DNA polymerases are error-prone at RecA-mediated recombination intermediates

被引:17
|
作者
Pomerantz, Richard T. [1 ]
Goodman, Myron F. [2 ]
O'Donnell, Michael E. [3 ]
机构
[1] Temple Univ, Sch Med, Fels Inst Canc Res, Dept Biochem, Philadelphia, PA 19122 USA
[2] Univ So Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
[3] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
DNA replication; homologous recombination; double-strand break repair; stress-induced mutagenesis; adaptive mutagenesis; break-induced replication; STRESS-INDUCED MUTAGENESIS; BREAK-INDUCED REPLICATION; ESCHERICHIA-COLI; KINETIC MECHANISM; ADAPTIVE MUTATION; HIGH-FIDELITY; REPAIR; BACTERIA; DINB; SWITCH;
D O I
10.4161/cc.25691
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genetic studies have suggested that Y-family translesion DNA polymerase IV (DinB) performs error-prone recombination-directed replication (RDR) under conditions of stress due to its ability to promote mutations during double-strand break (DSB) repair in growth-limited E. coli cells. In recent studies we have demonstrated that pol IV is preferentially recruited to D-loop recombination intermediates at stress-induced concentrations and is highly mutagenic during RDR in vitro. These findings verify longstanding genetic data that have implicated pol IV in promoting stress-induced mutagenesis at D-loops. In this Extra View, we demonstrate the surprising finding that A-family pol I, which normally exhibits high-fidelity DNA synthesis, is highly error-prone at D-loops like pol IV. These findings indicate that DNA polymerases are intrinsically error-prone at RecA-mediated D-loops and suggest that auxiliary factors are necessary for suppressing mutations during RDR in non-stressed proliferating cells.
引用
收藏
页码:2558 / 2563
页数:6
相关论文
共 50 条
  • [41] Modulation of RecFORQ- and RecA-Mediated Homologous Recombination in Escherichia coli by Isoforms of Translation Initiation Factor IF2
    Mallikarjun, Jillella
    SaiSree, L.
    Himabindu, P.
    Anupama, K.
    Reddy, Manjula
    Gowrishankar, J.
    JOURNAL OF BACTERIOLOGY, 2022, 204 (04)
  • [42] Escherichia coli Rep DNA helicase and error-prone DNA polymerase IV interact physically and functionally
    Sladewski, Thomas E.
    Hetrick, Kyle M.
    Foster, Patricia L.
    MOLECULAR MICROBIOLOGY, 2011, 80 (02) : 524 - 541
  • [43] The extent of error-prone replication restart by homologous recombination is controlled by Exo1 and checkpoint proteins
    Tsang, Ellen
    Miyabe, Izumi
    Iraqui, Ismail
    Zheng, Jiping
    Lambert, Sarah A. E.
    Carr, Antony M.
    JOURNAL OF CELL SCIENCE, 2014, 127 (13) : 2983 - 2994
  • [44] A Unique B-Family DNA Polymerase Facilitating Error-Prone DNA Damage Tolerance in Crenarchaeota
    Feng, Xu
    Liu, Xiaotong
    Xu, Ruyi
    Zhao, Ruiliang
    Feng, Wenqian
    Liao, Jianglan
    Han, Wenyuan
    She, Qunxin
    FRONTIERS IN MICROBIOLOGY, 2020, 11
  • [45] Residues in the fingers domain of the translesion DNA polymerase DinB enable its unique participation in error-prone double-strand break repair
    Tashjian, Tommy F.
    Danilowicz, Claudia
    Molza, Anne-Elizabeth
    Nguyen, Brian H.
    Prevost, Chantal
    Prentiss, Mara
    Godoy, Veronica G.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2019, 294 (19) : 7588 - 7600
  • [46] RNA facilitates RecA-mediated DNA pairing and strand transfer between molecules bearing limited regions of homology
    Kotani, H
    Germann, MW
    Andrus, A
    Vinayak, R
    Mullah, B
    Kmiec, EB
    MOLECULAR & GENERAL GENETICS, 1996, 250 (05): : 626 - 634
  • [47] Error-prone DNA repair pathways as determinants of immunotherapy activity: an emerging scenario for cancer treatment
    Caracciolo, Daniele
    Riillo, Caterina
    Arbitrio, Mariamena
    Di Martino, Maria Teresa
    Tagliaferri, Pierosandro
    Tassone, Pierfrancesco
    INTERNATIONAL JOURNAL OF CANCER, 2020, 147 (10) : 2658 - 2668
  • [48] Directed Evolution of an Error-Prone T7 DNA Polymerase that Attenuates Viral Replication
    Soete, Sandra
    Kleine, Stefan
    Schlicke, Marina
    Brakmann, Susanne
    CHEMBIOCHEM, 2011, 12 (10) : 1551 - 1558
  • [49] Genotoxic therapy stimulates error-prone DNA repair in dormant hepatocellular cancer stem cells
    Nishikawa, Shimpei
    Ishii, Hideshi
    Haraguchi, Naotsugu
    Kano, Yoshihiro
    Fukusumi, Takahito
    Ohta, Katsuya
    Ozaki, Miyuki
    Sakai, Daisuke
    Satoh, Taroh
    Nagano, Hiroaki
    Doki, Yuichiro
    Mori, Masaki
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2012, 3 (06) : 959 - 962
  • [50] Enhancement of RecA-mediated self-assembly in DNA nanostructures through basepair mismatches and single-strand nicks
    Corbett, Sybilla Louise
    Sharma, Rajan
    Davies, Alexander Giles
    Walti, Christoph
    SCIENTIFIC REPORTS, 2017, 7