Rapid repair of DNA double strand breaks in Arabidopsis thaliana is dependent on proteins involved in chromosome structure maintenance

被引:56
|
作者
Kozak, Jaroslav [1 ]
West, Christopher E. [2 ]
White, Charles [3 ]
da Costa-Nunes, Jose A. [4 ]
Angelis, Karel J. [1 ]
机构
[1] Inst Expt Bot AS CR, Prague 16000 6, Czech Republic
[2] Univ Leeds, CPS, Fac Biol Sci, Leeds LS2 9JT, W Yorkshire, England
[3] Clermont Univ, CNRS, UMR 6247, INSERM,U931, F-63177 Aubiere, France
[4] Univ Tecn Lisboa, ISA, P-1349017 Lisbon, Portugal
基金
英国生物技术与生命科学研究理事会;
关键词
AtKU80; AtRAD21.1; AtLIG4-4; MIM; Bleomycin; Comet assay; CELL GEL-ELECTROPHORESIS; COMET ASSAY; SINGLE-STRAND; HOMOLOGOUS RECOMBINATION; IONIZING-RADIATION; SMC PROTEINS; LIGASE-IV; DAMAGE; BLEOMYCIN; PLANTS;
D O I
10.1016/j.dnarep.2008.11.012
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA double strand breaks (DSBs) are one of the most cytotoxic forms of DNA damage and must be repaired by recombination, predominantly via non-homologous joining of DNA ends (NHEJ) in higher eukaryotes. However, analysis of DSB repair kinetics of plant NHEJ mutants atlig4-4 and atku80 with the neutral comet assay shows that alternative DSB repair pathways are active. Surprisingly, these kinetic measurements show that DSB repair was faster in the NHEJ mutant lines than in wild-type Arabidopsis. Here we provide the first characterization of this KU-independent, rapid DSB repair pathway operating in Arabidopsis. The alternate pathway that rapidly removes the majority of DSBs present in nuclear DNA depends upon structural maintenance of chromosomes (SMC) complex proteins, namely MIM/AtRAD18 and AtRAD21.1. An absolute requirement for SMC proteins and kleisin for rapid repair of DSBs in Arabidopsis opens new insight into the mechanism of DSB removal in plants. Crown Copyright (C) 2008 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:413 / 419
页数:7
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