Debruyne Jason P, Noton Elizabeth, Lambert Christopher M, Maywood Elizabeth S, Weaver David R, Reppert Steven M
Department of Neurobiology, University of Massachusetts Medical School, 364 Plantation Street, Worcester, Massachusetts 01605, USA.
Neuron. 2006 May 4;50(3):465-77. doi: 10.1016/j.neuron.2006.03.041.
The circadian clock mechanism in the mouse is composed of interlocking transcriptional feedback loops. Two transcription factors, CLOCK and BMAL1, are believed to be essential components of the circadian clock. We have used the Cre-LoxP system to generate whole-animal knockouts of CLOCK and evaluated the resultant circadian phenotypes. Surprisingly, CLOCK-deficient mice continue to express robust circadian rhythms in locomotor activity, although they do have altered responses to light. At the molecular and biochemical levels, clock gene mRNA and protein levels in both the master clock in the suprachiasmatic nuclei and a peripheral clock in the liver show alterations in the CLOCK-deficient animals, although the molecular feedback loops continue to function. Our data challenge a central feature of the current mammalian circadian clock model regarding the necessity of CLOCK:BMAL1 heterodimers for clock function.
小鼠体内的昼夜节律时钟机制由相互连锁的转录反馈环组成。两种转录因子,即CLOCK和BMAL1,被认为是昼夜节律时钟的重要组成部分。我们利用Cre-LoxP系统构建了CLOCK的全动物敲除模型,并评估了由此产生的昼夜节律表型。令人惊讶的是,CLOCK基因敲除小鼠的运动活动仍表现出强劲的昼夜节律,尽管它们对光的反应有所改变。在分子和生化水平上,视交叉上核中的主时钟和肝脏中的外周时钟内的时钟基因mRNA和蛋白质水平在CLOCK基因敲除动物中均显示出变化,尽管分子反馈环仍在发挥作用。我们的数据对当前哺乳动物昼夜节律时钟模型中关于CLOCK:BMAL1异二聚体对时钟功能必要性的核心特征提出了挑战。