Insulin regulation of glucokinase gene expression: evidence against a role for sterol regulatory element binding protein 1 in primary hepatocytes

FEBS Lett. 2006 Jan 23;580(2):410-4. doi: 10.1016/j.febslet.2005.12.032. Epub 2005 Dec 20.

Abstract

Liver key genes for carbohydrate and lipid homeostasis are regulated by insulin and glucose. The sterol regulatory-element binding protein-1c (SREBP-1c) has emerged as a mediator of insulin effects on gene transcription, particularly on glucokinase (GK). In this paper, we show that despite stimulation of GK promoter transcription by overexpression of mature SREBP-1c, insulin induced GK transcription at least 4h ahead of accumulation of mature SREBP-1c in the nucleus. Importantly, the knockdown of SREBP-1 mRNA using a RNA-interference technique reduced the level of nuclear SREBP-1 protein, diminished fatty acid synthase mRNA level, but did not affect GK and L-pyruvate kinase mRNA levels. We concluded that SREBP-1 is unlikely to be the mediator of the early insulin effect on GK gene transcription.

MeSH terms

  • Animals
  • Cells, Cultured
  • Gene Expression Regulation, Enzymologic*
  • Gene Silencing
  • Glucokinase / genetics
  • Glucokinase / metabolism*
  • Hepatocytes / cytology
  • Hepatocytes / metabolism*
  • Insulin / metabolism*
  • Male
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Wistar
  • Sterol Regulatory Element Binding Protein 1 / genetics
  • Sterol Regulatory Element Binding Protein 1 / metabolism*
  • Transcription, Genetic

Substances

  • Insulin
  • RNA, Small Interfering
  • Sterol Regulatory Element Binding Protein 1
  • Glucokinase