The major objective of this research is to determine how renal glycogen synthase is regulated and to apply any new insights gained to the regulation of glycogen synthase in other mammalian tissues. While much is known about the regulation of glycogen synthase in tissues with relatively high concentrations of glycogen, little is known about the regulation of glycogen synthase in tissues which contain relatively low concentrations of glycogen. Of particular interest is the kidney since there is a large difference in the synthesis of glycogen in the cortex and medulla even though glycogen levels are low in both portions of the kidney. The specific goals of this project are: 1) To purify and characterize renal glycogen synthase kinases and to establish the physiological significance and regulation of these enzymes in the medulla and cortex. Special emphasis will be placed on the role of cyclic AMP-independent glycogen synthase kinases as well as cyclic AMP-dependent protein kinase. 2) To purify and characterize renal glycogen synthase I and D and to establish how they are regulated in the cortex and medulla. 3) To purify and characterize renal glycogen synthase phosphatases and to establish their physiological significance and regulation in the cortex and medulla.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK014723-16
Application #
3225273
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1977-05-01
Project End
1989-04-30
Budget Start
1988-05-01
Budget End
1989-04-30
Support Year
16
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Toledo
Department
Type
Schools of Medicine
DUNS #
807418939
City
Toledo
State
OH
Country
United States
Zip Code
43614
Schlender, K K; Wang, W; Wilson, S E (1989) Evidence for a latent form of protein phosphatase 1 associated with cardiac myofibrils. Biochem Biophys Res Commun 159:72-8
Hegazy, M G; Schlender, K K; Wilson, S E et al. (1989) Inhibitory effect of polycations on phosphorylation of glycogen synthase by glycogen synthase kinase 3. Biochim Biophys Acta 1011:198-204
Jakes, S; Hastings, T G; Reimann, E M et al. (1988) Identification of the phosphoserine residue in histone H1 phosphorylated by protein kinase C. FEBS Lett 234:31-4
Schlender, K K; Thysseril, T J; Hegazy, M G (1988) Calcium-dependent phosphorylation of bovine cardiac C-protein by phosphorylase kinase. Biochem Biophys Res Commun 155:45-51
Jakes, S; Schlender, K K (1988) Histone H1 phosphorylated by protein kinase C is a selective substrate for the assay of protein phosphatase 2A in the presence of phosphatase 1. Biochim Biophys Acta 967:11-6
Hegazy, M G; Thysseril, T J; Schlender, K K et al. (1987) Characterization of GSK-M, a glycogen synthase kinase from rat skeletal muscle. Arch Biochem Biophys 258:470-81