Repair of oxidative DNA base lesions induced by fluorescent light is defective in xeroderma pigmentosum group A cells

被引:39
|
作者
Lipinski, LJ
Hoehr, N
Mazur, SJ
Dianov, GL
Sentürker, S
Dizdaroglu, M
Bohr, VA [1 ]
机构
[1] NIA, Mol Genet Lab, NIH, Baltimore, MD 21224 USA
[2] Natl Inst Stand & Technol, Chem Sci & Technol Lab, Gaithersburg, MD 20899 USA
关键词
D O I
10.1093/nar/27.15.3153
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
Fluorescent light (FL) has been shown to generate free radicals within cells, however, the specific chemical nature of DNA damage induced by FL has not previously been determined. Using gas chromatography/isotope dilution mass spectrometry, we have detected induction of the oxidative DNA lesions 5-hydroxycytosine (5-OH-Cyt), 2,6-diamino-4-hydroxy-5-formamidopyrimidine (FapyGua) and 4,6-diamino-5-formamidopyrimidine (FapyAde) in cultured cells irradiated with FL, We followed the repair of these lesions in normal and xeroderma pigmentosum group A (XP-A) cells. 5-OH-Cyt and FapyGua were repaired efficiently in normal cells within 6 h following FL exposure. XP-A cells were unable to repair these oxidative DNA base lesions. Additionally, to compare the repair of oxidative lesions induced by various sources, in vitro repair studies were performed using plasmid DNA damaged by FL, gamma-irradiation or OsO4 treatment. Whole cell extracts from normal cells repaired damaged substrates efficiently, whereas there was little repair in XP-A extracts, Our data demonstrate defective repair of oxidative DNA base lesions in XP-A cells in vivo and in vitro.
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页码:3153 / 3158
页数:6
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