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Biosensor reveals multiple sources for mitochondrial NAD?.


ABSTRACT: Nicotinamide adenine dinucleotide (NAD(+)) is an essential substrate for sirtuins and poly(adenosine diphosphate-ribose) polymerases (PARPs), which are NAD(+)-consuming enzymes localized in the nucleus, cytosol, and mitochondria. Fluctuations in NAD(+) concentrations within these subcellular compartments are thought to regulate the activity of NAD(+)-consuming enzymes; however, the challenge in measuring compartmentalized NAD(+) in cells has precluded direct evidence for this type of regulation. We describe the development of a genetically encoded fluorescent biosensor for directly monitoring free NAD(+) concentrations in subcellular compartments. We found that the concentrations of free NAD(+) in the nucleus, cytoplasm, and mitochondria approximate the Michaelis constants for sirtuins and PARPs in their respective compartments. Systematic depletion of enzymes that catalyze the final step of NAD(+) biosynthesis revealed cell-specific mechanisms for maintaining mitochondrial NAD(+) concentrations.

SUBMITTER: Cambronne XA 

PROVIDER: S-EPMC6530784 | biostudies-literature | 2016 Jun

REPOSITORIES: biostudies-literature

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Biosensor reveals multiple sources for mitochondrial NAD⁺.

Cambronne Xiaolu A XA   Stewart Melissa L ML   Kim DongHo D   Jones-Brunette Amber M AM   Morgan Rory K RK   Farrens David L DL   Cohen Michael S MS   Goodman Richard H RH  

Science (New York, N.Y.) 20160601 6292


Nicotinamide adenine dinucleotide (NAD(+)) is an essential substrate for sirtuins and poly(adenosine diphosphate-ribose) polymerases (PARPs), which are NAD(+)-consuming enzymes localized in the nucleus, cytosol, and mitochondria. Fluctuations in NAD(+) concentrations within these subcellular compartments are thought to regulate the activity of NAD(+)-consuming enzymes; however, the challenge in measuring compartmentalized NAD(+) in cells has precluded direct evidence for this type of regulation.  ...[more]

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