Is the repair of oxidative DNA base modifications inducible by a preceding DNA damage induction?

被引:12
作者
Bercht, Marc
Flohr-Beckhaus, Claudia
Osterod, Marcel
Runger, Thomas M.
Radicella, J. Pablo
Epe, Bernd
机构
[1] Univ Mainz, Inst Pharm, D-55099 Mainz, Germany
[2] Boston Univ, Dept Dermatol, Boston, MA 02118 USA
[3] CEA, CNRS, UMR 217, Dept Radiobiol & Radiopathol, F-92265 Fontenay Aux Roses, France
关键词
base excision repair; adaptive response; oxidative DNA damage;
D O I
10.1016/j.dnarep.2006.11.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In mammalian cells, 7,8-dihydro-8-oxoguanine (8-oxoG) and some other oxidative guanine modifications are removed from the DNA by base excision repair, which is initiated by OGG1 protein. We have tested whether this repair is inducible in mouse embryonic fibroblasts (MEFs), MCF-7 breast cancer cells and primary human fibroblasts by a pretreatment with the photosensitizer Ro19-8022 plus light, which generates predominantly 8-oxoG, or with methyl methanesulfonate (MMS), which generates alkylated bases and abasic sites (AP sites). The results indicate that the repair rate of the oxidative guanine modifications induced by the photosensitizer was not increased if a priming dose of the oxidative or alkylating agent was applied 6 or 18 h prior to a challenging dose, although pretreatments with both agents resulted in two-fold elevated glutathione levels as an indication for an adaptive response. Similarly, the activity of total protein extracts of the cells to incise at a single 8-oxoG residue in an oligonucleotide was unchanged. it has to be concluded that the repair of 8-oxoG is not inducible by oxidative or alkylation damage. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:367 / 373
页数:7
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