Chen H, Charlat O, Tartaglia L A, Woolf E A, Weng X, Ellis S J, Lakey N D, Culpepper J, Moore K J, Breitbart R E, Duyk G M, Tepper R I, Morgenstern J P
Millennium Pharmaceuticals, Incorporated, Cambridge, Massachusetts 02139, USA.
Cell. 1996 Feb 9;84(3):491-5. doi: 10.1016/s0092-8674(00)81294-5.
OB-R is a high affinity receptor for leptin, an important circulating signal for the regulation of body weight. We identified an alternatively spliced transcript that encodes a form of mouse OB-R with a long intracellular domain. db/db mice also produce this alternatively spliced transcript, but with a 106 nt insertion that prematurely terminates the intracellular domain. We further identified G --> T point mutation in the genomic OB-R sequence in db/db mice. This mutation generates a donor splice site that converts the 106 nt region to a novel exon retained in the OB-R transcript. We predict that the long intracellular domain form of OB-R is crucial for initiating intracellular signal transduction, and as a corollary, the inability to produce this form of OB-R leads to the severe obese phenotype found in db/db mice.
OB-R是瘦素的高亲和力受体,瘦素是调节体重的重要循环信号。我们鉴定出一种可变剪接转录本,其编码一种具有长胞内结构域的小鼠OB-R形式。db/db小鼠也产生这种可变剪接转录本,但有一个106 nt的插入片段,该片段使胞内结构域过早终止。我们进一步在db/db小鼠的基因组OB-R序列中鉴定出G→T点突变。该突变产生一个供体剪接位点,将106 nt区域转化为保留在OB-R转录本中的一个新外显子。我们预测,OB-R的长胞内结构域形式对于启动胞内信号转导至关重要,相应地,无法产生这种形式的OB-R会导致db/db小鼠出现严重肥胖表型。