Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Elife. 2021 Dec 13;10:e69773. doi: 10.7554/eLife.69773.
In the mouse, () expression in tissues peripheral to the suprachiasmatic nuclei (SCN) increases during sleep deprivation and at times of the day when animals are predominantly awake spontaneously, suggesting that the circadian sleep-wake distribution directly contributes to the daily rhythms in . We found support for this hypothesis by recording sleep-wake state alongside PER2 bioluminescence in freely behaving mice, demonstrating that PER2 bioluminescence increases during spontaneous waking and decreases during sleep. The temporary reinstatement of PER2-bioluminescence rhythmicity in behaviorally arrhythmic SCN-lesioned mice submitted to daily recurring sleep deprivations substantiates our hypothesis. Mathematical modeling revealed that PER2 dynamics can be described by a damped harmonic oscillator driven by two forces: a sleep-wake-dependent force and an SCN-independent circadian force. Our work underscores the notion that in peripheral tissues the clock gene circuitry integrates sleep-wake information and could thereby contribute to behavioral adaptability to respond to homeostatic requirements.
在小鼠中,()在视交叉上核(SCN)周围组织中的表达在睡眠剥夺期间以及动物主要自发清醒的白天时间增加,表明昼夜睡眠-觉醒分布直接导致()的每日节律。我们通过在自由活动的小鼠中记录睡眠-觉醒状态和 PER2 生物发光来支持这一假设,证明 PER2 生物发光在自发清醒期间增加,在睡眠期间减少。在接受每日反复睡眠剥夺的行为节律紊乱 SCN 损伤小鼠中,PER2 生物发光节律性的暂时恢复证实了我们的假设。数学模型表明,PER2 动力学可以用两个力驱动的阻尼谐波振荡器来描述:睡眠-觉醒依赖性力和 SCN 独立的昼夜力。我们的工作强调了这样一种观点,即在周围组织中,时钟基因电路整合了睡眠-觉醒信息,并因此有助于行为适应性以响应稳态需求。