TY - JOUR
T1 - Molecular mechanisms of DNA double-strand break repair
AU - Kanaar, Roland
AU - Hoeijmakers, Jan H.J.
AU - Van Gent, Dik C.
N1 - Funding Information:
We apologize to many authors for the omission of their references owing to restriction in reference numbers. We are grateful to J. H. J. Petrini for providing Fig. 3 . The work on DSB repair in our department is supported by grants from the Netherlands Organization for Scientific Research (NWO), the Dutch Cancer Society (KWF), the European Commission and the Human Frontier Science Program Organization. R. K. and D. C. v. G are fellows of the Royal Netherlands Academy of Arts and Sciences.
PY - 1998/12/1
Y1 - 1998/12/1
N2 - DNA double-strand breaks (DSBs) are major threats to the genomic integrity of cells. If not taken care of properly, they can cause chromosome fragmentation, loss and translocation, possibly resulting in carcinogenesis. Upon DSB formation, cell-cycle checkpoints are triggered and multiple DSB repair pathways can be activated. Recent research on the Nijmegen breakage syndrome, which predisposes patients to cancer, suggests a direct link between activation of cell-cycle checkpoints and DSB repair. Furthermore, the biochemical activities of proteins involved in the two major DSB repair pathways, homologous recombination and DNA end-joining, are now beginning to emerge. This review discusses these new findings and their implications for the mechanisms of DSB repair.
AB - DNA double-strand breaks (DSBs) are major threats to the genomic integrity of cells. If not taken care of properly, they can cause chromosome fragmentation, loss and translocation, possibly resulting in carcinogenesis. Upon DSB formation, cell-cycle checkpoints are triggered and multiple DSB repair pathways can be activated. Recent research on the Nijmegen breakage syndrome, which predisposes patients to cancer, suggests a direct link between activation of cell-cycle checkpoints and DSB repair. Furthermore, the biochemical activities of proteins involved in the two major DSB repair pathways, homologous recombination and DNA end-joining, are now beginning to emerge. This review discusses these new findings and their implications for the mechanisms of DSB repair.
UR - http://www.scopus.com/inward/record.url?scp=0031794286&partnerID=8YFLogxK
U2 - 10.1016/S0962-8924(98)01383-X
DO - 10.1016/S0962-8924(98)01383-X
M3 - Review article
C2 - 9861670
AN - SCOPUS:0031794286
SN - 0962-8924
VL - 8
SP - 483
EP - 489
JO - Trends in Cell Biology
JF - Trends in Cell Biology
IS - 12
ER -