Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA

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Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA. / Luxford, C; Morin, B; Dean, R T; Davies, Michael Jonathan.

In: Biochemical Journal, Vol. 344 Pt 1, 15.11.1999, p. 125-34.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Luxford, C, Morin, B, Dean, RT & Davies, MJ 1999, 'Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA', Biochemical Journal, vol. 344 Pt 1, pp. 125-34.

APA

Luxford, C., Morin, B., Dean, R. T., & Davies, M. J. (1999). Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA. Biochemical Journal, 344 Pt 1, 125-34.

Vancouver

Luxford C, Morin B, Dean RT, Davies MJ. Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA. Biochemical Journal. 1999 Nov 15;344 Pt 1:125-34.

Author

Luxford, C ; Morin, B ; Dean, R T ; Davies, Michael Jonathan. / Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA. In: Biochemical Journal. 1999 ; Vol. 344 Pt 1. pp. 125-34.

Bibtex

@article{71c4d124fea048be824acb1f6906a9f1,
title = "Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA",
abstract = "Exposure of amino acids, peptides and proteins to radicals, in the presence of oxygen, gives high yields of hydroperoxides. These materials are readily decomposed by transition metal ions to give further radicals. We hypothesized that hydroperoxide formation on nuclear proteins, and subsequent decomposition of these hydroperoxides to radicals, might result in oxidative damage to associated DNA. We demonstrate here that exposure of histone H1 and model compounds to gamma-radiation in the presence of oxygen gives hydroperoxides in a dose-dependent manner. These hydroperoxides decompose to oxygen- and carbon-centred radicals (detected by electron paramagnetic resonance spectroscopy) on exposure to Cu(+) and other transition metal ions. These hydroperoxide-derived radicals react readily with pyrimidine DNA bases and nucleosides to give adduct species (i.e. protein-DNA base cross-links). Product analysis has demonstrated that radicals from histone H1-hydroperoxides, and other protein and amino acid hydroperoxides, can also oxidize both free 2'-deoxyguanosine and intact calf thymus DNA to give the mutagenic oxidized base 7, 8-dihydro-8-oxo-2'-deoxyguanosine (8-hydroxy-2'-deoxyguanosine, 8-oxodG). The yield of 7,8-dihydro-8-oxo-2'-deoxyguanosine is proportional to the initial protein-hydroperoxide concentration, and corresponds (for histone H1-hydroperoxide, 280 microM) to approx. 1. 4{\%} conversion for free 2'-deoxyguanosine (200 microM), and 0.14{\%} for 2'-deoxyguanosine in DNA (70 microgram/ml). Evidence has also been obtained with DNA for reaction at cytosine and thymine, but not adenine; the lack of damage to the latter may result from damage transfer to 2'-deoxyguanosine residues. These studies demonstrate that initial radical-induced damage to nuclear proteins can give rise to subsequent DNA damage; the latter includes both DNA-protein cross-links and formation of oxidized DNA bases.",
keywords = "Amino Acids, Animals, Cattle, DNA, DNA Damage, Deoxyguanosine, Electron Spin Resonance Spectroscopy, Free Radicals, Histones, Hydrogen Peroxide, In Vitro Techniques, Lysine, Melitten, Oxidation-Reduction, Proteins",
author = "C Luxford and B Morin and Dean, {R T} and Davies, {Michael Jonathan}",
year = "1999",
month = "11",
day = "15",
language = "English",
volume = "344 Pt 1",
pages = "125--34",
journal = "Biochemical Journal",
issn = "0264-6021",
publisher = "Portland Press Ltd.",

}

RIS

TY - JOUR

T1 - Histone H1- and other protein- and amino acid-hydroperoxides can give rise to free radicals which oxidize DNA

