Chromosomal stability and the DNA double-stranded break connection

被引:931
作者
van Gent, DC
Hoeijmakers, JHJ
Kanaar, R
机构
[1] Erasmus Univ, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[2] Univ Rotterdam Hosp Daniel, Dept Radiat Oncol, NL-3008 AE Rotterdam, Netherlands
关键词
D O I
10.1038/35056049
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome stability is of primary importance for the survival and proper functioning of all organisms. Double-stranded breaks in DNA are important threats to genome integrity because they can result in chromosomal aberrations that can affect, simultaneously, many genes, and lead to cell malfunctioning and cell death. These detrimental consequences are counteracted by two mechanistically distinct pathways of double-stranded break repair: homologous recombination and non-homologous end-joining. Recently, unexpected links between these double-stranded break-repair systems, and several human genome instability and cancer predisposition syndromes, have emerged. Now, interactions between both double-stranded break-repair pathways and other cellular processes, such as cell-cycle regulation and replication, are being unveiled.
引用
收藏
页码:196 / 206
页数:11
相关论文
共 115 条
[1]   Proteomics: new perspectives, new biomedical opportunities [J].
Banks, RE ;
Dunn, MJ ;
Hochstrasser, DF ;
Sanchez, JC ;
Blackstock, W ;
Pappin, DJ ;
Selby, PJ .
LANCET, 2000, 356 (9243) :1749-1756
[2]   Atm-deficient mice: A paradigm of ataxia telangiectasia [J].
Barlow, C ;
Hirotsune, S ;
Paylor, R ;
Liyanage, M ;
Eckhaus, M ;
Collins, F ;
Shiloh, Y ;
Crawley, JN ;
Ried, T ;
Tagle, D ;
WynshawBoris, A .
CELL, 1996, 86 (01) :159-171
[3]   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
[4]   Role of the human RAD51 protein in homologous recombination and double-stranded break repair [J].
Baumann, P ;
West, SC .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (07) :247-251
[5]   The breast cancer susceptibility gene BRCA1 is required for subnuclear assembly of Rad51 and survival following treatment with the DNA cross-linking agent cisplatin [J].
Bhattacharyya, A ;
Ear, US ;
Koller, BH ;
Weichselbaum, RR ;
Bishop, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23899-23903
[6]   Xrcc3 is required for assembly of Rad51 complexes in vivo [J].
Bishop, DK ;
Ear, U ;
Bhattacharyya, A ;
Calderone, C ;
Beckett, M ;
Weichselbaum, RR ;
Shinohara, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21482-21488
[7]   Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouse [J].
Blunt, T ;
Gell, D ;
Fox, M ;
Taccioli, GE ;
Lehmann, AR ;
Jackson, SP ;
Jeggo, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10285-10290
[8]   DNA double-strand breaks in immunoglobulin genes undergoing somatic hypermutation [J].
Bross, L ;
Fukita, Y ;
McBlane, F ;
Démollière, C ;
Rajewsky, K ;
Jacobs, H .
IMMUNITY, 2000, 13 (05) :589-597
[9]   Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation [J].
Connor, F ;
Bertwistle, D ;
Mee, PJ ;
Ross, GM ;
Swift, S ;
Grigorieva, E ;
Tybulewicz, VLJ ;
Ashworth, A .
NATURE GENETICS, 1997, 17 (04) :423-430
[10]  
Cooper MP, 2000, GENE DEV, V14, P907