PARP1 Val762Ala polymorphism reduces enzymatic activity

Poly(ADP-ribose) polymerase 1 (PARP1) modifies a variety of nuclear proteins by poly(ADP-ribosyl)ation, and plays diverse roles in molecular and cellular processes. A common PARP1 single nucleotide polymorphism (SNP) at codon 762, resulting in the substitution of alanine (Ala) for valine (Va1) in the catalytic domain has been implicated in susceptibility to cancer. To characterize the functional effect of this polymorphism on PARP1, we performed in vitro enzymatic analysis on PARP1-Ala762 and PARP1-Val762. We found that PARP1-Ala762 displayed 57.2% of the activity of PARP1-Va1762 for auto-poly(ADP-ribosyl)ation and 61.9% of the activity of PARP1-Va1762 for traps-poly(ADP-ribosyl)ation of historic H1. The kinetic characterization revealed that the K-m of PARP1-Ala762 was increased to a 1.2-fold of the K-m of PARP1-Va1762 for traps-poly(ADP-ribosyl)ation. Thus, the PARP1 Va1762A1a polymorphism reduces the enzymatic activity of PARP1 by increasing K-m. This finding suggests that different levels of poly(ADP-ribosyl)ation by PARP1 might aid in understanding the cancer risk of carriers of the PARP1 Va1762A1a polymorphism. (c) 2006 Elsevier Inc. All rights reserved.