Iismaa T P, Kiefer J, Liu M L, Baker E, Sutherland G R, Shine J
Garvan Institute of Medical Research, St. Vincent's Hospital, Sydney, New South Wales, Australia.
Genomics. 1994 Nov 15;24(2):391-4. doi: 10.1006/geno.1994.1635.
Degenerate oligonucleotide primers designed against known G-protein-coupled receptors were used in polymerase chain reaction amplification to isolate a novel receptor sequence (R4) from a rat insulinoma cell line and its human homolog (GPR3) from a human neuroblastoma cDNA library. The novel human receptor sequence is expressed in low abundance predominantly in the central nervous system and at low levels in the lung and kidney. The gene encoding GPR3 is intronless within the coding region, contains at least one intron in the 5'-untranslated region, and has been localized to chromosome 1p34.3. The activating ligand for the homologous receptors R4 and GPR3 is not known, but sequence similarity with the closely related orphan rat receptor R334 [FEBS Lett. 292:243 (1991)] suggests that R334 and the homologous receptors R4 and GPR3 probably represent two discrete molecular subtypes that interact with the same or closely related ligands.
针对已知G蛋白偶联受体设计的简并寡核苷酸引物用于聚合酶链反应扩增,以从大鼠胰岛素瘤细胞系中分离出一种新的受体序列(R4),并从人神经母细胞瘤cDNA文库中分离出其人类同源物(GPR3)。这种新的人类受体序列表达丰度较低,主要存在于中枢神经系统,在肺和肾中表达水平较低。编码GPR3的基因在编码区内无内含子,在5'-非翻译区内至少有一个内含子,并且已定位到染色体1p34.3。同源受体R4和GPR3的激活配体尚不清楚,但与密切相关的孤儿大鼠受体R334 [《欧洲生物化学学会联合会快报》292:243(1991)] 的序列相似性表明,R334以及同源受体R4和GPR3可能代表与相同或密切相关配体相互作用的两种不同分子亚型。