Nicoletti Vincenzo Giuseppe, Stella Anna Maria Giuffrida
Department of Chemical Sciences, Section of Biochemistry and Molecular Biology, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.
Neurochem Res. 2003 Feb;28(2):187-94. doi: 10.1023/a:1022316914492.
A great deal of increasing evidence designs PARP as a multifunctional protein implicated in many cellular functions. Much interest is emerging to understand the precise mechanisms by which PARP mediates genome stabilization and protection against damage, as well as its involvement in cell death, either apoptotic or necrotic. Aside from the clearly established role of PARP hyperactivation in necrotic cell death, after excessive DNA damage and energy failure, it appears to be actively involved in the phenomenon of apoptosis. However, its exact role is still controversial. The identification of several enzymes sharing the poly(ADP-ribose) polymerase catalytic domain (PARPs), but with different features and subcellular localization, has opened a new perspective in the field of poly(ADP-ribosyl)ation. The picture of the role of PARP in the control of cell homeostasis became even more complex after demonstration of its implication in the regulation of gene transcription. The notion that energy failure is the sole mechanism by which PARP promotes cell death is therefore under reevaluation.
越来越多的证据表明,PARP是一种涉及多种细胞功能的多功能蛋白质。人们对了解PARP介导基因组稳定和防止损伤的精确机制,以及其在细胞凋亡或坏死性细胞死亡中的作用越来越感兴趣。除了PARP过度激活在坏死性细胞死亡中已明确确立的作用外,在DNA过度损伤和能量衰竭后,它似乎也积极参与细胞凋亡现象。然而,其确切作用仍存在争议。几种具有聚(ADP-核糖)聚合酶催化结构域(PARP)但具有不同特征和亚细胞定位的酶的鉴定,为聚(ADP-核糖基)化领域开辟了新的视角。在证明PARP参与基因转录调控后,PARP在控制细胞稳态中的作用图景变得更加复杂。因此,能量衰竭是PARP促进细胞死亡的唯一机制这一观点正在重新评估。