The DNA Damage Response: Making It Safe to Play with Knives

被引:3985
作者
Ciccia, Alberto [1 ,2 ,3 ]
Elledge, Stephen J. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Genet, Boston, MA 02115 USA
关键词
DOUBLE-STRAND BREAKS; FANCONI-ANEMIA PATHWAY; REPLICATION PROTEIN-A; HOMOLOGOUS RECOMBINATION REPAIR; MAINTAINS GENOMIC STABILITY; CROSS-LINK REPAIR; AMYOTROPHIC-LATERAL-SCLEROSIS; HOLLIDAY JUNCTION RESOLVASE; NUCLEOTIDE EXCISION-REPAIR; CLASS SWITCH RECOMBINATION;
D O I
10.1016/j.molcel.2010.09.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Damage to our genetic material is an ongoing threat to both our ability to faithfully transmit genetic information to our offspring as well as our own survival. To respond to these threats, eukaryotes have evolved the DNA damage response (DDR). The DDR is a complex signal transduction pathway that has the ability to sense DNA damage and transduce this information to the cell to influence cellular responses to DNA damage. Cells possess an arsenal of enzymatic tools capable of remodeling and repairing DNA; however, their activities must be tightly regulated in a temporal, spatial, and DNA lesion-appropriate fashion to optimize repair and prevent unnecessary and potentially deleterious alterations in the structure of DNA during normal cellular processes. This review will focus on how the DDR controls DNA repair and the phenotypic consequences of defects in these critical regulatory functions in mammals.
引用
收藏
页码:179 / 204
页数:26
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