Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):1851-5. doi: 10.1073/pnas.92.6.1851.

Abstract

Increased plasminogen-activator inhibitor 1 (PAI-1) activity is a common finding in patients with coronary heart disease. Here we provide evidence for an independent, etiological role of PAI-1 in myocardial infarction. The 4G allele of a recently described common 4/5-guanine-tract (4G/5G) polymorphism in the PAI-1 promoter is associated with higher plasma PAI-1 activity. The prevalence of the 4G allele is significantly higher in patients with myocardial infarction before the age of 45 than in population-based controls (allele frequencies of 0.63 vs. 0.53). Both alleles bind a transcriptional activator, whereas the 5G allele also binds a repressor protein to an overlapping binding site. In the absence of bound repressor, the basal level of PAI-1 transcription is increased.

Publication types

  • Clinical Trial
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Base Sequence
  • Binding Sites
  • Carcinoma, Hepatocellular
  • Cell Line
  • Cell Nucleus / metabolism
  • DNA-Binding Proteins / metabolism
  • Deoxyribonuclease I
  • Gene Expression*
  • Genotype
  • Humans
  • Liver Neoplasms
  • Male
  • Methylation
  • Molecular Sequence Data
  • Myocardial Infarction / genetics*
  • Myocardial Infarction / metabolism
  • Odds Ratio
  • Plasminogen Activator Inhibitor 1 / biosynthesis*
  • Plasminogen Activator Inhibitor 1 / genetics*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic*
  • Reference Values
  • Transcription, Genetic*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • DNA-Binding Proteins
  • Plasminogen Activator Inhibitor 1
  • Deoxyribonuclease I