Mitogenic signals control translation of the early growth response gene-1 in myogenic cells

Biochem Biophys Res Commun. 1994 Aug 15;202(3):1337-46. doi: 10.1006/bbrc.1994.2077.

Abstract

Muscle is a major site of expression of the early growth response gene-1 (Egr-1). To investigate its role in muscle proliferation and/or differentiation we studied the effect of a variety of growth factors on cultured mouse muscle Sol8 cells. Three groups of responses could be distinguished: 1. AII, endothelin, phenylephrine, and PMA induced Egr-1 mRNA accumulation, but the message remained untranslated. These factors induced neither differentiation nor proliferation. 2. Insulin induced differentiation. It stimulated Egr-1 mRNA accumulation, but no translation into the Egr-1 protein was seen. 3. bFGF, PDGF BB, and FCS strongly induced DNA- and protein synthesis (i.e. proliferation) and Egr-1 mRNA accumulation. Only under these conditions was the message translated into protein. We conclude: 1. AII, endothelin, phenylephrine, and PMA elicit a nuclear response in Sol8 muscle cells which may lead to reprogramming of genes unrelated to differentiation or proliferation. 2. Differentiation induces a translational block of the Egr-1 mRNA which is only relieved by mitotic stimuli. 3. These results strongly suggest a pivotal role of Egr-1 in muscle proliferation and define translational control as a new mechanism of Egr-1 regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II / pharmacology
  • Animals
  • Base Sequence
  • Becaplermin
  • Cells, Cultured
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Early Growth Response Protein 1
  • Endothelins / pharmacology
  • Fibroblast Growth Factor 2 / pharmacology
  • Immediate-Early Proteins*
  • Insulin / pharmacology
  • Mice
  • Molecular Sequence Data
  • Muscles / cytology
  • Muscles / drug effects
  • Muscles / metabolism*
  • Oligodeoxyribonucleotides
  • Phenylephrine / pharmacology
  • Platelet-Derived Growth Factor / pharmacology
  • Protein Biosynthesis*
  • Proto-Oncogene Proteins c-sis
  • Signal Transduction*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transforming Growth Factor beta / pharmacology
  • Zinc Fingers / genetics*

Substances

  • DNA-Binding Proteins
  • Early Growth Response Protein 1
  • Egr1 protein, mouse
  • Endothelins
  • Immediate-Early Proteins
  • Insulin
  • Oligodeoxyribonucleotides
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • Transcription Factors
  • Transforming Growth Factor beta
  • Fibroblast Growth Factor 2
  • Angiotensin II
  • Becaplermin
  • Phenylephrine
  • Tetradecanoylphorbol Acetate