Abnormal splicing of the leptin receptor in diabetic mice

被引:2006
作者
Lee, GH [1 ]
Proenca, R [1 ]
Montez, JM [1 ]
Carroll, KM [1 ]
Darvishzadeh, JG [1 ]
Lee, JI [1 ]
Friedman, JM [1 ]
机构
[1] ROCKEFELLER UNIV, DEPT MOLEC GENET, NEW YORK, NY 10021 USA
关键词
D O I
10.1038/379632a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MUTATIONS in the mouse diabetes (db) gene result in obesity and diabetes in a syndrome resembling morbid human obesity(1), Previous data suggest that the db gene encodes the receptor for the obese (ob) gene product, leptin(2-7). 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(8). 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.
引用
收藏
页码:632 / 635
页数:4
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