The response to DNA damage during differentiation: Pathways and consequences

被引:38
作者
Fortini, Paola [1 ]
Ferretti, Chiara [1 ]
Dogliotti, Eugenia [1 ]
机构
[1] Ist Super Sanita, Dept Environm & Primary Prevent, I-00161 Rome, Italy
关键词
DNA repair; DNA damage response; Apoptosis; Autophagy; Cell differentiation; Stem cells; EMBRYONIC STEM-CELLS; DOUBLE-STRAND BREAKS; NUCLEOTIDE EXCISION-REPAIR; SKELETAL-MUSCLE DIFFERENTIATION; HOMOLOGOUS RECOMBINATION; MITOCHONDRIAL BIOGENESIS; SOMATIC-CELLS; SELF-RENEWAL; LIFE-SPAN; CYCLE;
D O I
10.1016/j.mrfmmm.2013.03.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Damage to genomic DNA triggers a prompt set of signaling events known as the DNA damage response (DDR) which coordinates DNA repair, cell cycle arrest and ultimately cell death or senescence. Although activation of adequate DNA damage signaling and repair systems depends on the type of lesion and the cell-cycle phase in which it occurs, emerging evidence indicates that DNA repair and DDR function differently in different cellular contexts. Depending on the time maintenance and function of a specific cell type the risk of accumulating DNA damage may vary. For instance, damage to stem cells if not repaired can lead to mutation amplification or propagation through the processes of self-renewal and differentiation, respectively, whereas damage to post-mitotic cells can affect mostly tissue homeostasis. Stem cells are therefore expected to address DNA damage differently from their somatic counterparts. In this review the information available on the common and distinct mechanisms of control of genome integrity utilized by different cell types along the self-renewal/differentiation program will be reviewed, with special emphasis on their roles in the prevention of aging and disease. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 168
页数:9
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