AMPK Regulates the Circadian Clock by Cryptochrome Phosphorylation and Degradation

被引:693
作者
Lamia, Katja A. [2 ]
Sachdeva, Uma M. [1 ]
DiTacchio, Luciano [3 ]
Williams, Elliot C. [2 ]
Alvarez, Jacqueline G. [2 ,4 ]
Egan, Daniel F. [5 ]
Vasquez, Debbie S. [5 ]
Juguilon, Henry [2 ,4 ]
Panda, Satchidananda [3 ]
Shaw, Reuben J. [4 ,5 ]
Thompson, Craig B. [1 ]
Evans, Ronald M. [2 ,4 ]
机构
[1] Univ Penn, Sch Med, Dept Canc Biol, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Salk Inst Biol Studies, Gene Express Lab, La Jolla, CA 92037 USA
[3] Salk Inst Biol Studies, Regulatory Biol Lab, La Jolla, CA 92037 USA
[4] Salk Inst Biol Studies, Howard Hughes Med Inst, La Jolla, CA 92037 USA
[5] Salk Inst Biol Studies, Mol & Cellular Biol Lab, La Jolla, CA 92037 USA
关键词
ACTIVATED PROTEIN-KINASE; GENE-EXPRESSION; LIVER; OSCILLATORS; BMAL1; FORM;
D O I
10.1126/science.1172156
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Circadian clocks coordinate behavioral and physiological processes with daily light-dark cycles by driving rhythmic transcription of thousands of genes. Whereas the master clock in the brain is set by light, pacemakers in peripheral organs, such as the liver, are reset by food availability, although the setting, or "entrainment," mechanisms remain mysterious. Studying mouse fibroblasts, we demonstrated that the nutrient-responsive adenosine monophosphate-activated protein kinase (AMPK) phosphorylates and destabilizes the clock component cryptochrome 1 (CRY1). In mouse livers, AMPK activity and nuclear localization were rhythmic and inversely correlated with CRY1 nuclear protein abundance. Stimulation of AMPK destabilized cryptochromes and altered circadian rhythms, and mice in which the AMPK pathway was genetically disrupted showed alterations in peripheral clocks. Thus, phosphorylation by AMPK enables cryptochrome to transduce nutrient signals to circadian clocks in mammalian peripheral organs.
引用
收藏
页码:437 / 440
页数:4
相关论文
共 28 条
[1]   AMP-activated protein kinase plays a role in the control of food intake [J].
Andersson, U ;
Filipsson, K ;
Abbott, CR ;
Woods, A ;
Smith, K ;
Bloom, SR ;
Carling, D ;
Small, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :12005-12008
[2]   Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus [J].
Damiola, F ;
Le Minh, N ;
Preitner, N ;
Kornmann, B ;
Fleury-Olela, F ;
Schibler, U .
GENES & DEVELOPMENT, 2000, 14 (23) :2950-2961
[3]   DIURNAL RHYTHM OF PHOSPHORYLATION OF RAT-LIVER ACETYL COA CARBOXYLASE BY THE AMP-ACTIVATED PROTEIN-KINASE, DEMONSTRATED USING FREEZE-CLAMPING - EFFECTS OF HIGH-FAT DIETS [J].
DAVIES, SP ;
CARLING, D ;
MUNDAY, MR ;
HARDIE, DG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 203 (03) :615-623
[4]   Short-term overexpression of a constitutively active form of AMP-activated protein kinase in the liver leads to mild hypoglycemia and fatty liver [J].
Foretz, M ;
Ancellin, N ;
Amdreelli, F ;
Saintillan, Y ;
Grondin, P ;
Kahn, A ;
Thorens, B ;
Vaulont, S ;
Viollet, B .
DIABETES, 2005, 54 (05) :1331-1339
[5]   Proteasomes keep the circadian clock ticking [J].
Gatfield, David ;
Schibler, Ueli .
SCIENCE, 2007, 316 (5828) :1135-1136
[6]   The meter of metabolism [J].
Green, Carla B. ;
Takahashi, Joseph S. ;
Bass, Joseph .
CELL, 2008, 134 (05) :728-742
[7]   AMPK phosphorylation of raptor mediates a metabolic checkpoint [J].
Gwinn, Dana M. ;
Shackelford, David B. ;
Egan, Daniel F. ;
Mihaylova, Maria M. ;
Mery, Annabelle ;
Vasquez, Debbie S. ;
Turk, Benjamin E. ;
Shaw, Reuben J. .
MOLECULAR CELL, 2008, 30 (02) :214-226
[8]   AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy [J].
Hardie, D. Grahame .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (10) :774-785
[9]   The AMP-activated protein kinase pathway - new players upstream and downstream [J].
Hardie, DG .
JOURNAL OF CELL SCIENCE, 2004, 117 (23) :5479-5487
[10]   Glucose down-regulates Per1 and Per2 mRNA levels and induces circadian gene expression in cultured rat-1 fibroblasts [J].
Hirota, T ;
Okano, T ;
Kokame, K ;
Shirotani-Ikejima, H ;
Miyata, T ;
Fukada, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :44244-44251