PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks

被引:67
作者
Couto, C. Anne-Marie [1 ]
Wang, Hong-Yu [1 ]
Green, Joanna C. A. [1 ]
Kiely, Rhian [1 ]
Siddaway, Robert [1 ]
Borer, Christine [1 ]
Pears, Catherine J. [1 ]
Lakin, Nicholas D. [1 ]
机构
[1] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
基金
英国生物技术与生命科学研究理事会;
关键词
DEPENDENT PROTEIN-KINASE; DNA-DAMAGE; POLY(ADP-RIBOSE) POLYMERASE-1; CELLULAR-RESPONSES; APLF C2ORF13; REPAIR; DICTYOSTELIUM; INVOLVEMENT; SUPPRESSION; COMPLEX;
D O I
10.1083/jcb.201012132
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Poly adenosine diphosphate (ADP)-ribosylation (PARylation) by poly ADP-ribose (PAR) polymerases (PARPs) is an early response to DNA double-strand breaks (DSBs). In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PARylation in regulating nonhomologous end joining (NHEJ). PARylation occurred at single-strand breaks, and two PARPs, Adprt1b and Adprt2, were required for resistance to this kind of DNA damage. In contrast, although Adprt1b was dispensable for PARylation at DSBs, Adprt1a and, to a lesser extent, Adprt2 were required for this event. Disruption of adprt2 had a subtle impact on the ability of cells to perform NHEJ. However, disruption of adprt1a decreased the ability of cells to perform end joining with a concomitant increase in homologous recombination. PAR-dependent regulation of NHEJ was achieved through promoting recruitment and/or retention of Ku at DSBs. Furthermore, a PAR interaction motif in Ku70 was required for this regulation and efficient NHEJ. These data illustrate that PARylation at DSBs promotes NHEJ through recruitment or retention of repair factors at sites of DNA damage.
引用
收藏
页码:367 / 375
页数:9
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