic guanine nucleotide exchange, implying that it is constitutively GTP-bound. The biological functions of Wrch-1 largely remain to be characterized. Here, we report that Wrch-1 prominently localizes to focal adhesions. Depletion of Wrch-1 by small interfering RNA increases focal adhesion formation, whereas Wrch-1 overexpression disassembles focal adhesions. Wrch-1 depletion inhibits myosin-light-chain phosphorylation, which in turn leads to an increase in the number of focal adhesions and inhibits cell migration in response to wound healing. Depletion of Wrch-1 also inhibits Akt and JNK activation. Although pharmacological inhibitors of Akt and JNK inhibit cell migration, they do not affect focal adhesions. Thus, our data suggest that Wrch-1 regulates cell migration by multiple mechanisms: on the one hand Wrch-1 controls focal adhesions by regulating myosin light chain and on the other hand Wrch-1 stimulates the activation of Akt and JNK.

Publisher

The Company of Biologists

Subject

Cell Biology

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