Lok S, Kuijper J L, Jelinek L J, Kramer J M, Whitmore T E, Sprecher C A, Mathewes S, Grant F J, Biggs S H, Rosenberg G B
Department of Molecular and Cellular Biology, ZymoGenetics Inc., Seattle, WA 95105.
Gene. 1994 Mar 25;140(2):203-9. doi: 10.1016/0378-1119(94)90545-2.
Characterization of the human glucagon-receptor-encoding gene (GGR) should provide a greater understanding of blood glucose regulation and may reveal a genetic basis for the pathogenesis of diabetes. A cDNA encoding a complete functional human glucagon receptor (GGR) was isolated from a liver cDNA library by a combination of polymerase chain reaction and colony hybridization. The cDNA encodes a receptor protein with 80% identity to rat GGR that binds [125I]glucagon and transduces a signal leading to increases in the concentration of intracellular cyclic adenosine 3',5'-monophosphate. Southern blot analysis of human DNA reveals a hybridization pattern consistent with a single GGR locus. In situ hybridization to metaphase chromosome preparations maps the GGR locus to chromosome 17q25. Analysis of the genomic sequence shows that the coding region spans over 5.5 kb and is interrupted by 12 introns.
对人类胰高血糖素受体编码基因(GGR)的特性进行研究,有助于更深入地了解血糖调节机制,并可能揭示糖尿病发病机制的遗传基础。通过聚合酶链反应和菌落杂交相结合的方法,从肝脏cDNA文库中分离出了编码完整功能性人类胰高血糖素受体(GGR)的cDNA。该cDNA编码的受体蛋白与大鼠GGR有80%的同源性,能结合[125I]胰高血糖素并转导信号,导致细胞内3',5'-环磷酸腺苷浓度升高。对人类DNA的Southern印迹分析显示,杂交模式与单一GGR基因座一致。对中期染色体标本进行原位杂交,将GGR基因座定位到17号染色体q25区域。基因组序列分析表明,编码区跨度超过5.5 kb,被12个内含子打断。