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Molecular cloning and characterization of the mouse P2Y4 nucleotide receptor.

机译:小鼠P2Y4核苷酸受体的分子克隆和表征。

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摘要

To isolate the mouse P2Y4 receptor gene, a mouse genomic library was screened with a human P2Y4 probe. An open reading frame encoding a protein of 361 amino acids was isolated. This protein showed 82% and 95% amino acid identity with the human and rat P2Y4 receptors, respectively. By reverse transcription and polymerase chain reaction (RT-PCR), the P2Y4 messenger RNA was detected in mouse liver, intestine, stomach, bladder and lung among the 16 mouse tissues tested. In 1321N1 transfected cells, the mouse P2Y4 receptor was equally activated by UTP and ATP, and was antagonized by pyridoxal-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS) and Reactive Blue 2, and not by suramin. Moreover, when expressed in 1321N1 cells, the rat P2Y4 is also antagonized by PPADS. Thus, when compared in the same expression system, the mouse P2Y4 is closer to the rat ortholog in terms of agonist stimulation, while in terms of antagonist profile, the three P2Y4 receptor orthologs are similar.
机译:为了分离小鼠P2Y4受体基因,用人类P2Y4探针筛选了小鼠基因组文库。分离出编码361个氨基酸的蛋白质的开放阅读框。该蛋白分别与人和大鼠P2Y4受体显示82%和95%的氨基酸同一性。通过逆转录和聚合酶链反应(RT-PCR),在测试的16种小鼠组织中的小鼠肝,肠,胃,膀胱和肺中检测到P2Y4信使RNA。在1321N1转染的细胞中,小鼠P2Y4受体同样被UTP和ATP激活,并被吡al醛-磷酸-6-偶氮苯基-2',4'-二磺酸(PPADS)和活性蓝2拮抗,而不是由苏拉明拮抗。而且,当在1321N1细胞中表达时,PPADS也拮抗大鼠P2Y4。因此,当在同一表达系统中比较时,小鼠P2Y4在激动剂刺激方面更接近大鼠直系同源物,而就拮抗剂谱而言,这三种P2Y4受体直系同源物相似。

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