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Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX

Histone H2AX is a minor component of nuclear histone H2A. The phosphorylation of histone H2AX at Ser 139, termed γ-H2AX, was originally identified as an early event after the direct formation of DNA double-strand breaks (DSBs) by ionizing radiation. Now, the generation of γ-H2AX is also considered t...

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Detalles Bibliográficos
Autores principales: Ibuki, Yuko, Toyooka, Tatsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380052/
https://www.ncbi.nlm.nih.gov/pubmed/25480829
http://dx.doi.org/10.1093/jrr/rru105
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author Ibuki, Yuko
Toyooka, Tatsushi
author_facet Ibuki, Yuko
Toyooka, Tatsushi
author_sort Ibuki, Yuko
collection PubMed
description Histone H2AX is a minor component of nuclear histone H2A. The phosphorylation of histone H2AX at Ser 139, termed γ-H2AX, was originally identified as an early event after the direct formation of DNA double-strand breaks (DSBs) by ionizing radiation. Now, the generation of γ-H2AX is also considered to occur in association with secondarily formed DSBs by cellular processing such as DNA replication and repair at the site of the initial damage, including DNA adducts, crosslinks, and UV-induced photolesions. Therefore, γ-H2AX is currently attracting attention as a new biomarker for detecting various genotoxic insults. We have determined the toxic impact of various environmental stresses such as chemicals, light and/or their coexposure using γ-H2AX, and found that the γ-H2AX assay exhibited high sensitivity and a low false-positive rate as a detection system of genotoxic potential. In this review, we introduced our recent findings concerning the evaluation of chemical phototoxicity, focusing on γ-H2AX.
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spelling pubmed-43800522015-04-15 Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX Ibuki, Yuko Toyooka, Tatsushi J Radiat Res Reviews Histone H2AX is a minor component of nuclear histone H2A. The phosphorylation of histone H2AX at Ser 139, termed γ-H2AX, was originally identified as an early event after the direct formation of DNA double-strand breaks (DSBs) by ionizing radiation. Now, the generation of γ-H2AX is also considered to occur in association with secondarily formed DSBs by cellular processing such as DNA replication and repair at the site of the initial damage, including DNA adducts, crosslinks, and UV-induced photolesions. Therefore, γ-H2AX is currently attracting attention as a new biomarker for detecting various genotoxic insults. We have determined the toxic impact of various environmental stresses such as chemicals, light and/or their coexposure using γ-H2AX, and found that the γ-H2AX assay exhibited high sensitivity and a low false-positive rate as a detection system of genotoxic potential. In this review, we introduced our recent findings concerning the evaluation of chemical phototoxicity, focusing on γ-H2AX. Oxford University Press 2015-03 2014-12-04 /pmc/articles/PMC4380052/ /pubmed/25480829 http://dx.doi.org/10.1093/jrr/rru105 Text en © The Author 2014. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology.
spellingShingle Reviews
Ibuki, Yuko
Toyooka, Tatsushi
Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title_full Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title_fullStr Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title_full_unstemmed Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title_short Evaluation of chemical phototoxicity, focusing on phosphorylated histone H2AX
title_sort evaluation of chemical phototoxicity, focusing on phosphorylated histone h2ax
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380052/
https://www.ncbi.nlm.nih.gov/pubmed/25480829
http://dx.doi.org/10.1093/jrr/rru105
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