4.3 Article

ARTD1 (PARP1) activation and NAD(+) in DNA repair and cell death

Journal

DNA REPAIR
Volume 23, Issue -, Pages 27-32

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.dnarep.2014.09.004

Keywords

NAD(+); ADP(ribosyl)ation; Energy depletion; Metabolic defects

Funding

  1. National Institute of Health (NIH) [CA148629, ES022291]
  2. NATIONAL CANCER INSTITUTE [R01CA148629] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R21ES022291] Funding Source: NIH RePORTER

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Nicotinamide adenine dinucleotide, NAD(+), is a small metabolite coenzyme that is essential for the progress of crucial cellular pathways including glycolysis, the tricarboxylic acid cycle (TCA) and mitochondrial respiration. These processes consume and produce both oxidative and reduced forms of NAD (NAD(+) and NADH). NAD(+) is also important for ADP(ribosyl)ation reactions mediated by the ADP-ribosyltransferase enzymes (ARTDs) or deacetylation reactions catalyzed by the sirtuins (SIRTs) which use NAD(+) as a substrate. In this review, we highlight the significance of NAD(+) catabolism in DNA repair and cell death through its utilization by ARTDs and SIRTs. We summarize the current findings on the involvement of ARTD1 activity in DNA repair and most specifically its involvement in the trigger of cell death mediated by ARTD1 activation and energy depletion. By sharing the same substrate, the activities of ARTDs and SIRTs are tightly linked, are dependent on each other and are thereby involved in the same cellular processes that play an important role in cancer biology, inflammatory diseases and ischaemia/reperfusion. (C) 2014 Elsevier B.V. All rights reserved.

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