Repairing DNA double-strand breaks by the prokaryotic non-homologous end-joining pathway

被引:26
作者
Brissett, Nigel C. [1 ]
Doherty, Aidan J. [1 ]
机构
[1] Univ Sussex, Genome Damage & Stabil Ctr, Brighton BN1 9RQ, E Sussex, England
基金
英国生物技术与生命科学研究理事会;
关键词
bacterium; DNA ligase; DNA repair; Ku; non-homologous end-joining (NHEJ); polymerase; LIGASE-D; BACILLUS-SUBTILIS; BACTERIAL-DNA; SUBSTRATE-SPECIFICITY; IONIZING-RADIATION; POLYMERASE-MU; KU; PROTEINS; PRIMASE; DOMAIN;
D O I
10.1042/BST0370539
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The NHEJ (non-homologous end-joining) pathway is one of the major mechanisms for repairing DSBs (double-strand breaks) that occur in genomic DNA. In common with eukaryotic organisms, many prokaryotes possess a conserved NHEJ apparatus that is essential for the repair of DSBs arising in the stationary phase of the cell cycle. Although the bacterial NHEJ complex is much more minimal than its eukaryotic counterpart, both pathways share a number of common mechanistic features. The relative simplicity of the prokaryotic NHEJ complex makes it a tractable model system for investigating the cellular and molecular mechanisms of DSB repair. The present review describes recent advances in our understanding of prokaryotic end-joining, focusing primarily on biochemical, structural and cellular aspects of the mycobacterial NHEJ repair pathway.
引用
收藏
页码:539 / 545
页数:7
相关论文
共 50 条
  • [21] Repair of DNA Double-Strand Breaks by the Nonhomologous End Joining Pathway
    Stinson, Benjamin M.
    Loparo, Joseph J.
    ANNUAL REVIEW OF BIOCHEMISTRY, VOL 90, 2021, 2021, 90 : 137 - 164
  • [22] Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells
    Takata, M
    Sasaki, MS
    Sonoda, E
    Morrison, C
    Hashimoto, M
    Utsumi, H
    Yamaguchi-Iwai, Y
    Shinohara, A
    Takeda, S
    EMBO JOURNAL, 1998, 17 (18) : 5497 - 5508
  • [23] The Saccharomyces cerevisiae DNA damage checkpoint is required for efficient repair of double strand breaks by non-homologous end joining
    de la Torre-Ruiz, MA
    Lowndes, NF
    FEBS LETTERS, 2000, 467 (2-3) : 311 - 315
  • [24] Ku Regulates the Non-Homologous End Joining Pathway Choice of DNA Double-Strand Break Repair in Human Somatic Cells
    Fattah, Farjana
    Lee, Eu Han
    Weisensel, Natalie
    Wang, Yongbao
    Lichter, Natalie
    Hendrickson, Eric A.
    PLOS GENETICS, 2010, 6 (02):
  • [25] The alternative end-joining pathway for repair of DNA double-strand breaks requires PARP1 but is not dependent upon microhomologies
    Mansour, Wael Y.
    Rhein, Tim
    Dahm-Daphi, Jochen
    NUCLEIC ACIDS RESEARCH, 2010, 38 (18) : 6065 - 6077
  • [26] Competing roles of DNA end resection and non-homologous end joining functions in the repair of replication-born double-strand breaks by sister-chromatid recombination
    Munoz-Galvan, Sandra
    Lopez-Saavedra, Ana
    Jackson, Stephen P.
    Huertas, Pablo
    Cortes-Ledesma, Felipe
    Aguilera, Andres
    NUCLEIC ACIDS RESEARCH, 2013, 41 (03) : 1669 - 1683
  • [27] IGF-1R inhibition enhances radiosensitivity and delays double-strand break repair by both non-homologous end-joining and homologous recombination
    Chitnis, M. M.
    Lodhia, K. A.
    Aleksic, T.
    Gao, S.
    Protheroe, A. S.
    Macaulay, V. M.
    ONCOGENE, 2014, 33 (45) : 5262 - 5273
  • [28] DNA non-homologous end-joining enters the resection arena
    Jeggo, Penny A.
    Loebrich, Markus
    ONCOTARGET, 2017, 8 (55) : 93317 - 93318
  • [29] The role of the nonhomologous end-joining DNA double-strand break repair pathway in telomere biology
    Riha, Karel
    Heacock, Michelle L.
    Shippen, Dorothy E.
    ANNUAL REVIEW OF GENETICS, 2006, 40 : 237 - 277
  • [30] Influence of reduced glutathione on end-joining of DNA double-strand breaks: Cytogenetical and molecular approach
    Ghoshal, Nitin
    Sharma, Sheetal
    Banerjee, Atanu
    Kurkalang, Sillarine
    Raghavan, Sathees C.
    Chatterjee, Anupam
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2017, 795 : 1 - 9