PTG, a Protein Phosphatase 1-Binding Protein with a Role in Glycogen Metabolism

Author:

Printen John A.1,Brady Matthew J.2,Saltiel Alan R.1

Affiliation:

1. J. A. Printen and A. R. Saltiel, Department of Physiology, University of Michigan School of Medicine, Ann Arbor, MI 48109, and Department of Cell Biology, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, MI 48105, USA.

2. M. J. Brady, Department of Cell Biology, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, MI 48105, USA.

Abstract

Protein dephosphorylation by phosphatase PP1 plays a central role in mediating the effects of insulin on glucose and lipid metabolism. A PP1C-targeting protein expressed in 3T3-L1 adipocytes (called PTG, for protein targeting to glycogen) was cloned and characterized. PTG was expressed predominantly in insulin-sensitive tissues. In addition to binding and localizing PP1C to glycogen, PTG formed complexes with phosphorylase kinase, phosphorylase a, and glycogen synthase, the primary enzymes involved in the hormonal regulation of glycogen metabolism. Overexpression of PTG markedly increased basal and insulin-stimulated glycogen synthesis in Chinese hamster ovary cells overexpressing the insulin receptor, which do not express endogenous PTG. These results suggest that PTG is critical for glycogen metabolism, possibly functioning as a molecular scaffold.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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