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
  • [151] Tumor suppressor p53 represses transcription of RECQ4 helicase
    Sengupta, S
    Shimamoto, A
    Koshiji, M
    Pedeux, R
    Rusin, M
    Spillare, EA
    Shen, JC
    Huang, LE
    Lindor, NM
    Furuichi, Y
    Harris, CC
    [J]. ONCOGENE, 2005, 24 (10) : 1738 - 1748
  • [152] ADAPTIVE RESPONSE TO IONIZING-RADIATION INDUCED BY LOW-DOSES OF GAMMA-RAYS IN HUMAN CELL-LINES
    SEONG, J
    SUH, CO
    KIM, GE
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 33 (04): : 869 - 874
  • [153] Characterization of Trex1 Induction by IFN-γ in Murine Macrophages
    Serra, Maria
    Forcales, Sonia-Vanina
    Pereira-Lopes, Selma
    Lloberas, Jorge
    Celada, Antonio
    [J]. JOURNAL OF IMMUNOLOGY, 2011, 186 (04) : 2299 - 2308
  • [154] SHAFMAN TD, 1995, CANCER RES, V55, P3242
  • [155] Binding sequence-dopendent regulation of the human proliferating cell nuclear antigen promoter by p53
    Shan, B
    Morris, GF
    [J]. EXPERIMENTAL CELL RESEARCH, 2005, 305 (01) : 10 - 22
  • [156] Induction of p53-dependent activation of the human proliferating cell nuclear antigen gene in chromatin by ionizing radiation
    Shan, B
    Xu, J
    Zhuo, Y
    Morris, CA
    Morris, GF
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (45) : 44009 - 44017
  • [157] Shieh SY, 2000, GENE DEV, V14, P289
  • [158] SHIVAKUMAR CV, 1995, MOL CELL BIOL, V15, P6785
  • [159] Srivenugopal KS, 2001, CLIN CANCER RES, V7, P1398
  • [160] The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair
    Starita, LM
    Parvin, JD
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (03) : 345 - 350