Simonin F, Gavériaux-Ruff C, Befort K, Matthes H, Lannes B, Micheletti G, Mattéi M G, Charron G, Bloch B, Kieffer B
Ecole Supérieure de Biotechnologie, Parc d'innovation, Boulevard Sébastien Brandt, Illkirch-Graffenstaden, France.
Proc Natl Acad Sci U S A. 1995 Jul 18;92(15):7006-10. doi: 10.1073/pnas.92.15.7006.
Using the mouse delta-opioid receptor cDNA as a probe, we have isolated genomic clones encoding the human mu- and kappa-opioid receptor genes. Their organization appears similar to that of the human delta receptor gene, with exon-intron boundaries located after putative transmembrane domains 1 and 4. The kappa gene was mapped at position q11-12 in human chromosome 8. A full-length cDNA encoding the human kappa-opioid receptor has been isolated. The cloned receptor expressed in COS cells presents a typical kappa 1 pharmacological profile and is negatively coupled to adenylate cyclase. The expression of kappa-opioid receptor mRNA in human brain, as estimated by reverse transcription-polymerase chain reaction, is consistent with the involvement of kappa-opioid receptors in pain perception, neuroendocrine physiology, affective behavior, and cognition. In situ hybridization studies performed on human fetal spinal cord demonstrate the presence of the transcript specifically in lamina II of the dorsal horn. Some divergences in structural, pharmacological, and anatomical properties are noted between the cloned human and rodent receptors.
我们以小鼠δ阿片受体cDNA作为探针,分离出了编码人μ阿片受体和κ阿片受体基因的基因组克隆。它们的结构组织似乎与人δ受体基因相似,外显子-内含子边界位于假定的跨膜结构域1和4之后。κ基因定位于人染色体8的q11-12位置。已分离出编码人κ阿片受体的全长cDNA。在COS细胞中表达的克隆受体呈现典型的κ1药理学特征,并且与腺苷酸环化酶负偶联。通过逆转录-聚合酶链反应估计,κ阿片受体mRNA在人脑中的表达与κ阿片受体参与痛觉、神经内分泌生理学、情感行为和认知过程一致。对人胎儿脊髓进行的原位杂交研究表明,该转录本特异性存在于背角的Ⅱ层。在克隆的人源和啮齿动物受体之间,在结构、药理学和解剖学特性上存在一些差异。