Accessory elements, flanking DNA sequence, and promoter context play key roles in determining the efficacy of insulin and phorbol ester signaling through the malic enzyme and collagenase-1 AP-1 motifs

J Biol Chem. 2002 Aug 2;277(31):27935-44. doi: 10.1074/jbc.M203682200. Epub 2002 May 24.

Abstract

Insulin stimulates malic enzyme (ME)-chloramphenicol acetyltransferase (CAT) and collagenase-1-CAT fusion gene expression in H4IIE cells through identical activator protein-1 (AP-1) motifs. In contrast, insulin and phorbol esters only stimulate collagenase-1-CAT and not ME-CAT fusion gene expression in HeLa cells. The experiments in this article were designed to explore the molecular basis for this differential cell type- and gene-specific regulation. The results highlight the influence of three variables, namely promoter context, AP-1 flanking sequence, and accessory elements that modulate insulin and phorbol ester signaling through the AP-1 motif. Thus, fusion gene transfection and proteolytic clipping gel retardation assays suggest that the AP-1 flanking sequence affects the conformation of AP-1 binding to the collagenase-1 and ME AP-1 motifs such that it selectively binds the latter in a fully activated state. However, this influence of ME AP-1 flanking sequence is dependent on promoter context. Thus, the ME AP-1 motif will mediate both an insulin and phorbol ester response in HeLa cells when introduced into either the collagenase-1 promoter or a specific heterologous promoter. But even in the context of the collagenase-1 promoter, the effects of both insulin and phorbol esters, mediated through the ME AP-1 motif are dependent on accessory factors.

Publication types

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

MeSH terms

  • Base Sequence
  • Cell Line
  • Chloramphenicol O-Acetyltransferase / genetics
  • Collagenases / genetics*
  • DNA Primers
  • Gene Expression Regulation, Enzymologic / drug effects
  • HeLa Cells
  • Humans
  • Insulin / physiology*
  • Malate Dehydrogenase / genetics*
  • Mutagenesis
  • Oligodeoxyribonucleotides
  • Phorbol Esters / pharmacology*
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic*
  • Recombinant Proteins / metabolism
  • Transcription Factor AP-1 / metabolism*
  • Transcription Factors / metabolism*
  • Transfection
  • beta-Galactosidase / genetics

Substances

  • DNA Primers
  • Insulin
  • Oligodeoxyribonucleotides
  • Phorbol Esters
  • Recombinant Proteins
  • Transcription Factor AP-1
  • Transcription Factors
  • Malate Dehydrogenase
  • Chloramphenicol O-Acetyltransferase
  • beta-Galactosidase
  • Collagenases
  • collagenase 1