Crosstalk between poly(ADP-ribose) polymerase and sirtuin enzymes

被引:197
作者
Canto, Caries [1 ]
Sauve, Anthony A. [2 ]
Bai, Peter [3 ,4 ]
机构
[1] Nestle Inst Hlth Sci, CH-1015 Lausanne, Switzerland
[2] Weill Cornell Med Coll, Dept Pharmacol, New York, NY 10021 USA
[3] Univ Debrecen, Dept Med Chem, Med & Hlth Sci Ctr, H-4032 Debrecen, Hungary
[4] MTA DE Cell Biol & Signaling Res Grp, H-4032 Debrecen, Hungary
关键词
Poly(ADP-ribose) polymerase; Sirtuins SIRT1; NAD(+); Metabolism; Oxidative stress; Mitochondria; NICOTINAMIDE-ADENINE-DINUCLEOTIDE; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; ADENOSINE-DIPHOSPHATE RIBOSYLATION; REGULATES INSULIN-SECRETION; PREVENTS NAD(+) DEPLETION; SMALL-MOLECULE ACTIVATORS; COLONY-ENHANCING FACTOR; PROMOTES CELL-SURVIVAL; BASE EXCISION-REPAIR;
D O I
10.1016/j.mam.2013.01.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly(ADP-ribose) polymerases (PARPs) are NAD(+) dependent enzymes that were identified as DNA repair proteins, however, today it seems clear that PARPs are responsible for a plethora of biological functions. Sirtuins (SIRTs) are HAW-dependent deacetylase enzymes involved in the same biological processes as PARPs raising the question whether PARP and SIRT enzymes may interact with each other in physiological and pathophysiological conditions. Hereby we review the current understanding of the SIRT-PARP interplay in regard to the biochemical nature of the interaction (competition for the common NAD(+) substrate, mutual posttranslational modifications and direct transcriptional effects) and the physiological or pathophysiological consequences of the interactions (metabolic events, oxidative stress response, genomic stability and aging). Finally, we give an overview of the possibilities of pharmacological intervention to modulate PARP and SIRT enzymes either directly, or through modulating NAD(+) homeostasis. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1168 / 1201
页数:34
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