Selective stimulation of G-6-Pase catalytic subunit but not G-6-P transporter gene expression by glucagon in vivo and cAMP in situ

Am J Physiol Endocrinol Metab. 2004 May;286(5):E795-808. doi: 10.1152/ajpendo.00455.2003. Epub 2004 Jan 13.

Abstract

We recently compared the regulation of glucose-6-phosphatase (G-6-Pase) catalytic subunit and glucose 6-phosphate (G-6-P) transporter gene expression by insulin in conscious dogs in vivo (Hornbuckle LA, Edgerton DS, Ayala JE, Svitek CA, Neal DW, Cardin S, Cherrington AD, and O'Brien RM. Am J Physiol Endocrinol Metab 281: E713-E725, 2001). In pancreatic-clamped, euglycemic conscious dogs, a 5-h period of hypoinsulinemia led to a marked increase in hepatic G-6-Pase catalytic subunit mRNA; however, G-6-P transporter mRNA was unchanged. Here, we demonstrate, again using pancreatic-clamped, conscious dogs, that glucagon is a candidate for the factor responsible for this selective induction. Thus glucagon stimulated G-6-Pase catalytic subunit but not G-6-P transporter gene expression in vivo. Furthermore, cAMP stimulated endogenous G-6-Pase catalytic subunit gene expression in HepG2 cells but had no effect on G-6-P transporter gene expression. The cAMP response element (CRE) that mediates this induction was identified through transient transfection of HepG2 cells with G-6-Pase catalytic subunit-chloramphenicol acetyltransferase fusion genes. Gel retardation assays demonstrate that this CRE binds several transcription factors including CRE-binding protein and CCAAT enhancer-binding protein.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antiporters
  • Catalytic Domain / genetics
  • Catalytic Domain / physiology*
  • Cells, Cultured
  • Cyclic AMP / physiology*
  • Dogs
  • Fatty Acids, Nonesterified / physiology
  • Female
  • Gene Expression Regulation
  • Glucagon / physiology*
  • Glucose Clamp Technique
  • Glucose-6-Phosphatase / genetics
  • Glucose-6-Phosphatase / metabolism*
  • Glycerol / metabolism
  • Hepatocytes / metabolism
  • Insulin / physiology
  • Liver / metabolism*
  • Male
  • Monosaccharide Transport Proteins
  • Phosphotransferases / genetics
  • Phosphotransferases / metabolism*
  • RNA, Messenger / analysis
  • Second Messenger Systems / physiology

Substances

  • Antiporters
  • Fatty Acids, Nonesterified
  • Insulin
  • Monosaccharide Transport Proteins
  • RNA, Messenger
  • glucose 6-phosphate(transporter)
  • Glucagon
  • Cyclic AMP
  • Phosphotransferases
  • Glucose-6-Phosphatase
  • Glycerol