Abnormal splicing of the leptin receptor in diabetic mice

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 t...

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Veröffentlicht in:Nature (London) 1996-02, Vol.379 (6566), p.632-635
Hauptverfasser: Lee, G.H, Proenca, R, Montez, J.M, Carroll, K.M, Darvishzadeh, J.G, Lee, J.I, Friedman, J.M
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Sprache:eng
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Zusammenfassung: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.
ISSN:0028-0836
1476-4687
DOI:10.1038/379632a0