| Literature DB >> 27645993 |
Guocun Huang1,2, Yunfeng Zhang2, Yongli Shan3, Shuzhang Yang4, Yogarany Chelliah4, Han Wang2, Joseph S Takahashi5,4.
Abstract
It is known that there are mechanistic links between circadian clocks and metabolic cycles. Reduced nicotinamide adenine dinucleotide (NADH) is a key metabolic cofactor in all living cells; however, it is not known whether levels of NADH oscillate or not. Here we employed REX, a bacterial NADH-binding protein, fused to the VP16 activator to convert intracellular endogenous redox balance into transcriptional readouts by a reporter gene in mammalian cells. EMSA results show that the DNA binding activity of both T- and S-REX::VP16 fusions is decreased with a reduced-to-oxidized cofactor ratio increase. Transient and stabilized cell lines bearing the REX::VP16 and the REX binding operator (ROP) exhibit two circadian luminescence cycles. Consistent with these results, NADH oscillations are observed in host cells, indicating REX can act as a NADH sensor to report intracellular dynamic redox homeostasis in mammalian cells in real time. NADH oscillations provide another metabolic signal for coupling the circadian clock and cellular metabolic states.Entities:
Keywords: Rex; biosensor; cell metabolism; circadian; nicotinamide adenine dinucleotide (NADH); oscillation; oxidation-reduction (redox)
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Year: 2016 PMID: 27645993 PMCID: PMC5104915 DOI: 10.1074/jbc.M116.728774
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157