Kinetics of O6-pyridyloxobutyl-2′-deoxyguanosine repair by human O6-alkylguanine DNA alkyltransferase

Delshanee Kotandeniya, Daniel Murphy, Shuo Yan, Soobong Park, Uthpala Seneviratne, Joseph S. Koopmeiners, Anthony Pegg, Sreenivas Kanugula, Fekadu Kassie, Natalia Tretyakova

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8 Citations (SciVal)


Tobacco-specific nitrosamines 4-(methylnitrosamino)-1-(3-pyridyl)-1- butanone (NNK) and N-nitrosonicotine (NNN) are potent carcinogens believed to contribute to the development of lung tumors in smokers. NNK and NNN are metabolized to DNA-reactive species that form a range of nucleobase adducts, including bulky O6-[4-oxo-4-(3-pyridyl)but-1-yl]deoxyguanosine (O6-POB-dG) lesions. If not repaired, O6-POB-dG adducts induce large numbers of G → A and G → T mutations. Previous studies have shown that O6-POB-dG can be directly repaired by O 6-alkylguanine-DNA alkyltransferase (AGT), which transfers the pyridyloxobutyl group from O6-alkylguanines in DNA to an active site cysteine residue within the protein. In the present study, we investigated the influence of DNA sequence context and endogenous cytosine methylation on the kinetics of AGT-dependent repair of O6-POB-dG in duplex DNA. Synthetic oligodeoxynucleotide duplexes containing site-specific O 6-POB-dG adducts within K-ras and p53 gene-derived DNA sequences were incubated with recombinant human AGT protein, and the kinetics of POB group transfer was monitored by isotope dilution HPLC-ESI+-MS/MS analysis of O6-POB-dG remaining in DNA over time. We found that the second-order rates of AGT-mediated repair were influenced by DNA sequence context (10-fold differences) but were only weakly affected by the methylation status of neighboring cytosines. Overall, AGT-mediated repair of O 6-POB-dG was 2-7 times slower than that of O6-Me-dG adducts. To evaluate the contribution of AGT to O6-POB-dG repair in human lung, normal human bronchial epithelial cells (HBEC) were treated with model pyridyloxobutylating agent, and O6-POB-dG adduct repair over time was monitored by HPLC-ESI+-MS/MS. We found that HBEC cells were capable of removing O6-POB-dG lesions, and the repair rates were significantly reduced in the presence of an AGT inhibitor (O6- benzylguanine). Taken together, our results suggest that AGT plays an important role in protecting human lung against tobacco nitrosamine-mediated DNA damage and that inefficient AGT repair of O6-POB-dG at a specific sequences contributes to mutational spectra observed in smoking-induced lung cancer.

Original languageEnglish (US)
Pages (from-to)4075-4088
Number of pages14
Issue number23
StatePublished - Jun 11 2013

All Science Journal Classification (ASJC) codes

  • Biochemistry


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