DNA repair activity of 8-oxoguanine DNA glycosylase 1 (OGG1) in human lymphocytes is not dependent on genetic polymorphism Ser326/Cys326

被引:110
作者
Janssen, K
Schlink, K
Götte, W
Hippler, B
Kaina, B
Oesch, F
机构
[1] Univ Mainz, Div Appl Toxicol, D-55131 Mainz, Germany
[2] Univ Mainz, Inst Toxicol, D-55131 Mainz, Germany
来源
MUTATION RESEARCH-DNA REPAIR | 2001年 / 486卷 / 03期
关键词
DNA repair; 7,8-dihydro-8-oxoguanine; human OGG1; genetic polymorphism; lymphocytes;
D O I
10.1016/S0921-8777(01)00096-9
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
8-Oxoguanine DNA glycosylase 1 (OGG1) is a DNA repair enzyme that excises 7,8-dihydro-8-oxoguanine (8oxoG) from DNA. Since 8oxoG is a highly mispairing lesion, decreased OGG1 expression level could lead to a higher background mutation frequency and could possibly increase the cancer risk of an individual under oxidative stress. In order to analyse the natural variation of OGG1, we measured the DNA repair activity in human lymphocytes of healthy individuals by means of an 8oxoG-containing oligonucleotide assay. The data obtained revealed a two fold interindividual variation of OGG1 activity in lymphocytes. There was no difference in OGG1 activity due to gender and smoking behaviour. Transcriptional analyses of OGG1 showed the expression of two isoforms, la and b, in lymphocytes. Structural analysis of the human OGG1 (hOGG1) gene revealed a Ser(326)/Cys(326) polymorphism in the Caucasian population with allele frequencies of 75% for Ser(326) and 25% for Cys(326). This polymorphism was not associated with altered OGG1 activity. The described routine test system for measuring OGG1 activity in cryopreserved lymphocytes provided highly reproducible results and is a useful tool for risk assessment associated with alterations in the repair of oxidative DNA damage. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:207 / 216
页数:10
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