Enzymatic properties of Escherichia coli and human 7,8-dihydro-8-oxoguanine DNA glycosylases
Author(s) -
Kenjiro Asagoshi,
Takao Yamada,
Hiroaki Terato,
Y. Ohyama,
Hiroshi Ide
Publication year - 2000
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/44.1.11
Subject(s) - oligonucleotide , dna glycosylase , escherichia coli , pyrimidine , dna , chemistry , biochemistry , guanine , enzyme , microbiology and biotechnology , biology , dna repair , nucleotide , gene
Oxidative damage to DNA generates aberrant guanine bases such as 2,6-diamino-4-hydroxy-formamido-pyrimidine (Fapy) and 7,8-dihydro-8-oxoguanine (8-oxoG). Although synthetic oligonucleotides containing a single 8-oxoG have been widely used to study enzymatic processing of this lesion, the synthesis of oligonucleotides containing Fapy as a unique lesion has not been achieved to date. In this study, an oligonucleotide containing a single 2,6-diamino-4-hydroxy-5-(N-methyl)formamido-pyrimidine (me-Fapy, a methylated derivative of Fapy) was prepared by a DNA polymerase reaction and the subsequent alkali treatment. The repair activity of Fpg and hOGG1 proteins were compared using oligonucleotide substrates containing me-Fapy and 8-oxoG.
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