Lee G H, Proenca R, Montez J M, Carroll K M, Darvishzadeh J G, Lee J I, Friedman J M
Howard Hughes Medical Institute, Rockefeller University, New York, New York 10021, USA.
Nature. 1996 Feb 15;379(6566):632-5. doi: 10.1038/379632a0.
Mutations in the mouse diabetes (db) gene result in obesity and diabetes in a syndrome resembling morbid human obesity. Previous data suggest that the db gene encodes the receptor for the obese (ob) gene product, leptin. A leptin receptor was recently cloned from choroid plexus and shown to map to the same 6-cM interval on mouse chromosome 4 as db. This receptor maps to the same 300-kilobase interval as db, and has at least six alternatively spliced forms. One of these splice variants is expressed at a high level in the hypothalamus, and is abnormally spliced in C57BL/Ks db/db mice. The mutant protein is missing the cytoplasmic region, and is likely to be defective in signal transduction. This suggests that the weight-reducing effects of leptin may be mediated by signal transduction through a leptin receptor in the hypothalamus.
小鼠糖尿病(db)基因的突变会导致肥胖和糖尿病,其症状类似于人类的病态肥胖。先前的数据表明,db基因编码肥胖(ob)基因产物瘦素的受体。最近从脉络丛中克隆出一种瘦素受体,并且显示它在小鼠4号染色体上与db基因位于相同的6厘摩区间内。该受体与db基因位于相同的300千碱基区间内,并且至少有六种可变剪接形式。其中一种剪接变体在下丘脑中高水平表达,并且在C57BL/Ks db/db小鼠中发生异常剪接。突变蛋白缺失细胞质区域,可能在信号转导方面存在缺陷。这表明瘦素的减重作用可能是通过下丘脑的瘦素受体进行信号转导来介导的。