A functional genomics strategy reveals rora as a component of the mammalian circadian clock

被引:851
作者
Sato, TK
Panda, S
Miraglia, LJ
Reyes, TM
Rudic, RD
McNamara, P
Naik, KA
Fitzgerald, GA
Kay, SA
Hogenesch, JB
机构
[1] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
[2] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[4] Lab Neuronal Struct, La Jolla, CA 92037 USA
[5] Funct Salk Inst, La Jolla, CA 92037 USA
[6] Univ Penn, Sch Med, Ctr Expt Therapeut, Philadelphia, PA 19104 USA
[7] Phenomix Corp, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.neuron.2004.07.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mammalian circadian clock plays an integral role in timing rhythmic physiology and behavior, such as locomotor activity, with anticipated daily environmental changes. The master oscillator resides within the suprachiasmatic nucleus (SCN), which can maintain circadian rhythms in the absence of synchronizing light input. Here, we describe a genomics-based approach to identify circadian activators of Bmal1, itself a key transcriptional activator that is necessary for core oscillator function. Using cell-based functional assays, as well as behavioral and molecular analyses, we identified Rora as an activator of Bmal1 transcription within the SCN. Rora is required for normal Bmal1 expression and consolidation of daily locomotor activity and is regulated by the core clock in the SCN. These results suggest that opposing activities of the orphan nuclear receptors Rora and Rev-erb alpha, which represses Bmal1 expression, are important in the maintenance of circadian clock function.
引用
收藏
页码:527 / 537
页数:11
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