Department of Neurology, University of California, San Francisco, CA 94143.
Department of Neurology, University of California, San Francisco, CA 94143;
Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):3434-3439. doi: 10.1073/pnas.1801693115. Epub 2018 Mar 12.
Adequate sleep is essential for physical and mental health. We previously identified a missense mutation in the human gene () leading to the familial natural short sleep behavioral trait. DEC2 is a transcription factor regulating the circadian clock in mammals, although its role in sleep regulation has been unclear. Here we report that , also known as (), gene expression is increased in the mouse model expressing the mutant h transgene (h). encodes a precursor protein of a neuropeptide producing orexin A and B (hcrt1 and hcrt2), which is enriched in the hypothalamus and regulates maintenance of arousal. In cell culture, DEC2 suppressed () expression through -acting E-box elements. The mutant DEC2 has less repressor activity than WT-DEC2, resulting in increased orexin expression. DEC2-binding affinity for the gene promoter is decreased by the P384R mutation, likely due to weakened interaction with other transcription factors. In vivo, the decreased immobility time of the mutant transgenic mice is attenuated by an orexin receptor antagonist. Our results suggested that DEC2 regulates sleep/wake duration, at least in part, by modulating the neuropeptide hormone orexin.
充足的睡眠对身心健康至关重要。我们之前发现了人类基因中的一个错义突变,导致家族性自然短睡眠行为特征。DEC2 是一种调节哺乳动物生物钟的转录因子,但其在睡眠调节中的作用尚不清楚。在这里,我们报告说,也被称为 (),在表达突变 h 转基因 (h) 的小鼠模型中,基因表达增加。编码一种产生食欲素 A 和 B (hcrt1 和 hcrt2) 的神经肽前体蛋白,它在下丘脑富集并调节觉醒的维持。在细胞培养中,DEC2 通过 -作用 E 盒元件抑制 () 表达。突变型 DEC2 的抑制活性比 WT-DEC2 低,导致食欲素表达增加。突变型 DEC2 与基因启动子的结合亲和力降低,可能是由于与其他转录因子的相互作用减弱。在体内,通过使用一种食欲素受体拮抗剂可以减弱突变型转基因小鼠的不动时间减少。我们的结果表明,DEC2 通过调节神经肽激素食欲素来调节睡眠/觉醒持续时间,至少部分如此。