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AMP-activated protein kinase as a key molecular link between metabolism and clockwork

Title
AMP-activated protein kinase as a key molecular link between metabolism and clockwork
Author(s)
Lee, YongjinKim, Eun-Kyoung
Issued Date
2013-07
Citation
Experimental and Molecular Medicine, v.45, no.7, pp.1 - 7
Type
Article
Author Keywords
AMPKcircadian clockCKICRYmetabolismSIRT1
Keywords
PERIPHERAL CLOCKPERIOD PROTEINSSKELETAL-MUSCLEEPSILON CKI-EPSILONCIRCADIAN CLOCKI-EPSILONGENE-EXPRESSIONFOOD-INTAKEDOUBLE-TIMESUPRACHIASMATIC NUCLEUS
ISSN
1226-3613
Abstract
Circadian clocks regulate behavioral, physiological and biochemical processes in a day/night cycle. Circadian oscillators have an essential role in the coordination of physiological processes with the cyclic changes in the physical environment. Such mammalian circadian clocks composed of the positive components (BMAL1 and CLOCK) and the negative components (CRY and PERIOD (PER)) are regulated by a negative transcriptional feedback loop in which PER is rate-limiting for feedback inhibition. In addition, posttranslational modification of these components is critical for setting or resetting the circadian oscillation. Circadian regulation of metabolism is mediated through reciprocal signaling between the clock and metabolic regulatory networks. AMP-activated protein kinase (AMPK) in the brain and peripheral tissue is a crucial cellular energy sensor that has a role in metabolic control. AMPK-mediated phosphorylation of CRY and Casein kinases I regulates the negative feedback control of circadian clock by proteolytic degradation. AMPK can also modulate the circadian rhythms through nicotinamide adenine dinucleotide- dependent regulation of silent information regulator 1. Growing evidence elucidates the AMPK-mediated controls of circadian clock in metabolic diseases such as obesity and diabetes. In this review, we summarize the current comprehension of AMPK-mediated regulation of the circadian rhythms. This will provide insight into understanding how their components regulate the metabolism. © 2013 KSBMB.
URI
http://hdl.handle.net/20.500.11750/3225
DOI
10.1038/emm.2013.65
Publisher
Nature Publishing Group
Related Researcher
  • 김은경 Kim, Eun-Kyoung
  • Research Interests Neural functions in metabolic diseases; 뇌신경세포와 비만; 당뇨 등의 대사 질환 관련 연구
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10.1038_emm.2013.65.pdf

10.1038_emm.2013.65.pdf

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Appears in Collections:
Department of Brain Sciences Lab of Neuro-Metabolism & Neurometabolomic Research Center 1. Journal Articles

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