Regulation of clock and NPAS2 DNA binding by the redox state of NAD cofactors

J Rutter, M Reick, LC Wu, SL McKnight - Science, 2001 - science.org
J Rutter, M Reick, LC Wu, SL McKnight
Science, 2001science.org
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 …
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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