Cloning of a G protein-activated inwardly rectifying potassium channel from human cerebellum

  • Brain Res Mol Brain Res. 1996 Jul;39(1-2):23-30. doi: 10.1016/0169-328x(95)00349-w.
O Schoots  1 ,  K T Yue ,  J F MacDonald ,  D R Hampson ,  J N Nobrega ,  L M Dixon ,  H H Van Tol
Affiliations
  • 1. Clarke Institute of Psychiatry, Toronto, Ont., Canada.
Abstract

Based on sequence homology with the rat atrial G protein-coupled muscarinic Potassium Channel (GIRK1 or KGA1/KGB1), a human cDNA encoding a G protein-activated inwardly rectifying K+ channel (HGIRK1) was isolated. The cDNA encodes a protein of 501 Amino acids and shares 99% identity to rat GIRK1 in its total amino acid sequence. Southern blot analysis of genomic DNA indicates a high degree of conservation among various species. In the human population a useful NlaIII restriction fragment length polymorphism was found in the coding sequence of HGIRK1. Co-expression of HGIRK1 and the 5-HT1A receptor in Xenopus oocytes resulted in opening of the channel upon treatment with serotonin. HGIRK1 currents showed strong inward rectification and could be blocked by extracellular Ba2+. Northern blot analysis shows that HGIRK1 expression in human is most abundant in the brain, while lower levels are round in kidney and heart.