The repression of hormone-activated PEPCK gene expression by glucose is insulin-independent but requires glucose metabolism

J Biol Chem. 1998 Sep 11;273(37):24145-51. doi: 10.1074/jbc.273.37.24145.

Abstract

Phosphoenolpyruvate carboxykinase (PEPCK) is a rate-controlling enzyme in hepatic gluconeogenesis, and it therefore plays a central role in glucose homeostasis. The rate of transcription of the PEPCK gene is increased by glucagon (via cAMP) and glucocorticoids and is inhibited by insulin. Under certain circumstances glucose also decreases PEPCK gene expression, but the mechanism of this effect is poorly understood. The glucose-mediated stimulation of a number of glycolytic and lipogenic genes requires the expression of glucokinase (GK) and increased glucose metabolism. HL1C rat hepatoma cells are a stably transfected line of H4IIE rat hepatoma cells that express a PEPCK promoter-chloramphenicol acetyltransferase fusion gene that is regulated in the same manner as the endogenous PEPCK gene. These cells do not express GK and do not normally exhibit a response of either the endogenous PEPCK gene, or of the trans-gene, to glucose. A recombinant adenovirus that directs the expression of glucokinase (AdCMV-GK) was used to increase glucose metabolism in HL1C cells to test whether increased glucose flux is also required for the repression of PEPCK gene expression. In AdCMV-GK-treated cells glucose strongly inhibits hormone-activated transcription of the endogenous PEPCK gene and of the expressed fusion gene. The glucose effect on PEPCK gene promoter activity is blocked by 5 mM mannoheptulose, a specific inhibitor of GK activity. The glucose analog, 2-deoxyglucose mimics the glucose response, but this effect does not require GK expression. 3-O-methylglucose is ineffective. Glucose exerts its effect on the PEPCK gene within 4 h, at physiologic concentrations, and with an EC50 of 6.5 mM, which approximates the Km of glucokinase. The effects of glucose and insulin on PEPCK gene expression are additive, but only at suboptimal concentrations of both agents. The results of these studies demonstrate that, by inhibiting PEPCK gene transcription, glucose participates in a feedback control loop that governs its production from gluconeogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Chloramphenicol O-Acetyltransferase
  • Cytomegalovirus
  • Enzyme Repression
  • Genetic Vectors
  • Glucokinase / biosynthesis
  • Glucokinase / genetics
  • Glucose / metabolism*
  • Glucose / pharmacology*
  • Glycolysis
  • Homeostasis
  • Insulin / pharmacology
  • Insulin / physiology*
  • Kinetics
  • Liver Neoplasms, Experimental / metabolism*
  • Phosphoenolpyruvate Carboxykinase (GTP) / biosynthesis*
  • Phosphoenolpyruvate Carboxykinase (GTP) / genetics*
  • Promoter Regions, Genetic
  • Rats
  • Recombinant Fusion Proteins / biosynthesis
  • Transcription, Genetic*
  • Transfection

Substances

  • Insulin
  • Recombinant Fusion Proteins
  • Chloramphenicol O-Acetyltransferase
  • Glucokinase
  • Phosphoenolpyruvate Carboxykinase (GTP)
  • Glucose