Molecular cloning and expression of human prostacyclin synthase

Biochem Biophys Res Commun. 1994 May 16;200(3):1728-34. doi: 10.1006/bbrc.1994.1652.

Abstract

The cDNA for human prostacyclin synthase was cloned by polymerase chain reaction using poly(A)+ RNA from human aortic endothelial cells according to the partial nucleotide sequence of prostacyclin synthase gene. The cloned cDNA with a size of 1977 base pairs contained a 1500 base pairs open reading frame which encoded a 500 amino acid protein sharing an 88% identity with bovine prostacyclin synthase. RNA blot analysis indicated that the size of major prostacyclin synthase mRNA of human aortic endothelial cells was approximately 6 kilobases and that its mRNA level was increased by interleukin 1 or interleukin 6 treatment. Moreover, tissue distribution study demonstrated that prostacyclin synthase mRNA is widely expressed in human tissues and is particularly abundant in ovary, heart, skeletal muscle, lung, and prostate. These results suggest a variety of physiological roles of prostacyclin in addition to the implications in the cardiovascular system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cloning, Molecular
  • Cytochrome P-450 Enzyme System / genetics*
  • DNA Primers / chemistry
  • DNA, Complementary / genetics
  • Endothelium, Vascular
  • Gene Expression
  • Humans
  • Intramolecular Oxidoreductases*
  • Isomerases / genetics*
  • Molecular Sequence Data
  • RNA, Messenger / genetics
  • Restriction Mapping

Substances

  • DNA Primers
  • DNA, Complementary
  • RNA, Messenger
  • Cytochrome P-450 Enzyme System
  • Isomerases
  • Intramolecular Oxidoreductases
  • prostacyclin synthetase

Associated data

  • GENBANK/D38145