Abstract
8-Hydroxyl-2'-deoxyguanosine (also referred to as 8- hydroxyguanine [8-OH-dG] or 7,8-dihydro-8-oxoguanine), a common DNA adduct resulting from injury to DNA via reactive oxygen species, affects the in vitro methylation of nearby cytosine moieties by the human DNA methyltransferase. The exact position of 8-OH-deoxyguanosine relative to a CpG dinucleotide appears important to this effect. Our data indicate that 8-OH-deoxyguanosine diminishes the ability of the methyltransferase to methylate a target cytosine when the 8-OH-deoxyguanosine is one or two nucleotides 3' from the cytosine, on the same strand On the other hand 8-OH-deoxyguanosine does not diminish the ability of the enzyme to respond to a methyl director (5-methylcytosine) when the 8-OH-deoxyguanosine is on the same strand but one or two nucleotides 3' from the methyl director. Differences in methylation rates as great as 13-fold have been detected using various 8-OH-deoxyguanosine-containing oligonucleotides as substrates in methylation assays. Our findings suggest that oxidative damage of parental strand guanines would permit normal copying of methylation patterns through maintenance methylation, while oxidative damage of guanines in the nascent strand DNA would inhibit such methylation.
Original language | English (US) |
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Pages (from-to) | 1253-1255 |
Number of pages | 3 |
Journal | Carcinogenesis |
Volume | 16 |
Issue number | 5 |
DOIs | |
State | Published - May 1995 |
Funding
Supported by a generous grant from The Buehler Center on Aging and by National Institutes of Health grant RO1 AG11536 to S.A.W. and by the Smokeless Tobacco Research Council, Inc. grant 0388 to S.S.S. who is also a member of the Clinical Cancer Center of the City of Hope (CA335762-09).
ASJC Scopus subject areas
- Cancer Research