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.
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Authors | R Janssens, D Communi, S Pirotton, M Samson, M Parmentier, J M Boeynaems |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 221
Issue 3
Pg. 588-93
(Apr 25 1996)
ISSN: 0006-291X [Print] United States |
PMID | 8630005
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- P2RY1 protein, human
- P2ry1 protein, mouse
- Receptors, Purinergic P2
- Receptors, Purinergic P2Y1
- DNA
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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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