Recent aspects of oxidative DNA damage: Guanine lesions, measurement and substrate specificity of DNA repair glycosylases

被引:78
作者
Cadet, J
Bellon, S
Berger, M
Bourdat, AG
Douki, T
Duarte, V
Frelon, S
Gasparutto, D
Muller, E
Ravanat, JL
Sauvaigo, S
机构
[1] CEA Grenoble, Lab Les Acides Nucl, Serv Chim Inorgan & Biol, F-38054 Grenoble 9, France
[2] CEA Grenoble, Dept Rech Fondamentale Mat Condensee, UMR 5046, F-38054 Grenoble 9, France
关键词
DNA N-glycosylases; mass spectrometry; nucleotide excision repair; 8-oxo-7,8-dihydro-2 '-deoxyguanosine; reactive oxygen species;
D O I
10.1515/BC.2002.100
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
This review discusses recent aspects of oxidation reactions of DNA and model compounds involving mostly .OH radicals, oneelectron transfer process and singlet oxygen (O-1(2)). Emphasis is placed on the formation of double DNA lesions involving a purine base on one hand and either a pyrimidine base or a 2-deoxyribose moiety on the other hand. Structural and mechanistic information is also provided on secondary oxidation reactions of 8-oxo-7,8-dihydro-2deoxyguanosine (8- oxodGuo), a major DNA marker of oxidative stress. Another major topic which is addressed here deals with recent developments in the measurement of oxidative base damage to cellular DNA. This has been mostly achieved using the accurate and highly specific HPLC method coupled with the tandem mass spectrometry detection technique. Interestingly, optimized conditions of DNA extraction and subsequent workup allow the accurate measurement of 11 modified nucleosides and bases within cellular DNA upon exposure to oxidizing agents, including UVA and ionizing radiations. In addition, the modified comet assay, which involves the use of bacterial DNA Nglycosylases to reveal two main classes of oxidative base damage, is applicable to isolated cells and is particularly suitable when only small amounts of biological material are available. Finally, recently available data on the substrate specificity of DNA repair enzymes belonging to the base excision pathways are briefly reviewed.
引用
收藏
页码:933 / 943
页数:11
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