Transcriptional regulation of human DNA repair genes following genotoxic stress: trigger mechanisms, inducible responses and genotoxic adaptation

被引:185
作者
Christmann, Markus [1 ]
Kaina, Bernd [1 ]
机构
[1] Univ Med Ctr, Dept Toxicol, D-55131 Mainz, Germany
关键词
BASE EXCISION-REPAIR; NF-KAPPA-B; MESSENGER-RNA EXPRESSION; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE MGMT; DEPENDENT NUCLEAR-DYNAMICS; INDUCED ADAPTIVE RESPONSE; MAMMARY EPITHELIAL-CELLS; TUMOR-SUPPRESSOR P53; DOUBLE-STRAND BREAKS; HAMSTER OVARY CELLS;
D O I
10.1093/nar/gkt635
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
DNA repair is the first barrier in the defense against genotoxic stress. In recent years, mechanisms that recognize DNA damage and activate DNA repair functions through transcriptional upregulation and post-translational modification were the focus of intensive research. Most DNA repair pathways are complex, involving many proteins working in discrete consecutive steps. Therefore, their balanced expression is important for avoiding erroneous repair that might result from excessive base removal and DNA cleavage. Amelioration of DNA repair requires both a fine-tuned system of lesion recognition and transcription factors that regulate repair genes in a balanced way. Transcriptional upregulation of DNA repair genes by genotoxic stress is counteracted by DNA damage that blocks transcription. Therefore, induction of DNA repair resulting in an adaptive response is only visible through a narrow window of dose. Here, we review transcriptional regulation of DNA repair genes in normal and cancer cells and describe mechanisms of promoter activation following genotoxic exposures through environmental carcinogens and anticancer drugs. The data available to date indicate that 25 DNA repair genes are subject to regulation following genotoxic stress in rodent and human cells, but for only a few of them, the data are solid as to the mechanism, homeostatic regulation and involvement in an adaptive response to genotoxic stress.
引用
收藏
页码:8403 / 8420
页数:18
相关论文
共 200 条
  • [1] p53 and DNA damage-inducible expression of the xeroderma pigmentosum group C gene
    Adimoolam, S
    Ford, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) : 12985 - 12990
  • [2] A nucleotide excision repair master-switch: p53 regulated coordinate induction of global genomic repair genes
    Amundson, SA
    Patterson, A
    Do, KT
    Fornace, AJ
    [J]. CANCER BIOLOGY & THERAPY, 2002, 1 (02) : 145 - 149
  • [3] BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase a
    Anderson, SE
    Schlegel, BP
    Nakajima, T
    Wolpin, ES
    Parvin, JD
    [J]. NATURE GENETICS, 1998, 19 (03) : 254 - 256
  • [4] P53 modulates homologous recombination by transcriptional regulation of the RAD51 gene
    Arias-Lopez, C
    Lazaro-Trueba, I
    Kerr, P
    Lord, CJ
    Dexter, T
    Iravani, M
    Ashworth, A
    Silva, A
    [J]. EMBO REPORTS, 2006, 7 (02) : 219 - 224
  • [5] RADIATION-INDUCED ADAPTIVE RESPONSE FOR PROTECTION AGAINST MICRONUCLEUS FORMATION AND NEOPLASTIC TRANSFORMATION IN C3H 10T1/2 MOUSE EMBRYO CELLS
    AZZAM, EI
    RAAPHORST, GP
    MITCHEL, REJ
    [J]. RADIATION RESEARCH, 1994, 138 (01) : S28 - S31
  • [6] DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
    Bakkenist, CJ
    Kastan, MB
    [J]. NATURE, 2003, 421 (6922) : 499 - 506
  • [7] Enhanced phosphorylation of p53 by ATN in response to DNA damage
    Banin, S
    Moyal, L
    Shieh, SY
    Taya, Y
    Anderson, CW
    Chessa, L
    Smorodinsky, NI
    Prives, C
    Reiss, Y
    Shiloh, Y
    Ziv, Y
    [J]. SCIENCE, 1998, 281 (5383) : 1674 - 1677
  • [8] Malignant melanoma cells acquire resistance to DNA interstrand cross-linking chemotherapeutics by p53-triggered upregulation of DDB2/XPC-mediated DNA repair
    Barckhausen, C.
    Roos, W. P.
    Naumann, S. C.
    Kaina, B.
    [J]. ONCOGENE, 2014, 33 (15) : 1964 - 1974
  • [9] Differential sensitivity of malignant glioma cells to methylating and chloroethylating anticancer drugs:: p53 determines the switch by regulating xpc, ddb2, and DNA double-strand breaks
    Batista, Luis F. Z.
    Roos, Wynand P.
    Christmann, Markus
    Menck, Carlos F. M.
    Kaina, Bernd
    [J]. CANCER RESEARCH, 2007, 67 (24) : 11886 - 11895
  • [10] Human monocytes are severely impaired in base and DNA double-strand break repair that renders them vulnerable to oxidative stress
    Bauer, Martina
    Goldstein, Michael
    Christmann, Markus
    Becker, Huong
    Heylmann, Daniel
    Kaina, Bernd
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (52) : 21105 - 21110