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Identification of a DNA nonhomologous end-joining complex in bacteria
被引:252
|作者:
Weller, GR
Kysela, B
Roy, R
Tonkin, LM
Scanlan, E
Della, M
Devine, SK
Day, JP
Wilkinson, A
di Fagagna, FD
Devine, KM
Bowater, RP
Jeggo, PA
Jackson, SP
Doherty, AJ
机构:
[1] Univ Cambridge, Cambridge Inst Med Res, Cambridge CB2 2XY, England
[2] Univ Cambridge, Dept Haematol, Cambridge CB2 2XY, England
[3] Univ Sussex, Genome Damage & Stabil Ctr, Brighton BN1 9RQ, E Sussex, England
[4] Univ Cambridge, Dept Zool, Cambridge CB2 1QR, England
[5] Univ Cambridge, Wellcome Trust Canc Res UK, Inst Canc & Dev Biol, Cambridge CB2 1QR, England
[6] Univ Dublin Trinity Coll, Smurfit Inst, Dept Genet, Dublin 2, Ireland
[7] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
来源:
关键词:
D O I:
10.1126/science.1074584
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
in eukaryotic cells, double-strand breaks (DSBs) in DNA are generally repaired by the pathway of homologous recombination or by DNA nonhomologous end joining (NHEJ). Both pathways have been highly conserved throughout eukaryotic evolution, but no equivalent NHEJ system has been identified in prokaryotes. The NHEJ pathway requires a DNA end-binding component called Ku. We have identified bacterial Ku homologs and show that these proteins retain the biochemical characteristics of the eukaryotic Ku heterodimer. Furthermore, we show that bacterial Ku specifically recruits DNA ligase to DNA ends and stimulates DNA ligation. Loss of these proteins leads to hypersensitivity to ionizing radiation in Bacillus subtilis. These data provide evidence that many bacteria possess a DNA DSB repair apparatus that shares many features with the NHEJ system of eukarya and suggest that this DNA repair pathway arose before the prokaryotic and eukaryotic lineages diverged.
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页码:1686 / 1689
页数:4
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