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DNA Damage Response: Three Levels of DNA Repair Regulation
被引:177
|作者:
Sirbu, Bianca M.
[1
]
Cortez, David
[1
]
机构:
[1] Vanderbilt Univ, Sch Med, Dept Biochem, Nashville, TN 37027 USA
来源:
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY
|
2013年
/
5卷
/
08期
关键词:
DOUBLE-STRAND BREAKS;
STALLED REPLICATION FORKS;
CROSS-LINK REPAIR;
DEPENDENT PROTEIN-KINASE;
FANCONI-ANEMIA PATHWAY;
CELL-CYCLE CHECKPOINT;
EARLY EMBRYONIC LETHALITY;
RIBONUCLEOTIDE REDUCTASE;
S-PHASE;
HOMOLOGOUS RECOMBINATION;
D O I:
10.1101/cshperspect.a012724
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Genome integrity is challenged by DNA damage from both endogenous and environmental sources. This damage must be repaired to allow both RNA and DNA polymerases to accurately read and duplicate the information in the genome. Multiple repair enzymes scan the DNA for problems, remove the offending damage, and restore the DNA duplex. These repair mechanisms are regulated by DNA damage response kinases including DNA-PKcs, ATM, and ATR that are activated at DNA lesions. These kinases improve the efficiency of DNA repair by phosphorylating repair proteins to modify their activities, by initiating a complex series of changes in the local chromatin structure near the damage site, and by altering the overall cellular environment to make it more conducive to repair. In this review, we focus on these three levels of regulation to illustrate how the DNA damage kinases promote efficient repair to maintain genome integrity and prevent disease.
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