Gubitz A K, Reppert S M
Pediatric Service, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, 02114, USA.
Genomics. 1999 Jan 15;55(2):248-51. doi: 10.1006/geno.1998.5661.
Recent efforts to clone further members of the melatonin receptor family have led to the identification of a novel G-protein-coupled receptor in human pituitary. This receptor, referred to as H9, is clearly related to high-affinity melatonin receptors yet unable to bind this hormone. We now report the cloning and expression of the cDNA encoding the H9 receptor in mice. The mouse clone encodes a protein of 591 amino acids that shares 74% amino acid identity with the human receptor and is unable to bind 2-[125I]iodomelatonin when transiently expressed in COS-7 cells. We also determined the chromosome loci of the human and mouse H9 receptor genes. Both genes were found to be X-linked: radiation hybrid mapping revealed that the human H9 gene (GPR50) is localized to Xq28. The mouse gene (Gpr50) was determined to lie in the proximal portion of chromosome X by means of interspecific backcross analysis. These loci might be relevant to genetically based neuroendocrine disorders.
近期为克隆褪黑素受体家族的更多成员所做的努力,已促成在人垂体中鉴定出一种新型G蛋白偶联受体。这种受体被称为H9,它显然与高亲和力褪黑素受体相关,但无法结合该激素。我们现在报告编码小鼠H9受体的cDNA的克隆及表达情况。小鼠克隆体编码一种由591个氨基酸组成的蛋白质,该蛋白质与人类受体有74%的氨基酸同一性,并且在COS-7细胞中瞬时表达时无法结合2-[¹²⁵I]碘褪黑素。我们还确定了人类和小鼠H9受体基因的染色体定位。发现这两个基因均与X染色体连锁:辐射杂种图谱分析表明,人类H9基因(GPR50)定位于Xq28。通过种间回交分析确定小鼠基因(Gpr50)位于X染色体的近端部分。这些基因座可能与基于遗传的神经内分泌疾病有关。