Characterization of TCL, a new GTPase of the Rho family related to TC10 and Cdc42

被引:97
|
作者
Vignal, E
De Toledo, M
Comunale, F
Ladopoulou, A
Gauthier-Rouviere, C
Blangy, A
Fort, P
机构
[1] Ctr Rech Biochim Macromol, CNRS UPR 1086, F-34293 Montpellier 5, France
[2] Demokritos Natl Ctr Sci Res, Inst Radioisotopes & Radiodiagnost Prod, Mol Diagnost Lab, Athens 15310, Greece
关键词
D O I
10.1074/jbc.M003487200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
GTPases of the Rho family control a wide variety of cellular processes such as cell morphology, motility, proliferation, differentiation, and apoptosis, We report here the characterization of a new Rho member, which shares 85% and 78% amino acid similarity to TC10 and Cdc42, respectively. This GTPase, termed as TC10-like (TCL) is encoded by an unexpectedly large locus, made of five exons spanning over 85 kilobases on human chromosome 14, TCL mRNA is 2.5 kilobases long and is mainly expressed in heart. In vitro, TCL shows rapid GDP/GTP exchange and displays higher GTP dissociation and hydolysis rates than TC10, Using the yeast two-hybrid system and GST pull-down assays, we show that GTP-bound but not GDP-bound TCL protein directly interacts with Cdc42/Rac interacting binding domains, such as those found in PAK and WASP. Despite its overall similarity to TC10 and Cdc42, the constitutively active TCL mutant displays distinct morphogenic activity in REF-52 fibroblasts, producing large and dynamic F-actin-rich ruffles on the dorsal cell membrane. Interestingly, TCL morphogenic activity is blocked by dominant negative Rad and Cdc42 mutants, suggesting a crosstalk between these three Rho GTPases.
引用
收藏
页码:36457 / 36464
页数:8
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