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Cloning and tissue distribution of the human P2Y1 receptor.

Abstract
Sets of degenerate oligonucleotide primers synthesized on the basis of the best conserved regions of the chick brain P2Y/P2Y1 and the murine neuroblastoma P2U/P2Y2 receptors were used in polymerase chain reaction experiments on human genomic DNA. An amplified fragment of 712 base pairs was then used as a probe to screen a human genomic DNA library. Several clones were isolated and sequencing revealed an intronless 1122 base pair open reading frame. The corresponding amino acid sequence revealed 83% identity with the chick brain P2Y1 receptor and 34% with the murine neuroblastoma P2Y2 receptor. In COS-7 cells transfected with the coding sequence inserted into the pcDNA3 expression vector, 2-methylthioATP and ATP produced a strong stimulation of inositol phosphates, a typical response of a P2Y1 receptor. Northern blot analysis detected a 6.7 kilobase messenger RNA in most human tissues, the strongest signals being observed in prostate and ovary.
AuthorsR Janssens, D Communi, S Pirotton, M Samson, M Parmentier, J M Boeynaems
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 221 Issue 3 Pg. 588-93 (Apr 25 1996) ISSN: 0006-291X [Print] United States
PMID8630005 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • P2RY1 protein, human
  • P2ry1 protein, mouse
  • Receptors, Purinergic P2
  • Receptors, Purinergic P2Y1
  • DNA
Topics
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cell Line
  • Chickens
  • Cloning, Molecular
  • DNA
  • Humans
  • Mice
  • Molecular Sequence Data
  • Receptors, Purinergic P2 (genetics, metabolism)
  • Receptors, Purinergic P2Y1
  • Tissue Distribution
  • Tumor Cells, Cultured

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