Expression and induction by IL-6 of the normal and variant genes for human plasminogen

Biochem Biophys Res Commun. 1997 Jan 3;230(1):129-32. doi: 10.1006/bbrc.1996.5909.

Abstract

We examined the promoter activity of the gene for human plasminogen (PLG) employing its 1.1 kb fragment of the 5'-flanking region inserted in front of a reporter gene. Deletion analysis revealed that a region surrounding the transcription start site was essential for the PLG expression. Since the PLG gene has three sequences for the interleukin-6 (IL-6) responsive element, we examined the effect of IL-6 on the PLG expression. IL-6 stimulation of PLG resulted in a 2.5-fold increase in its transcription. This is also true for the PLG gene of a case with dysplasminogenemia. Although the patient's gene had six mutations in the 5'-flanking region, its promoter activity was 1.8-fold that of normal PLG.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Carcinoma, Hepatocellular
  • Cell Line
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Fibroblasts
  • Gene Library
  • Genes, Reporter
  • Genetic Variation*
  • Genetic Vectors
  • Humans
  • Interleukin-6 / pharmacology*
  • Kinetics
  • Liver Neoplasms
  • Plasminogen / biosynthesis*
  • Plasminogen / genetics*
  • Recombinant Proteins / biosynthesis
  • Regulatory Sequences, Nucleic Acid*
  • Transcription, Genetic / drug effects*
  • Transfection
  • beta-Galactosidase / biosynthesis

Substances

  • Interleukin-6
  • Recombinant Proteins
  • Plasminogen
  • Chloramphenicol O-Acetyltransferase
  • beta-Galactosidase