Literature DB >> 20483371

8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress.

Zsolt Radak1, Istvan Boldogh.   

Abstract

The one-electron oxidation product of guanine, 8-oxo-7,8-dihydroguanine (8-oxoG), is an abundant lesion in genomic, mitochondrial, and telomeric DNA and RNA. It is considered to be a marker of oxidative stress that preferentially accumulates at the 5' end of guanine strings in the DNA helix, in guanine quadruplexes, and in RNA molecules. 8-OxoG has a lower oxidation potential compared to guanine; thus it is susceptible to oxidation/reduction and, along with its redox products, is traditionally considered to be a major mutagenic DNA base lesion. It does not change the architecture of the DNA double helix and it is specifically recognized and excised by 8-oxoguanine DNA glycosylase (OGG1) during the DNA base excision repair pathway. OGG1 null animals accumulate excess levels of 8-oxoG in their genome, yet they do not have shorter life span nor do they exhibit severe pathological symptoms including tumor formation. In fact they are increasingly resistant to inflammation. Here we address the rarely considered significance of 8-oxoG, such as its optimal levels in DNA and RNA under a given condition, essentiality for normal cellular physiology, evolutionary role, and ability to soften the effects of oxidative stress in DNA, and the harmful consequences of its repair, as well as its importance in transcriptional initiation and chromatin relaxation. Copyright (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20483371      PMCID: PMC2943936          DOI: 10.1016/j.freeradbiomed.2010.05.008

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  207 in total

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  54 in total

1.  Biochemical identification of a hydroperoxide derivative of the free 8-oxo-7,8-dihydroguanine base.

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3.  8-Oxoguanine DNA glycosylase-1-mediated DNA repair is associated with Rho GTPase activation and α-smooth muscle actin polymerization.

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Review 6.  Inside-Out Signaling Pathways from Nuclear Reactive Oxygen Species Control Pulmonary Innate Immunity.

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7.  Age-dependent changes in 8-oxoguanine-DNA glycosylase activity are modulated by adaptive responses to physical exercise in human skeletal muscle.

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Review 9.  8-Oxoguanine DNA glycosylase-1-driven DNA base excision repair: role in asthma pathogenesis.

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10.  8-Oxoguanine DNA glycosylase-1 links DNA repair to cellular signaling via the activation of the small GTPase Rac1.

Authors:  Gyorgy Hajas; Attila Bacsi; Leopoldo Aguilera-Aguirre; Muralidhar L Hegde; K Hazra Tapas; Sanjiv Sur; Zsolt Radak; Xueqing Ba; Istvan Boldogh
Journal:  Free Radic Biol Med       Date:  2013-04-21       Impact factor: 7.376

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