Small molecule modifiers of circadian clocks

被引:103
作者
Chen, Zheng [1 ]
Yoo, Seung-Hee [2 ]
Takahashi, Joseph S. [2 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
Metabolites; Synthetic compounds; Period; Phase; Amplitude; Clock-associated diseases; Chronotherapy; REV-ERB-ALPHA; GENE-EXPRESSION; LIGAND-BINDING; DNA-DAMAGE; CRYSTAL-STRUCTURE; CHEMICAL BIOLOGY; METABOLIC CYCLE; CORE COMPONENT; PHASE DELAYS; REDOX STATE;
D O I
10.1007/s00018-012-1207-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Circadian clocks orchestrate 24-h oscillations of essential physiological and behavioral processes in response to daily environmental changes. These clocks are remarkably precise under constant conditions yet highly responsive to resetting signals. With the molecular composition of the core oscillator largely established, recent research has increasingly focused on clock-modifying mechanisms/molecules. In particular, small molecule modifiers, intrinsic or extrinsic, are emerging as powerful tools for understanding basic clock biology as well as developing putative therapeutic agents for clock-associated diseases. In this review, we will focus on synthetic compounds capable of modifying the period, phase, or amplitude of circadian clocks, with particular emphasis on the mammalian clock. We will discuss the potential of exploiting these small molecule modifiers in both basic and translational research.
引用
收藏
页码:2985 / 2998
页数:14
相关论文
共 164 条
[1]
Akashi M, 2000, GENE DEV, V14, P645
[2]
Vascular Disease in Mice With a Dysfunctional Circadian Clock [J].
Anea, Ciprian B. ;
Zhang, Maoxiang ;
Stepp, David W. ;
Simkins, G. Bryan ;
Reed, Guy ;
Fulton, David J. ;
Rudic, R. Daniel .
CIRCULATION, 2009, 119 (11) :1510-U88
[3]
[Anonymous], J HYDRO ENVIRON RES
[4]
Functional identification of the mouse circadian Clock gene by transgenic BAC rescue [J].
Antoch, MP ;
Song, EJ ;
Chang, AM ;
Vitaterna, MH ;
Zhao, YL ;
Wilsbacher, LD ;
Sangoram, AM ;
King, DP ;
Pinto, LH ;
Takahashi, JS .
CELL, 1997, 89 (04) :655-667
[5]
Shift work: coping with the biological clock [J].
Arendt, Josephine .
OCCUPATIONAL MEDICINE-OXFORD, 2010, 60 (01) :10-20
[6]
An inhibitor of casein kinase 1 ε/δ partially normalizes the manic-like behaviors of the ClockΔ19 mouse [J].
Arey, Rachel ;
McClung, Colleen A. .
BEHAVIOURAL PHARMACOLOGY, 2012, 23 (04) :392-396
[7]
SIRT1 regulates circadian clock gene expression through PER2 deacetylation [J].
Asher, Gad ;
Gatfield, David ;
Stratmann, Markus ;
Reinke, Hans ;
Dibner, Charna ;
Kreppel, Florian ;
Mostoslavsky, Raul ;
Alt, Frederick W. ;
Schibler, Ueli .
CELL, 2008, 134 (02) :317-328
[8]
Crosstalk between Components of Circadian and Metabolic Cycles in Mammals [J].
Asher, Gad ;
Schibler, Ueli .
CELL METABOLISM, 2011, 13 (02) :125-137
[9]
Poly(ADP-Ribose) Polymerase 1 Participates in the Phase Entrainment of Circadian Clocks to Feeding [J].
Asher, Gad ;
Reinke, Hans ;
Altmeyer, Matthias ;
Gutierrez-Arcelus, Maria ;
Hottiger, Michael O. ;
Schibler, Ueli .
CELL, 2010, 142 (06) :943-953
[10]
An inhibitor of casein kinase Iε induces phase delays in circadian rhythms under free-running and entrained conditions [J].
Badura, Lori ;
Swanson, Terri ;
Adamowicz, Wendy ;
Adams, Jessica ;
Cianfrogna, Julie ;
Fisher, Katherine ;
Holland, Janice ;
Kleiman, Robin ;
Nelson, Frederick ;
Reynolds, Linda ;
Germain, Kristin St. ;
Schaeffer, Eric ;
Tate, Barbara ;
Sprouse, Jeffrey .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 322 (02) :730-738