Base excision repair deficient mice lacking the Aag alkyladenine DNA glycosylase

被引:204
作者
Engelward, BP
Weeda, G
Wyatt, MD
Broekhof, JLM
deWit, J
Donker, I
Allan, JM
Gold, B
Hoeijmakers, JHJ
Samson, LD
机构
[1] HARVARD UNIV, SCH PUBL HLTH, DEPT MOL & CELLULAR TOXICOL, BOSTON, MA 02115 USA
[2] ERASMUS UNIV ROTTERDAM, DEPT CELL BIOL & GENET, NL-3000 DR ROTTERDAM, NETHERLANDS
[3] UNIV NEBRASKA, MED CTR, EPPLEY INST RES CANC & ALLIED DIS, OMAHA, NE 68198 USA
[4] UNIV NEBRASKA, MED CTR, DEPT PHARMACEUT SCI, OMAHA, NE 68198 USA
关键词
D O I
10.1073/pnas.94.24.13087
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
3-methyladenine (3MeA) DNA glycosylases remove 3MeAs from alkylated DNA to initiate the base excision repair pathway, Here we report the generation of mice deficient in the 3MeA DNA glycosylase encoded by the Aag (Mpg) gene. Alkyladenine DNA glycosylase turns out to be the major DNA glycosylase not only for the cytotoxic 3MeA DNA lesion, but also for the mutagenic 1,N-6-ethenoadenine (epsilon A) and hypoxanthine lesions. Aag appears to be the only 3MeA and hypoxanthine DNA glycosylase in liver, testes, kidney, and lung, and the only epsilon A DNA glycosylase in liver, testes, and kidney; another epsilon A DNA glycosylase may be expressed in lung. Although alkyladenine DNA glycosylase has the capacity to remove 8 oxoguanine DNA lesions, it does not appear to be the major glycosylase for 8-oxoguanine repair, Fibroblasts derived from Aag -/- mice are alkylation sensitive, indicating that Aag -/- mice may be similarly sensitive.
引用
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页码:13087 / 13092
页数:6
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