Transcription factor cycling on the insulin promoter

FEBS Lett. 2006 Jan 23;580(2):711-5. doi: 10.1016/j.febslet.2005.12.061. Epub 2005 Dec 28.

Abstract

Using MIN6 beta-cells and chromatin immunoprecipitation (ChIP) assays, the chronological sequence of binding of MafA, E47/beta2 and PDX-1 to the insulin promoter in living beta-cells were investigated. All four factors were shown to bind to the mouse insulin 2 promoter in a cyclical manner with a periodicity of approximately 10-15 min. The cyclical binding of MafA, E47 and beta2 was largely unaffected by the glucose or insulin concentration in the media. However, the binding and cycling of PDX-1 was markedly abolished in low glucose (1 mM), and this was reversed in the presence of low concentrations of insulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Glucose / metabolism
  • Homeodomain Proteins / metabolism*
  • Humans
  • Insulin / genetics*
  • Insulin / metabolism
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / metabolism
  • Maf Transcription Factors, Large / metabolism*
  • Mice
  • Molecular Sequence Data
  • Promoter Regions, Genetic*
  • Protein Binding
  • Sequence Alignment
  • TCF Transcription Factors / metabolism*
  • Trans-Activators / metabolism*
  • Transcription Factor 7-Like 1 Protein

Substances

  • Homeodomain Proteins
  • Insulin
  • Maf Transcription Factors, Large
  • Mafa protein, mouse
  • TCF Transcription Factors
  • TCF7L1 protein, human
  • Tcf7l1 protein, mouse
  • Trans-Activators
  • Transcription Factor 7-Like 1 Protein
  • pancreatic and duodenal homeobox 1 protein
  • Glucose