Characterization of TCL, a New GTPase of the Rho Family related to TC10 and Cdc42* 210
By E. Vignal, M. de Toledo, F. Comunale, A. Ladopoulou, C. Gauthier-Rouvière, A. Blangy, P. Fort. Journal of Biological Chemistry, 2000
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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 Rac1 and Cdc42 mutants, suggesting a cross-talk between these three Rho GTPases.
Subfields: Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/66536940f42aef949889bf4638d69d36a2d31547
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Citations in the corpus
- Rho GTPase signalling in cell migration (2015, background): “b-PIX is a GEF for Rac1 and Cdc42 [16] and RhoJ and b-PIX also interact with Rac/Cdc42-activated PAK kinases [33,36], but whether RhoJ activates either of these proteins is not known.”
- Rho-family GTPases: it's not only Rac and Rho (and I like it) (2004, background): “NC 27599-7295, USA *Author for correspondence (e-mail: krister@med.unc.edu) Journal of Cell Science 117, 1301-1312 Published by The Company of Biologists 2004 doi:10.1242/jcs.01118 Commentary 1302 RhoG]; the Cdc42-related subfamily [Cdc42 (and its brainspecific C-terminal splice variant G25K), TC10,”