Record number :
1304235
Title of article :
DNA polymerase bypass in vitro and in E. coli of a C-nucleotide analogue of Fapy·dG Original Research Article
Author/Authors :
Yvonne N. Weledji، نويسنده , , Carissa J. Wiederholt، نويسنده , , Michael O. Delaney، نويسنده , , Marc M. Greenberg، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
6
From page :
4029
To page :
4034
Abstract :
Bypass of the configurationally stable analogue (β-C-Fapy·dG) of the formamidopyrimidine lesion derived from 2′-deoxyguanosine oxidation (Fapy·dG) was studied in vitro and in Escherichia coli. The exonuclease deficient Klenow fragment of E. coli DNA polymerase I (Klenow exo−) misincorporated dA most frequently opposite β-C-Fapy·dG, but its efficiency was <0.2% of dC insertion. Klenow exo− fidelity was enhanced by the enzyme’s high selectivity for extending duplexes only when dC was opposite β-C-Fapy·dG. The expectations raised by these in vitro data were realized when β-C-Fapy·dG replication was studied in E. coli by transfecting M13mp7(L2) bacteriophage DNA containing the nucleotide analogue within the lacZ gene in 4 local sequence contexts. The bypass efficiency of β-C-Fapy·dG varied between 45% and 70% compared to a genome containing only native nucleotides. Mutation frequencies at the site of the lesions in the originally transfected genomes were determined using the REAP assay [Delaney, J. C.; Essigmann, J. M. Methods Enzymol. 2006, 408, 1]. The levels of mutations could not be distinguished between those observed when genomes containing native nucleotides were replicated, indicating that the mutagenicity of β-C-Fapy·dG was <1%. These data and previous reports indicate that β-C-Fapy·dG is a good model of Fapy·dG in E. coli. In addition, these results and the previous report of β-C-Fapy·dG binding to the base excision repair protein formamidopyrimidine glycosylase suggest that this analogue could be useful as a DNA repair inhibitor.
Keywords :
DNA lesions , DNA damage , Modified nucleotides , DNA replication
Journal title :
Bioorganic and Medicinal Chemistry
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Link To Document :
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