Literature DB >> 10526220

Oxidative DNA damage and mutations induced by a polar photosensitizer, Ro19-8022.

O Will1, E Gocke, I Eckert, I Schulz, M Pflaum, H C Mahler, B Epe.   

Abstract

The oxidative DNA damage induced by the polar photosensitizer Ro19-8022 in the presence of light was studied and correlated with the associated mutagenicity. Both in isolated DNA and AS52 Chinese hamster ovary cells, photoexcited Ro19-8022 gave rise to a DNA damage profile that was similar to that caused by singlet oxygen: base modifications sensitive to the repair endonuclease Fpg protein, which according to high-performance liquid chromatography (HPLC) analysis were predominantly 8-hydroxyguanine (8-oxoG) residues, were generated in much higher yield than single-strand breaks, sites of base loss (AP sites) and oxidative pyrimidine modifications sensitive to endonuclease III. Fifty percent of the Fpg-sensitive modifications were repaired within 2 h. Under conditions that induced 10 Fpg-sensitive modifications per 10(6) bp (six 8-oxoG residues per 10(6) bp), approximately 60 mutations per 10(6) cells were induced in the gpt locus of the AS52 cells. A rather similar mutation frequency was observed when a plasmid carrying the gpt gene was exposed to Ro19-8022 plus light under cell-free conditions and subsequently replicated in bacteria. Sequence analysis revealed that GC-->TA and GC-->CG transversions accounted for 90% of the base substitutions. A significant generation of micronuclei was detectable in AS52 cells exposed to the photosensitizer plus light as well.

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Year:  1999        PMID: 10526220     DOI: 10.1016/s0921-8777(99)00039-7

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  17 in total

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Review 2.  Micro-irradiation tools to visualize base excision repair and single-strand break repair.

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6.  Limited repair of 8-hydroxy-7,8-dihydroguanine residues in human testicular cells.

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7.  Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress.

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8.  Newly identified CHO ERCC3/XPB mutations and phenotype characterization.

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9.  A ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repair.

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10.  An ECVAG trial on assessment of oxidative damage to DNA measured by the comet assay.

Authors:  Clara Johansson; Peter Møller; Lykke Forchhammer; Steffen Loft; Roger W L Godschalk; Sabine A S Langie; Stijn Lumeij; George D D Jones; Rachel W L Kwok; Amaya Azqueta; David H Phillips; Osman Sozeri; Michael N Routledge; Alexander J Charlton; Patrizia Riso; Marisa Porrini; Alessandra Allione; Giuseppe Matullo; Jadwiga Palus; Maciej Stepnik; Andrew R Collins; Lennart Möller
Journal:  Mutagenesis       Date:  2009-11-30       Impact factor: 3.000

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