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Identification and characterization of a novel Rho GTPase activating protein implicated in receptor-mediated endocytosis

Authors :
Toshihiro Nukiwa
Hiroshi Takeshima
Tomohiro Sakakibara
Yasuo Nemoto
Source :
FEBS Letters. (1-3):294-300
Publisher :
Federation of European Biochemical Societies. Published by Elsevier B.V.

Abstract

Cbl-interacting protein of 85 kDa (CIN85) is a recently identified adaptor protein involved in the endocytic process of several receptor tyrosine kinases. Here we have identified a novel RhoGAP, CIN85 associated multi-domain containing RhoGAP1 (CAMGAP1) as a binding protein for CIN85. CAMGAP1 is composed of an Src homology 3 (SH3) domain, multiple WW domains, a proline-rich region, a PH domain and a RhoGAP domain, and has the domain architecture similar to ARHGAP9 and ARHGAP12. CAMGAP1 mRNA is widely distributed in murine tissues. Biochemical assays showed its GAP activity toward Rac1 and Cdc42. Protein binding and expression studies indicated that the second SH3 domain of CIN85 binds to a proline-rich region of CAMGAP1. Overexpression of a truncated form of CAMGAP1 interferes with the internalization of transferrin receptors, suggesting that CAMGAP1 may play a role in clathrin-mediated endocytosis.

Details

Language :
English
ISSN :
00145793
Issue :
1-3
Database :
OpenAIRE
Journal :
FEBS Letters
Accession number :
edsair.doi.dedup.....1176bb557a0662c31517cde31f42df0a
Full Text :
https://doi.org/10.1016/j.febslet.2004.03.101