Glucose regulation of insulin gene expression requires the recruitment of p300 by the beta-cell-specific transcription factor Pdx-1

Mol Endocrinol. 2004 Sep;18(9):2279-90. doi: 10.1210/me.2003-0463. Epub 2004 May 27.

Abstract

Regulation of insulin gene expression in response to increases in blood glucose levels is essential for maintaining normal glucose homeostasis; however, the exact mechanisms by which glucose stimulates insulin gene transcription are not known. We have shown previously that glucose stimulates insulin gene expression by causing the hyperacetylation of histone H4 at the insulin promoter. We demonstrate that the histone acetyltransferase p300 is recruited to the insulin promoter only at high concentrations of glucose via its interaction with the beta-cell-specific transcription factor Pdx-1. Disruption of the function of the endogenous Pdx-1 abolishes the recruitment of p300 to the insulin gene promoter at high concentrations of glucose and results in decreased histone H4 acetylation and insulin gene expression. Furthermore, we demonstrate that the glucose-dependent interaction of Pdx-1 with p300 is regulated by a phosphorylation event that changes the localization of Pdx-1. Based on these data, we conclude that hyperacetylation of histone H4 at the insulin gene promoter in response to high concentrations of glucose depends on the beta-cell-specific transcription factor Pdx-1, which is required for the recruitment of the histone acetyltransferase p300 to the insulin gene promoter.

Publication types

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

MeSH terms

  • Acetylation
  • Acetyltransferases / analysis
  • Acetyltransferases / metabolism*
  • Animals
  • Blood Glucose / physiology
  • Cell Cycle Proteins / analysis
  • Cell Cycle Proteins / metabolism*
  • Cells, Cultured
  • Gene Expression Regulation*
  • Glucose / pharmacology*
  • Glucose / physiology
  • Histone Acetyltransferases
  • Histones / metabolism
  • Homeodomain Proteins / analysis
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Immunoprecipitation
  • Insulin / genetics*
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / immunology
  • Islets of Langerhans / metabolism*
  • Mice
  • Okadaic Acid / pharmacology
  • Promoter Regions, Genetic / genetics
  • Rats
  • Trans-Activators / analysis
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription Factors
  • p300-CBP Transcription Factors

Substances

  • Blood Glucose
  • Cell Cycle Proteins
  • Histones
  • Homeodomain Proteins
  • Insulin
  • Trans-Activators
  • Transcription Factors
  • pancreatic and duodenal homeobox 1 protein
  • Okadaic Acid
  • Acetyltransferases
  • Histone Acetyltransferases
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor
  • Glucose