Identification of a Rho family specific guanine nucleotide exchange factor, FLJ00018, as a novel actin-binding protein

2013 ◽  
Vol 25 (1) ◽  
pp. 41-49 ◽  
Author(s):  
Katsuya Sato ◽  
Hiroaki Handa ◽  
Masashi Kimura ◽  
Yukio Okano ◽  
Hitoshi Nagaoka ◽  
...  
Keyword(s):  
Binding Protein ◽  
Guanine Nucleotide Exchange Factor ◽  
Actin Binding ◽  
Guanine Nucleotide ◽  
Nucleotide Exchange ◽  
Actin Binding Protein ◽  
Exchange Factor ◽  
Guanine Nucleotide Exchange ◽  
Nucleotide Exchange Factor ◽  
Rho Family

scholarly journals The Rho Family Guanine Nucleotide Exchange Factor Vav-2 Regulates the Development of Cell-Mediated Cytotoxicity

2000 ◽  
Vol 192 (3) ◽  
pp. 381-392 ◽  
Author(s):  
Daniel D. Billadeau ◽  
Stacy M. Mackie ◽  
Renee A. Schoon ◽  
Paul J. Leibson
Keyword(s):  
Guanine Nucleotide Exchange Factor ◽  
Cytotoxic Lymphocytes ◽  
Guanine Nucleotide ◽  
Cellular Cytotoxicity ◽  
Nucleotide Exchange ◽  
Exchange Factor ◽  
Guanine Nucleotide Exchange ◽  
Activating Receptors ◽  
Nucleotide Exchange Factor ◽  
Rho Family

Previous pharmacologic and genetic studies have demonstrated a critical role for the low molecular weight GTP-binding protein RhoA in the regulation of cell-mediated killing by cytotoxic lymphocytes. However, a specific Rho family guanine nucleotide exchange factor (GEF) that activates this critical regulator of cellular cytotoxicity has not been identified. In this study, we provide evidence that the Rho family GEF, Vav-2, is present in cytotoxic lymphocytes, and becomes tyrosine phosphorylated after the cross-linking of activating receptors on cytotoxic lymphocytes and during the generation of cell-mediated killing. In addition, we show that overexpression of Vav-2 in cytotoxic lymphocytes enhances cellular cytotoxicity, and this enhancement requires a functional Dbl homology and Src homology 2 domain. Interestingly, the pleckstrin homology domain of Vav-2 was found to be required for enhancement of killing through some, but not all activating receptors on cytotoxic lymphocytes. Lastly, although Vav and Vav-2 share significant structural homology, only Vav is able to enhance nuclear factor of activated T cells–activator protein 1–mediated gene transcription downstream of the T cell receptor. These data demonstrate that Vav-2, a Rho family GEF, differs from Vav in the control of certain lymphocyte functions and participates in the control of cell-mediated killing by cytotoxic lymphocytes.

scholarly journals Lck regulates Vav activation of members of the Rho family of GTPases.

1997 ◽  
Vol 17 (3) ◽  
pp. 1346-1353 ◽  
Author(s):  
J Han ◽  
B Das ◽  
W Wei ◽  
L Van Aelst ◽  
R D Mosteller ◽  
...  
Keyword(s):  
Animal Cell ◽  
Guanine Nucleotide Exchange Factor ◽  
Biological Data ◽  
Guanine Nucleotide ◽  
Nucleotide Exchange ◽  
Exchange Factor ◽  
Guanine Nucleotide Exchange ◽  
Nucleotide Exchange Factor ◽  
Rho Family

Vav is a member of a family of oncogene proteins that share an approximately 250-amino-acid motif called a Dbl homology domain. Paradoxically, Dbl itself and other proteins containing a Dbl domain catalyze GTP-GDP exchange for Rho family proteins, whereas Vav has been reported to catalyze GTP-GDP exchange for Ras proteins. We present Saccharomyces cerevisiae genetic data, in vitro biochemical data, and animal cell biological data indicating that Vav is a guanine nucleotide exchange factor for Rho-related proteins, but in similar genetic and biochemical experiments we fail to find evidence that Vav is a guanine nucleotide exchange factor for Ras. Further, we present data indicating that the Lck kinase activates the guanine nucleotide exchange factor and transforming activity of Vav.

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