A clock shock: Mouse CLOCK is not required for circadian oscillator function

被引:329
作者
DeBruyne, Jason P.
Noton, Elizabeth
Lambert, Christopher M.
Maywood, Elizabeth S.
Weaver, David R.
Reppert, Steven M.
机构
[1] Univ Massachusetts, Sch Med, Dept Neurobiol, Worcester, MA 01605 USA
[2] MRC, Mol Biol Lab, Div Neurobiol, Cambridge CB2 2QH, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.neuron.2006.03.041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:465 / 477
页数:13
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