Post-transcriptional regulation of the human transforming growth factor-beta 1 gene

J Biol Chem. 1992 Jul 5;267(19):13702-7.

Abstract

Since many lines of evidence suggest that expression of the transforming growth factor-beta 1 (TGF-beta 1) gene may be regulated post-transcriptionally, we examined the effect of the 5'-untranslated region (UTR) of this gene on TGF-beta 1 expression. For this purpose, fragments of the 840-nucleotide highly GC-rich TGF-beta 1 5'-UTR were inserted into the 5'-UTR of the structural gene for human growth hormone driven by the simian virus 40 early promoter. A portion of the 5'-UTR of TGF-beta 1 mRNA spanning the sequences from +11 to +147 was shown to inhibit growth hormone expression by as much as 22-fold. This effect was cell-specific; growth hormone production was inhibited in PC-3 human prostate adenocarcinoma and A-549 human lung adenocarcinoma cells, while no effect was seen in rat pheochromocytoma PC12 cells, which show efficient translation of endogenous TGF-beta 1 mRNA. Computer analysis showed that this region of the 5'-UTR contained a stable secondary stem-loop structure spanning sequences +49 to +76. This stem-loop region alone is sufficient to inhibit expression of the growth hormone gene, suggesting that it plays an important role in post-transcriptional regulation of TGF-beta 1 gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Chloramphenicol O-Acetyltransferase / genetics
  • Gene Expression Regulation
  • Growth Hormone / genetics
  • Humans
  • Male
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • PC12 Cells
  • Plasmids
  • Promoter Regions, Genetic
  • RNA Processing, Post-Transcriptional*
  • RNA, Messenger / metabolism
  • Rats
  • Transfection
  • Transforming Growth Factor beta / genetics*
  • Tumor Cells, Cultured

Substances

  • RNA, Messenger
  • Transforming Growth Factor beta
  • Growth Hormone
  • Chloramphenicol O-Acetyltransferase