Insulin gene expression in nonexpressing cells appears to be regulated by multiple distinct negative-acting control elements

Mol Cell Biol. 1991 May;11(5):2881-6. doi: 10.1128/mcb.11.5.2881-2886.1991.

Abstract

Selective transcription of the insulin gene in pancreatic beta cells is regulated by its enhancer, located between nucleotides -340 and -91 relative to the transcription start site. Transcription from the enhancer is controlled by both positive- and negative-acting cellular factors. Cell-type-specific expression is mediated principally by a single cis-acting enhancer element located between -100 and -91 in the rat insulin II gene (referred to as the insulin control element [ICE]), which is acted upon by both of these cellular activities. Analysis of the effect of 5' deletions within the insulin enhancer has identified a region between nucleotides -217 and -197 that is also a site of negative control. Deletion of these sequences from the 5' end of the enhancer leads to transcription of the enhancer in non-insulin-producing cells, even though the ICE is intact. Derepression of this ICE-mediated effect was shown to be due to the binding of a ubiquitously distributed cellular factor to a sequence element which resides just upstream of the ICE (i.e., between nucleotides -110 and -100). We discuss the possible relationship of these results to cell-type-specific regulation of the insulin gene.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Chromosome Deletion
  • DNA-Binding Proteins / metabolism
  • Enhancer Elements, Genetic
  • Gene Expression Regulation*
  • Genes*
  • HeLa Cells / physiology
  • Humans
  • Insulin / genetics*
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Oligonucleotide Probes
  • Rats
  • Transcription, Genetic*

Substances

  • DNA-Binding Proteins
  • Insulin
  • Oligonucleotide Probes