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Identification of ultimate DNA damaging oxygen species.

DNA damage induced by various reactive oxygen species can be characterized using a set of repair endonucleases with defined substrate specificities. DNA damage profiles thus obtained in a cell-free system can be compared with those observed in cellular DNA. Using this approach, we have demonstrated...

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Detalles Bibliográficos
Autores principales: Epe, B, Hegler, J, Wild, D
Formato: Texto
Lenguaje:English
Publicado: 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1567987/
https://www.ncbi.nlm.nih.gov/pubmed/2272304
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author Epe, B
Hegler, J
Wild, D
author_facet Epe, B
Hegler, J
Wild, D
author_sort Epe, B
collection PubMed
description DNA damage induced by various reactive oxygen species can be characterized using a set of repair endonucleases with defined substrate specificities. DNA damage profiles thus obtained in a cell-free system can be compared with those observed in cellular DNA. Using this approach, we have demonstrated that an illumination of Salmonella typhimurium cells with visible light in the presence of methylene blue gives rise to a DNA damage profile very similar to that of singlet oxygen in a cell-free system. Therefore, the genotoxicity observed under these conditions most probably is attributable to the direct action of this species. The damage consists mainly of base modifications that are subject to repair by uvrABC-independent pathways. Revertant frequencies observed in parallel in the strains TA100 and TA2638 indicate a pronounced mutagenicity of the lesions induced. Exposure of Salmonella typhimurium to tert-butylhydroperoxide gives rise to another form of damage profile that is also different from that produced by hydroxyl radicals in a cell-free system. However, the latter dissimilarity does not exclude hydroxyl radicals as ultimate reactive species, as a very rapid repair of the induced base modifications is observed, which might have distorted the damage profile despite immediate work up.
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spelling pubmed-15679872006-09-18 Identification of ultimate DNA damaging oxygen species. Epe, B Hegler, J Wild, D Environ Health Perspect Research Article DNA damage induced by various reactive oxygen species can be characterized using a set of repair endonucleases with defined substrate specificities. DNA damage profiles thus obtained in a cell-free system can be compared with those observed in cellular DNA. Using this approach, we have demonstrated that an illumination of Salmonella typhimurium cells with visible light in the presence of methylene blue gives rise to a DNA damage profile very similar to that of singlet oxygen in a cell-free system. Therefore, the genotoxicity observed under these conditions most probably is attributable to the direct action of this species. The damage consists mainly of base modifications that are subject to repair by uvrABC-independent pathways. Revertant frequencies observed in parallel in the strains TA100 and TA2638 indicate a pronounced mutagenicity of the lesions induced. Exposure of Salmonella typhimurium to tert-butylhydroperoxide gives rise to another form of damage profile that is also different from that produced by hydroxyl radicals in a cell-free system. However, the latter dissimilarity does not exclude hydroxyl radicals as ultimate reactive species, as a very rapid repair of the induced base modifications is observed, which might have distorted the damage profile despite immediate work up. 1990-08 /pmc/articles/PMC1567987/ /pubmed/2272304 Text en
spellingShingle Research Article
Epe, B
Hegler, J
Wild, D
Identification of ultimate DNA damaging oxygen species.
title Identification of ultimate DNA damaging oxygen species.
title_full Identification of ultimate DNA damaging oxygen species.
title_fullStr Identification of ultimate DNA damaging oxygen species.
title_full_unstemmed Identification of ultimate DNA damaging oxygen species.
title_short Identification of ultimate DNA damaging oxygen species.
title_sort identification of ultimate dna damaging oxygen species.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1567987/
https://www.ncbi.nlm.nih.gov/pubmed/2272304
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