Chemistry of ROS-mediated oxidation to the guanine base in DNA and its biological consequences

Purpose One outcome of DNA damage from hydroxyl radical generated by ionizing radiation (IR) or by the Fenton reaction is oxidation of the nucleobases, especially guanine (G). While 8-oxo-7,8-dihydroguanine (OG) is a commonly studied oxidized lesion, several others are formed in high abundance, including 5-carboxamido-5-formamido-2-iminohydantoin (2Ih), a prevalent product in in vitro chemistry that is challenging to study from cellular sources. In this short review, we have a goal of explaining new insights into hydroxyl radical-induced oxidation chemistry of G in DNA and comparing it to endogenous DNA damage, as well as commenting on the biological outcomes of DNA base damage. Conclusions Pathways of oxidation of G are discussed and a comparison is made between IR (hydroxyl radical chemistry) and endogenous oxidative stress that largely forms carbonate radical anion as a reactive intermediate. These pathways overlap with the formation of OG and 2Ih, but other guanine-derived lesions are more pathway specific. The biological consequences of guanine oxidation include both mutagenesis and epigenetics; a new mechanism of gene regulation via the base excision repair pathway is described for OG, whereas the impact of IR in forming guanine modifications may be to confound this process in addition to introduction of mutagenic sites.

Automated summary

The article discusses the oxidation of guanine in DNA caused by ionizing radiation or the Fenton reaction, focusing on the formation of various oxidized lesions including 8-oxo-7,8-dihydroguanine (OG) and 5-carboxamido-5-formamido-2-iminohydantoin (2Ih). It compares the pathways and biological consequences of guanine oxidation induced by hydroxyl radicals with endogenous oxidative stress, emphasizing the potential impact on mutagenesis and epigenetics.