Molecular cloning of a non-isopeptide-selective human endothelin receptor

Biochem Biophys Res Commun. 1991 Jul 15;178(1):248-55. doi: 10.1016/0006-291x(91)91806-n.

Abstract

We isolated several complementary DNA (cDNA) clones encoding a non-isopeptide-selective human endothelin receptor (ETBR) from a human placenta cDNA library. The clones, different in the length of their 3'-untranslated regions, encoded the same 442-amino acid protein with a transmembrane topology similar to that of other G protein-coupled receptors. The rank order of the binding of ET isopeptides (ET-1, ET-2 and ET-3) to the receptor expressed in COS-7 cells was ET-1 = ET-2 = ET-3. Northern blot analysis identified three mRNA species, 4.3 kb, 2.7 kb and 1.7 kb in size, probably generated by their use of alternative polyadenylation sites. These mRNAs were expressed in a wide variety of human tissues, at the highest level in the brain and at a significant level in cultured endothelial cells.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cell Line
  • Cloning, Molecular / methods
  • DNA / genetics
  • DNA / isolation & purification
  • Endothelins / metabolism
  • Female
  • Gene Library
  • Humans
  • Kinetics
  • Molecular Sequence Data
  • Organ Specificity
  • Placenta / physiology
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / isolation & purification
  • Rats
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / metabolism
  • Receptors, Endothelin
  • Recombinant Proteins / metabolism
  • Restriction Mapping
  • Sequence Homology, Nucleic Acid
  • Transfection

Substances

  • Endothelins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Endothelin
  • Recombinant Proteins
  • DNA