Literature DB >> 10766873

Accumulation of adenine DNA glycosylase-sensitive sites in human mitochondrial DNA.

K Miyako1, C Takamatsu, S Umeda, T Tajiri, M Furuichi, Y Nakabeppu, M Sekiguchi, N Hamasaki, K Takeshige, D Kang.   

Abstract

The mitochondrial respiratory chain inevitably produces reactive oxygen species as byproducts of aerobic ATP synthesis. Mitochondrial DNA (mtDNA), which is located close to the respiratory chain, is reported to contain much more 8-oxoguanine (8-oxoG), an oxidatively modified guanine base, than nuclear DNA. Despite such a high amount of 8-oxoG in mtDNA (1-2 8-oxoG/10(4) G), mtDNA is barely cleaved by an 8-oxoG DNA glycosylase or MutM, which specifically excises 8-oxoG from a C:8-oxoG pair. We find here that about half of human mtDNA molecules are cleaved by another 8-oxoG-recognizing enzyme, an adenine DNA glycosylase or MutY, which excises adenine from an A:8-oxoG pair. The cleavage sites are mapped to adenines. The calculated number of MutY-sensitive sites in mtDNA is approximately 1.4/10(4) G. This value roughly corresponds with the electrochemically measured amount of 8-oxoG in mtDNA (2.2/10(4) G), raising the possibility that 8-oxoG mainly accumulates as an A:8-oxoG pair.

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Year:  2000        PMID: 10766873     DOI: 10.1074/jbc.275.16.12326

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  3 in total

1.  Two distinct pathways of cell death triggered by oxidative damage to nuclear and mitochondrial DNAs.

Authors:  Sugako Oka; Mizuki Ohno; Daisuke Tsuchimoto; Kunihiko Sakumi; Masato Furuichi; Yusaku Nakabeppu
Journal:  EMBO J       Date:  2008-01-10       Impact factor: 11.598

2.  A functional analysis of the DNA glycosylase activity of mouse MUTYH protein excising 2-hydroxyadenine opposite guanine in DNA.

Authors:  Yasuhiro Ushijima; Yohei Tominaga; Tomofumi Miura; Daisuke Tsuchimoto; Kunihiko Sakumi; Yusaku Nakabeppu
Journal:  Nucleic Acids Res       Date:  2005-01-28       Impact factor: 16.971

3.  MUTYH DNA glycosylase: the rationale for removing undamaged bases from the DNA.

Authors:  Enni Markkanen; Julia Dorn; Ulrich Hübscher
Journal:  Front Genet       Date:  2013-02-28       Impact factor: 4.599

  3 in total

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