Wang J B, Johnson P S, Persico A M, Hawkins A L, Griffin C A, Uhl G R
Molecular Neurobiology Branch, NIDA, Baltimore, MD 21224.
FEBS Lett. 1994 Jan 31;338(2):217-22. doi: 10.1016/0014-5793(94)80368-4.
A human mu opiate receptor cDNA has been identified from a cerebral cortical cDNA library using sequences from the rat mu opiate receptor cDNA. The human mu opiate receptor (h mu OR1) shares 95% amino acid identity with the rat sequence. The expressed mu OR1 recognized tested opiate drugs and opioid peptides in a sodium- and GTP-sensitive fashion with affinities virtually identical to those displayed by the rat mu opiate receptor. Effects on cyclic AMP are similar to those noted for the rat mu opiate receptor. An 18 kb genomic clone hybridizing with the h mu OR1 cDNA contains 63 and 489 bp exonic sequences flanked by splice donor/acceptor sequences. Analysis of hybridization to DNA prepared from human rodent hybrid cell lines and chromosomal in situ hybridization studies indicate localization to 6q24-25. An MspI polymorphism, producing a 3.7 kb band, may prove useful in assessing this gene's involvement in neuropsychiatric disorders involving opiatergic systems.
利用大鼠μ阿片受体cDNA的序列,从大脑皮质cDNA文库中鉴定出了人类μ阿片受体cDNA。人类μ阿片受体(hμOR1)与大鼠序列具有95%的氨基酸同一性。表达的μOR1以对钠和GTP敏感的方式识别受试阿片类药物和阿片样肽,其亲和力与大鼠μ阿片受体几乎相同。对环磷酸腺苷的影响与大鼠μ阿片受体的相似。一个与hμOR1 cDNA杂交的18kb基因组克隆包含63和489bp的外显子序列,两侧为剪接供体/受体序列。对从人鼠杂交细胞系制备的DNA的杂交分析和染色体原位杂交研究表明该基因定位于6q24 - 25。产生3.