The emerging role of RNAs in DNA damage repair

被引:33
|
作者
Hawley, Ben R. [1 ]
Lu, Wei-Ting [1 ]
Wilczynska, Ania [1 ]
Bushell, Martin [1 ]
机构
[1] MRC Toxicol Unit, Hodgkin Bldg, Leicester LE1 9HN, Leics, England
来源
CELL DEATH AND DIFFERENTIATION | 2017年 / 24卷 / 04期
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
DOUBLE-STRAND BREAK; HOMOLOGY-DIRECTED REPAIR; MAMMALIAN-CELLS; NONCODING RNA; GENOME; RECOMBINATION; POLYMERASE; STABILITY; PATHWAY; INTERFERENCE;
D O I
10.1038/cdd.2017.16
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many surveillance and repair mechanisms exist to maintain the integrity of our genome. All of the pathways described to date are controlled exclusively by proteins, which through their enzymatic activities identify breaks, propagate the damage signal, recruit further protein factors and ultimately resolve the break with little to no loss of genetic information. RNA is known to have an integral role in many cellular pathways, but, until very recently, was not considered to take part in the DNA repair process. Several reports demonstrated a conserved critical role for RNA-processing enzymes and RNA molecules in DNA repair, but the biogenesis of these damage-related RNAs and their mechanisms of action remain unknown. We will explore how these new findings challenge the idea of proteins being the sole participants in the response to DNA damage and reveal a new and exciting aspect of both DNA repair and RNA biology.
引用
收藏
页码:580 / 587
页数:8
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