A role for Rac in Tiaml-induced membrane ruffling and invasion
- 1 May 1995
- journal article
- Published by Springer Nature in Nature
- Vol. 375 (6529) , 338-340
- https://doi.org/10.1038/375338a0
Abstract
Rho-like GTPases have been implicated in the regulation of the actin cytoskeleton which controls the morphology, adhesion and motility of cells. Like Ras proteins, they become activated when bound GDP is exchanged for GTP, a process catalysed by GDP-dissociation stimulator (GDS) proteins. Several GDS proteins specific for Rho-like GTPases have been identified. Most of these contain a conserved catalytic domain, the DBL-homology (DH) domain, and activate Cdc42 or Rho but not Rac. We have isolated the invasion-inducing Tiam1 gene, which also encodes a protein with a DH domain. Here we show that Tiam1 is a GDS protein for Rho-like GTPases in vitro. In fibroblasts, Tiam1 induces a similar phenotype as constitutively activated (V12)Rac1, including membrane ruffling, and this is inhibited by dominant negative (N17)Rac1. Moreover, T-lymphoma cells expressing V12Rac1 become invasive, indicating that the Tiam1-Rac signalling pathway could be operating in the invasion and metastasis of tumour cells.Keywords
This publication has 25 references indexed in Scilit:
- SmgGDS stabilizes nucleotide-bound and -free forms of the Rac1 GTP-binding protein and stimulates GTP/GDP exchange through a substituted enzyme mechanismBiochemical Journal, 1994
- Identification of an invasion-inducing gene, Tiam-1, that encodes a protein with homology to GDP-GTP exchangers for Rho-like proteinsCell, 1994
- Proteins regulating Ras and its relativesNature, 1993
- Inhibition of PMA-induced, LFA-1-dependent lymphocyte aggregation by ADP ribosylation of the small molecular weight GTP binding protein, rho.The Journal of cell biology, 1993
- Involvement of rho p21 and its inhibitory GDP/GTP exchange protein (rho GDI) in cell motility.Molecular and Cellular Biology, 1993
- The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factorsCell, 1992
- Ras-related GTPases and the cytoskeleton.Molecular Biology of the Cell, 1992
- Both stimulatory and inhibitory GDPGTP exchange proteins, smg GDS and rho GDI, are active on multiple small GTP-binding proteinsBiochemical and Biophysical Research Communications, 1992
- Catalysis of guanine nucleotide exchange on the CDC42Hs protein by the dbloncogene productNature, 1991
- Molecular cloning of the gene for the human placental GTP-binding protein Gp (G25K): identification of this GTP-binding protein as the human homolog of the yeast cell-division-cycle protein CDC42.Proceedings of the National Academy of Sciences, 1990