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Regulation of clock and NPAS2 DNA binding by the redox state of NAD cofactors
被引:747
|作者:
Rutter, J
[1
]
Reick, M
[1
]
Wu, LC
[1
]
McKnight, SL
[1
]
机构:
[1] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75390 USA
来源:
关键词:
D O I:
10.1126/science.1060698
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:
Clock:BMAL1 and NPAS2:BMAL1 are heterodimeric transcription factors that control gene expression as a function of the Light-dark cycle. Although built to fluctuate at or near a 24-hour cycle, the clock can be entrained by Light, activity, or food. Here we show that the DNA-binding activity of the Clock:BMAL1 and NPAS2:BMAL1 heterodimers is regulated by the redox state of nicotinamide adenine dinucleotide (NAD) cofactors in a purified system. The reduced forms of the redox cofactors, NAD(H) and NADP(H), strongly enhance DNA binding of the Clock:BMAL1 and NPAS2:BMAL1 heterodimers, whereas the oxidized forms inhibit. These observations raise the possibility that food, neuronal activity, or both may entrain the circadian clock by direct modulation of cellular redox state.
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页码:510 / 514
页数:5
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