AU - Luxford, C

AU - Morin, B

AU - Dean, R T

AU - Davies, Michael Jonathan

PY - 1999/11/15

Y1 - 1999/11/15

N2 - Exposure of amino acids, peptides and proteins to radicals, in the presence of oxygen, gives high yields of hydroperoxides. These materials are readily decomposed by transition metal ions to give further radicals. We hypothesized that hydroperoxide formation on nuclear proteins, and subsequent decomposition of these hydroperoxides to radicals, might result in oxidative damage to associated DNA. We demonstrate here that exposure of histone H1 and model compounds to gamma-radiation in the presence of oxygen gives hydroperoxides in a dose-dependent manner. These hydroperoxides decompose to oxygen- and carbon-centred radicals (detected by electron paramagnetic resonance spectroscopy) on exposure to Cu(+) and other transition metal ions. These hydroperoxide-derived radicals react readily with pyrimidine DNA bases and nucleosides to give adduct species (i.e. protein-DNA base cross-links). Product analysis has demonstrated that radicals from histone H1-hydroperoxides, and other protein and amino acid hydroperoxides, can also oxidize both free 2'-deoxyguanosine and intact calf thymus DNA to give the mutagenic oxidized base 7, 8-dihydro-8-oxo-2'-deoxyguanosine (8-hydroxy-2'-deoxyguanosine, 8-oxodG). The yield of 7,8-dihydro-8-oxo-2'-deoxyguanosine is proportional to the initial protein-hydroperoxide concentration, and corresponds (for histone H1-hydroperoxide, 280 microM) to approx. 1. 4% conversion for free 2'-deoxyguanosine (200 microM), and 0.14% for 2'-deoxyguanosine in DNA (70 microgram/ml). Evidence has also been obtained with DNA for reaction at cytosine and thymine, but not adenine; the lack of damage to the latter may result from damage transfer to 2'-deoxyguanosine residues. These studies demonstrate that initial radical-induced damage to nuclear proteins can give rise to subsequent DNA damage; the latter includes both DNA-protein cross-links and formation of oxidized DNA bases.

AB - Exposure of amino acids, peptides and proteins to radicals, in the presence of oxygen, gives high yields of hydroperoxides. These materials are readily decomposed by transition metal ions to give further radicals. We hypothesized that hydroperoxide formation on nuclear proteins, and subsequent decomposition of these hydroperoxides to radicals, might result in oxidative damage to associated DNA. We demonstrate here that exposure of histone H1 and model compounds to gamma-radiation in the presence of oxygen gives hydroperoxides in a dose-dependent manner. These hydroperoxides decompose to oxygen- and carbon-centred radicals (detected by electron paramagnetic resonance spectroscopy) on exposure to Cu(+) and other transition metal ions. These hydroperoxide-derived radicals react readily with pyrimidine DNA bases and nucleosides to give adduct species (i.e. protein-DNA base cross-links). Product analysis has demonstrated that radicals from histone H1-hydroperoxides, and other protein and amino acid hydroperoxides, can also oxidize both free 2'-deoxyguanosine and intact calf thymus DNA to give the mutagenic oxidized base 7, 8-dihydro-8-oxo-2'-deoxyguanosine (8-hydroxy-2'-deoxyguanosine, 8-oxodG). The yield of 7,8-dihydro-8-oxo-2'-deoxyguanosine is proportional to the initial protein-hydroperoxide concentration, and corresponds (for histone H1-hydroperoxide, 280 microM) to approx. 1. 4% conversion for free 2'-deoxyguanosine (200 microM), and 0.14% for 2'-deoxyguanosine in DNA (70 microgram/ml). Evidence has also been obtained with DNA for reaction at cytosine and thymine, but not adenine; the lack of damage to the latter may result from damage transfer to 2'-deoxyguanosine residues. These studies demonstrate that initial radical-induced damage to nuclear proteins can give rise to subsequent DNA damage; the latter includes both DNA-protein cross-links and formation of oxidized DNA bases.

KW - Amino Acids

KW - Animals

KW - Cattle

KW - DNA

KW - DNA Damage

KW - Deoxyguanosine

KW - Electron Spin Resonance Spectroscopy

KW - Free Radicals

KW - Histones

KW - Hydrogen Peroxide

KW - In Vitro Techniques

KW - Lysine

KW - Melitten

KW - Oxidation-Reduction

KW - Proteins

M3 - Journal article

C2 - 10548542

VL - 344 Pt 1

SP - 125

EP - 134

JO - Biochemical Journal

JF - Biochemical Journal

SN - 0264-6021

ER -

ID: 138282309