CIPC is a mammalian circadian clock protein without invertebrate homologues

被引:61
作者
Zhao, Wen-Ning
Malinin, Nikolay
Yang, Fu-Chia
Staknis, David
Gekakis, Nicholas
Maier, Bert
Reischl, Silke
Kramer, Achim
Weitz, Charles J.
机构
[1] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[2] Charite Univ Med Berlin, Lab Chronobiol, Inst Med Immunol, D-10098 Berlin, Germany
关键词
D O I
10.1038/ncb1539
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
At the core of the mammalian circadian clock is a feedback loop in which the heterodimeric transcription factor CLOCK-Brain, Muscle Arnt-like-1 (BMAL1) drives expression of its negative regulators, periods (PERs) and cryptochromes (CRYs). Here, we provide evidence that CLOCK-Interacting Protein, Circadian ( CIPC) is an additional negative-feedback regulator of the circadian clock. CIPC exhibits circadian regulation in multiple tissues, and it is a potent and specific inhibitor of CLOCK-BMAL1 activity that functions independently of CRYs. CIPC-CLOCK protein complexes are present in vivo, and depletion of endogenous CIPC shortens the circadian period length. CIPC is unrelated to known proteins and has no recognizable homologues outside vertebrates. Our results suggest that negative feedback in the mammalian circadian clock is divided into distinct pathways, and that the addition of new genes has contributed to the complexity of vertebrate clocks.
引用
收藏
页码:268 / U53
页数:23
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