Functional study of the germinal angiotensin I-converting enzyme promoter

Biochem Biophys Res Commun. 1992 Nov 30;189(1):134-40. doi: 10.1016/0006-291x(92)91535-x.

Abstract

Polymerase chain amplification experiments indicate that the germinal specific promoter of the angiotensin I-converting enzyme (ACE) is completely extinguished in somatic tissues. Despite this very strict specificity of expression, the germinal ACE promoter is active in transient transfection experiments in two somatic cell lines and one cell line of germinal origin. The analysis of the promoter shows the existence two regulatory elements within the first 350 bp: a proximal positive element and a distal negative element.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cathepsin C
  • Cell Line
  • Chloramphenicol O-Acetyltransferase / genetics
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Cloning, Molecular
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / genetics*
  • Exons
  • Female
  • Humans
  • Introns
  • Luciferases / genetics
  • Luciferases / metabolism
  • Male
  • Mice
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides
  • Organ Specificity
  • Ovary / enzymology*
  • Peptidyl-Dipeptidase A / genetics*
  • Plasmids
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic*
  • RNA / genetics
  • RNA / isolation & purification
  • Regulatory Sequences, Nucleic Acid
  • Testis / enzymology*

Substances

  • Oligodeoxyribonucleotides
  • Colforsin
  • RNA
  • Cyclic AMP
  • Luciferases
  • Chloramphenicol O-Acetyltransferase
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
  • Cathepsin C
  • Peptidyl-Dipeptidase A