Epidermal growth factor stimulates transcription of the c-jun proto-oncogene in rat fibroblasts

Nature. 1988 Aug 11;334(6182):538-9. doi: 10.1038/334538a0.

Abstract

Some growth factor-induced genes, such as the c-fos gene, are activated rapidly and transiently without intervening protein synthesis. Others, like the rat transin gene, are activated more slowly but more durably and their activation requires prior protein synthesis. It is tempting to speculate that certain rapidly-activated genes code for transcription factors which interact directly with promoter regions of genes like the transin gene to trigger their expression. Unfortunately, little is known about the majority of primary response genes to support this hypothesis. The proto-oncogene c-jun codes for the transcription factor AP-1 or a closely related protein. We show that epidermal growth factor stimulates transcription of the c-jun gene in fibroblasts as a primary response. This supports the notion that increased expression of genes encoding transcription factors is an important element of the signal transduction mechanism, assuring the long-term transcriptional response of cells to growth factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amanitins / pharmacology
  • Animals
  • Cycloheximide / pharmacology
  • DNA / genetics
  • DNA-Binding Proteins / genetics*
  • Epidermal Growth Factor / pharmacology*
  • Fibroblasts / metabolism*
  • Humans
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Proto-Oncogenes*
  • RNA, Messenger / biosynthesis
  • Rats
  • Transcription Factors / genetics*
  • Transcription, Genetic* / drug effects

Substances

  • Amanitins
  • DNA-Binding Proteins
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • Transcription Factors
  • Epidermal Growth Factor
  • DNA
  • Cycloheximide