DNA-damage repair; the good, the bad, and the ugly

被引:336
作者
Hakem, Razqallah [1 ,2 ]
机构
[1] Univ Toronto, Dept Med Biophys, Ontario Canc Inst, UHN, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Immunol, Ontario Canc Inst, UHN, Toronto, ON M5G 2M9, Canada
关键词
cancer; DNA repair; mouse models; syndromes;
D O I
10.1038/emboj.2008.15
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
Organisms have developed several DNA-repair pathways as well as DNA-damage checkpoints to cope with the frequent challenge of endogenous and exogenous DNA insults. In the absence or impairment of such repair or checkpoint mechanisms, the genomic integrity of the organism is often compromised. This review will focus on the functional consequences of impaired DNA-repair pathways. Although each pathway is addressed individually, it is essential to note that cross talk exists between repair pathways, and that there are instances in which a DNA-repair protein is involved in more than one pathway. It is also important to integrate DNA-repair process with DNA-damage checkpoints and cell survival, to gain a better understanding of the consequences of compromised DNA repair at both cellular and organismic levels. Functional consequences associated with impaired DNA repair include embryonic lethality, shortened life span, rapid ageing, impaired growth, and a variety of syndromes, including a pronounced manifestation of cancer.
引用
收藏
页码:589 / 605
页数:17
相关论文
共 188 条
[1]   Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA [J].
Aas, PA ;
Otterlei, M ;
Falnes, PO ;
Vågbo, CB ;
Skorpen, F ;
Akbari, M ;
Sundheim, O ;
Bjorås, M ;
Slupphaug, G ;
Seeberg, E ;
Krokan, HE .
NATURE, 2003, 421 (6925) :859-863
[2]   Eme1 is involved in DNA damage processing and maintenance of genomic stability in mammalian cells [J].
Abraham, J ;
Lemmers, B ;
Hande, MP ;
Moynahan, ME ;
Chahwan, C ;
Ciccia, A ;
Essers, J ;
Hanada, K ;
Chahwan, R ;
Khaw, AK ;
McPherson, P ;
Shehabeldin, A ;
Laister, R ;
Arrowsmith, C ;
Kanaar, R ;
West, SC ;
Jasin, M ;
Hakem, R .
EMBO JOURNAL, 2003, 22 (22) :6137-6147
[3]   A role for Xrcc2 in the early stages of mouse development [J].
Adam, Julie ;
Deans, Bryan ;
Thacker, John .
DNA REPAIR, 2007, 6 (02) :224-234
[4]   XLF interacts with the XRCC4-DNA ligase IV complex to promote DNA nonhomologous end-joining [J].
Ahnesorg, P ;
Smith, P ;
Jackson, SP .
CELL, 2006, 124 (02) :301-313
[5]   An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria [J].
Andressoo, Jaan-Olle ;
Mitchell, James R. ;
de Wit, Jan ;
Hoogstraten, Deborah ;
Volker, Marcel ;
Toussaint, Wendy ;
Speksnijder, Ewoud ;
Beems, Rudolph B. ;
van Steeg, Harry ;
Jans, Judith ;
de Zeeuw, Chris I. ;
Jaspers, Nicolaas G. J. ;
Raams, Anja ;
Lehmann, Alan R. ;
Vermeulen, Wim ;
Hoeijmakers, Jan H. J. ;
van der Horst, Gijsbertus T. J. .
CANCER CELL, 2006, 10 (02) :121-132
[6]   Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over [J].
Baker, SM ;
Plug, AW ;
Prolla, TA ;
Bronner, CE ;
Harris, AC ;
Yao, X ;
Christie, DM ;
Monell, C ;
Arnheim, N ;
Bradley, A ;
Ashley, T ;
Liskay, RM .
NATURE GENETICS, 1996, 13 (03) :336-342
[7]   MALE-MICE DEFECTIVE IN THE DNA MISMATCH REPAIR GENE PMS2 EXHIBIT ABNORMAL CHROMOSOME SYNAPSIS IN MEIOSIS [J].
BAKER, SM ;
BRONNER, CE ;
ZHANG, L ;
PLUG, AW ;
ROBATZEK, M ;
WARREN, G ;
ELLIOTT, EA ;
YU, JA ;
ASHLEY, T ;
ARNHEIM, N ;
FLAVELL, RA ;
LISKAY, RM .
CELL, 1995, 82 (02) :309-319
[8]   Altered somatic hypermutation and reduced class-switch recombination in exonuclease 1-mutant mice [J].
Bardwell, PD ;
Woo, CJ ;
Wei, KC ;
Li, ZQ ;
Martin, A ;
Sack, SZ ;
Parris, T ;
Edelmann, W ;
Scharff, MD .
NATURE IMMUNOLOGY, 2004, 5 (02) :224-229
[9]   Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice [J].
Barnes, DE ;
Stamp, G ;
Rosewell, I ;
Denzel, A ;
Lindahl, T .
CURRENT BIOLOGY, 1998, 8 (25) :1395-1398
[10]  
Becker K, 1997, CANCER RES, V57, P3335