Christmann Markus, Tomicic Maja T, Roos Wynand P, Kaina Bernd
Division of Applied Toxicology, Institute of Toxicology, University of Mainz, Obere Zahlbacher Str. 67, D-55131 Mainz, Germany.
Toxicology. 2003 Nov 15;193(1-2):3-34. doi: 10.1016/s0300-483x(03)00287-7.
The human genome, comprising three billion base pairs coding for 30000-40000 genes, is constantly attacked by endogenous reactive metabolites, therapeutic drugs and a plethora of environmental mutagens that impact its integrity. Thus it is obvious that the stability of the genome must be under continuous surveillance. This is accomplished by DNA repair mechanisms, which have evolved to remove or to tolerate pre-cytotoxic, pre-mutagenic and pre-clastogenic DNA lesions in an error-free, or in some cases, error-prone way. Defects in DNA repair give rise to hypersensitivity to DNA-damaging agents, accumulation of mutations in the genome and finally to the development of cancer and various metabolic disorders. The importance of DNA repair is illustrated by DNA repair deficiency and genomic instability syndromes, which are characterised by increased cancer incidence and multiple metabolic alterations. Up to 130 genes have been identified in humans that are associated with DNA repair. This review is aimed at updating our current knowledge of the various repair pathways by providing an overview of DNA-repair genes and the corresponding proteins, participating either directly in DNA repair, or in checkpoint control and signaling of DNA damage.
人类基因组由30亿个碱基对组成,编码30000 - 40000个基因,不断受到内源性反应性代谢产物、治疗药物和大量影响其完整性的环境诱变剂的攻击。因此,基因组的稳定性显然必须受到持续监测。这是通过DNA修复机制来实现的,这些机制已经进化到以无差错或在某些情况下易出错的方式去除或耐受细胞毒性前、诱变前和染色体断裂前的DNA损伤。DNA修复缺陷会导致对DNA损伤剂的超敏反应、基因组中突变的积累,最终导致癌症和各种代谢紊乱的发生。DNA修复缺陷和基因组不稳定综合征说明了DNA修复的重要性,这些综合征的特征是癌症发病率增加和多种代谢改变。在人类中已鉴定出多达130个与DNA修复相关的基因。本综述旨在通过概述直接参与DNA修复或参与DNA损伤的检查点控制和信号传导的DNA修复基因及相应蛋白质,更新我们对各种修复途径的现有认识。