Checkpoint mechanisms at the intersection between DNA damage and repair

被引:71
作者
Lazzaro, Federico [1 ]
Giannattasio, Michele [1 ]
Puddu, Fabio [1 ]
Granata, Magda [1 ]
Pellicioli, Achille [1 ]
Plevani, Paolo [1 ]
Muzi-Falconi, Marco [1 ]
机构
[1] Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
关键词
DNA damage; DNA repair; Checkpoint; Cell cycle; Translesion DNA synthesis; DOUBLE-STRAND-BREAK; NUCLEOTIDE EXCISION-REPAIR; STALLED REPLICATION FORKS; NITRO-N-NITROSOGUANIDINE; CELL-CYCLE CHECKPOINT; MISMATCH-REPAIR; SACCHAROMYCES-CEREVISIAE; BUDDING YEAST; ATAXIA-TELANGIECTASIA; UV-IRRADIATION;
D O I
10.1016/j.dnarep.2009.04.022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In response to genomic insults cells trigger a signal transduction pathway, known as DNA damage checkpoint, whose role is to help the cell to cope with the damage by coordinating cell cycle progression, DNA replication and DNA repair mechanisms. Accumulating evidence suggests that activation of the first checkpoint kinase in the cascade is not due to the lesion itself, but it requires recognition and initial processing of the lesion by a specific repair mechanism. Repair enzymes likely convert a variety of physically and chemically different lesions to a unique common structure, a ssDNA region, which is the checkpoint triggering signal. Checkpoint kinases can modify the activity of repair mechanisms, allowing for efficient repair, on one side, and modulating the generation of the ssDNA signal, on the other. This strategy may be important to allow the most effective repair and a prompt recovery from the damage condition. Interestingly, at least in some cases, if the damage level is low enough the cell can deal with the lesions and it does not need to activate the checkpoint response. On the other hand if damage level is high or if the lesions are not rapidly repairable, checkpoint mechanisms become important for cell survival and preservation of genome integrity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1055 / 1067
页数:13
相关论文
共 170 条
[61]   Phosphorylation of Rad55 on serines 2, 8, and 14 is required for efficient homologous recombination in the recovery of stalled replication forks [J].
Herzberg, Kristina ;
Bashkirov, Vladimir I. ;
Rolfsmeier, Michael ;
Haghnazari, Edwin ;
McDonald, W. Hayes ;
Anderson, Scott ;
Bashkirova, Elena V. ;
Yates, John R., III ;
Heyer, Wolf-Dietrich .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (22) :8396-8409
[62]   ATR homolog Mec1 controls association of DNA polymerase ζ-Rev1 complex with regions near a double-strand break [J].
Hirano, Y ;
Sugimoto, K .
CURRENT BIOLOGY, 2006, 16 (06) :586-590
[63]   RAD6-RAD18-RAD5-pathway-dependent tolerance to chronic low-dose ultraviolet light [J].
Hishida, Takashi ;
Kubota, Yoshino ;
Carr, Antony M. ;
Iwasaki, Hiroshi .
NATURE, 2009, 457 (7229) :612-U124
[64]   RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO [J].
Hoege, C ;
Pfander, B ;
Moldovan, GL ;
Pyrowolakis, G ;
Jentsch, S .
NATURE, 2002, 419 (6903) :135-141
[65]   Genome maintenance mechanisms for preventing cancer [J].
Hoeijmakers, JHJ .
NATURE, 2001, 411 (6835) :366-374
[66]   RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly [J].
Huen, Michael S. Y. ;
Grant, Robert ;
Manke, Isaac ;
Minn, Kay ;
Yu, Xiaochun ;
Yaffe, Michael B. ;
Chen, Junjie .
CELL, 2007, 131 (05) :901-914
[67]   CDK targets Sae2 to control DNA-end resection and homologous recombination [J].
Huertas, Pablo ;
Cortes-Ledesma, Felipe ;
Sartori, Alessandro A. ;
Aguilera, Andres ;
Jackson, Stephen P. .
NATURE, 2008, 455 (7213) :689-U86
[68]   DNA end resection, homologous recombination and DNA damage checkpoint activation require CDK1 [J].
Ira, G ;
Pellicioli, A ;
Balijja, A ;
Wang, X ;
Fiorani, S ;
Carotenuto, W ;
Liberi, G ;
Bressan, D ;
Wan, LH ;
Hollingsworth, NM ;
Haber, JE ;
Foiani, M .
NATURE, 2004, 431 (7011) :1011-1017
[69]   DNA mismatch repair: Functions and mechanisms [J].
Iyer, RR ;
Pluciennik, A ;
Burdett, V ;
Modrich, PL .
CHEMICAL REVIEWS, 2006, 106 (02) :302-323
[70]   ATM- and cell cycle-dependent regulation of ATR in response to DNA double-strand breaks [J].
Jazayeri, A ;
Falck, J ;
Lukas, C ;
Bartek, J ;
Smith, GCM ;
Lukas, J ;
Jackson, SP .
NATURE CELL BIOLOGY, 2006, 8 (01) :37-U13