Insulin promotes phosphorylation and activation of geranylgeranyltransferase II. Studies with geranylgeranylation of rab-3 and rab-4

• Published in: The Journal of biological chemistry Vol. 274; no. 5; pp. 2880 - 2884
• Main Authors: Goalstone, M L, Leitner, J W, Golovchenko, I, Stjernholm, M R, Cormont, M, Le Marchand-Brustel, Y, Draznin, B
• Format: Journal Article
• Language: English
• Published: United States 29.01.1999
• Subjects: 3T3 Cells; Adipocytes - drug effects; Adipocytes - enzymology; Alkyl and Aryl Transferases - metabolism; Androstadienes - pharmacology; Animals; Enzyme Activation; Enzyme Inhibitors - pharmacology; Fibroblasts - drug effects; Fibroblasts - enzymology; GTP-Binding Proteins - metabolism; Insulin - pharmacology; Mice; Phosphorylation; rab3 GTP-Binding Proteins; rab4 GTP-Binding Proteins; Wortmannin
• ISSN: 0021-9258
• DOI: 10.1074/jbc.274.5.2880

Rab proteins play a crucial role in the trafficking of intracellular vesicles. Rab proteins are GTPases that cycle between an inactive GDP-bound form and an active GTP-bound conformation. A prerequisite to Rab activation by GTP loading is its post-translational modification by the addition of geranylgeranyl moieties to highly conserved C-terminal cysteine residues. We examined the effect of insulin on the activity of geranylgeranyltransferase II (GGTase II) in 3T3-L1 fibroblasts and adipocytes. In fibroblasts, insulin increased the enzymatic activity of GGTase II 2.5-fold after 1 h of incubation, an effect that is blocked by perillyl alcohol, an inhibitor of prenyltransferases, but not by the geranylgeranyltransferase I inhibitor, GGTI-298, or the farnesyltransferase inhibitor, alpha-hydroxyfarnesylphosphonic acid. Concomitantly, insulin stimulated the phosphorylation of the GGTase II alpha-subunit without any effect on the GGTase II beta-subunit. At the same time, insulin also increased the amounts of geranylgeranylated Rab-3 in 3T3-L1 fibroblasts from 44 +/- 1.2% in control cells to 63 +/- 3.8 and 64 +/- 6.1% after 1 and 24 h of incubation, respectively. In adipocytes, insulin increased the amounts of geranylgeranylated Rab-4 from 38 +/- 0.6% in control cells to 56 +/- 1.7 and 60 +/- 2.6% after 1 and 24 h of incubation, respectively. In both fibroblasts and adipocytes, the presence of perillyl alcohol blocked the ability of insulin to increase geranylgeranylation of Rab-4, whereas GGTI-298 and alpha-hydroxyfarnesylphosphonic acid were without effect, indicating that insulin activates GGTase II. In summary, insulin promotes phosphorylation and activation of GGTase II in both 3T3 L1 fibroblasts and adipocytes and increases the amounts of geranylgeranylated Rab-3 and Rab-4 proteins.