Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization.

The Rho family of GTPases control diverse biological processes, including cell morphology and mitogenesis. We have identified WASP, the protein that is defective in Wiskott-Aldrich syndrome (WAS), as a novel effector for CDC42Hs, but not for the other Rho family members, Rac and Rho. This interaction is dependent on the ...
presence of the G protein-binding domain. Cellular expression of epitope-tagged WASP produces clusters of WASP that are highly enriched in polymerized actin. This clustering is not observed with a C-terminally deleted WASP and is inhibited by coexpression with dominant negative CDC42Hs-N17, but not with dominant negative forms of Rac or Rho. Thus, WASP provides a novel link between CDC42Hs and the actin cytoskeleton, which suggests a molecular mechanism for many of the cellular abnormalities in WAS. The WASP sequence contains two novel domains that are homologous to other proteins involved in action organization.
Mesh Terms:
Actins, Amino Acid Sequence, Animals, Binding Sites, Cell Cycle Proteins, Cell Line, Cercopithecus aethiops, Consensus Sequence, Cytosol, GTP Phosphohydrolases, GTP-Binding Proteins, Guanosine Diphosphate, Guanosine Triphosphate, Humans, Models, Biological, Molecular Sequence Data, Neutrophils, Protein Biosynthesis, Proteins, Recombinant Proteins, Sequence Homology, Amino Acid, Sequence Tagged Sites, Transfection, Wiskott-Aldrich Syndrome, Wiskott-Aldrich Syndrome Protein, cdc42 GTP-Binding Protein
Cell
Date: Mar. 08, 1996
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