By Margaret A. Shupnik

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Convergence and divergence of multiple branching pathways, subcellular compartmentalization, tissue-specific expression of key effectors, and modulation of signal frequency and amplitude are among the potential mechanisms underlying specificity in insulin signaling. REFERENCES 1. Ullrich A, Bell JR, Chen EY, Herrera R, Petruzzelli LM, Dull TJ, Gray A, Coussens L, Liao YC, Tsubokawa M, Mason A, Seepurg PH, Grunfeld C, Rosen OM, Ramachandran J. Human insulin receptor and its relationship to the tyrosine kinase family of oncogenes.

Insulin-mediated targeting of phosphatidylinositol 3-kinase to GLUT4-containing vesicles. J Biol Chem 1996; 271:10,200–10,204. Parton RG. Caveolae and caveolins. Curr Opin Cell Biol 1996; 8:542–548. Faux MC, Scott JD. Molecular glue: kinase anchoring and scaffold proteins. Cell 1996; 85:9–12. 38 Quon and Taylor 123. Liu P, Ying Y-S, Anderson RGW. Platelet-derived growth factor activates mitogen-activated protein kinase in isolated caveolae. Proc Natl Acad Sci USA 1997; 94:13,666–13,670. 124. Couet J, Sargiacomo M, Lisanti MP.

Science 1996; 272:227–234. Rea S, James DE. Moving GLUT4: the biogenesis and trafficking of GLUT4 storage vesicles. Diabetes 1997; 46:1667–1677. Cain CC, Trimble WS, Lienhard GE. Members of the VAMP family of synaptic vesicle proteins are components of glucose transporter-containing vesicles from rat adipocytes. J Biol Chem 1992; 267:11,681–11,684. Martin S, Tellam J, Livingstone C, Slot JW, Gould GW, James DE. The glucose transporter (GLUT4) and vesicle-associated membrane protein-2 (VAMP-2) are segregated from recycling endosomes in insulin-sensitive cells.

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