Metabolism control by the circadian clock and vice versa

被引:119
作者
Eckel-Mahan, Kristin [1 ]
Sassone-Corsi, Paolo [1 ]
机构
[1] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92717 USA
基金
美国国家卫生研究院;
关键词
REV-ERB-ALPHA; CELL-DEATH; POLY(ADP-RIBOSE) POLYMERASE-1; ESSENTIAL COMPONENTS; GLUCOSE-HOMEOSTASIS; NAD BIOSYNTHESIS; OXIDATIVE STRESS; SIRT1; ACTIVATION; MOUSE; EXPRESSION;
D O I
10.1038/nsmb.1595
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circadian rhythms govern a wide variety of physiological and metabolic functions in most organisms. At the heart of these regulatory pathways in mammals is the clock machinery, a remarkably coordinated transcription-translation system that relies on dynamic changes in chromatin states. Recent findings indicate that regulation also goes the other way, as specific elements of the clock can sense changes in cellular metabolism. Understanding in full detail the intimate links between cellular metabolism and the circadian clock machinery will provide not only crucial insights into system physiology but also new avenues toward pharmacological intervention of metabolic disorders.
引用
收藏
页码:462 / 467
页数:6
相关论文
共 89 条
[1]   Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus [J].
Akhtar, RA ;
Reddy, AB ;
Maywood, ES ;
Clayton, JD ;
King, VM ;
Smith, AG ;
Gant, TW ;
Hastings, MH ;
Kyriacou, CP .
CURRENT BIOLOGY, 2002, 12 (07) :540-550
[2]   Nuclear receptor corepressor and histone deacetylase 3 govern circadian metabolic physiology [J].
Alenghat, Theresa ;
Meyers, Katherine ;
Mullican, Shannon E. ;
Leitner, Kirstin ;
Adeniji-Adele, Adetoun ;
Avila, Jacqueline ;
Bucan, Maja ;
Ahima, Rexford S. ;
Kaestner, Klaus H. ;
Lazar, Mitchell A. .
NATURE, 2008, 456 (7224) :997-U88
[3]   Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Cohen, H ;
Lin, SS ;
Manchester, JK ;
Gordon, JI ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18881-18890
[4]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[5]   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
[6]   Circadian rhythms in firing rate of individual suprachiasmatic nucleus neurons from adult and middle-aged mice [J].
Aujard, F ;
Herzog, ED ;
Block, GD .
NEUROSCIENCE, 2001, 106 (02) :255-261
[7]   When clocks go bad: Neurobehavioural consequences of disrupted circadian timing [J].
Barnard, Alun R. ;
Nolan, Patrick M. .
PLOS GENETICS, 2008, 4 (05)
[8]   SIRT1 is a circadian deacetylase for core clock components [J].
Belden, William J. ;
Dunlap, Jay C. .
CELL, 2008, 134 (02) :212-214
[9]   Circadian rhythms from multiple oscillators: Lessons from diverse organisms [J].
Bell-Pedersen, D ;
Cassone, VM ;
Earnest, DJ ;
Golden, SS ;
Hardin, PE ;
Thomas, TL ;
Zoran, MJ .
NATURE REVIEWS GENETICS, 2005, 6 (07) :544-556
[10]   Light pulse-induced heme and iron-associated transcripts in mouse brain: A microarray analysis [J].
Ben-Shlomo, R ;
Akhtar, RA ;
Collins, BH ;
Judah, DJ ;
Davies, R ;
Kyriacou, CP .
CHRONOBIOLOGY INTERNATIONAL, 2005, 22 (03) :455-471