Kruchinin Alexander A, Kamzeeva Polina N, Zharkov Dmitry O, Aralov Andrey V, Makarova Alena V
Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilova St., 119334 Moscow, Russia.
National Research Center, Kurchatov Institute, Kurchatov sq. 2, 123182 Moscow, Russia.
Int J Mol Sci. 2024 Jan 22;25(2):1342. doi: 10.3390/ijms25021342.
Numerous studies have shown that oxidative modifications of guanine (7,8-dihydro-8-oxoguanine, 8-oxoG) can affect cellular functions. 7,8-Dihydro-8-oxoadenine (8-oxoA) is another abundant paradigmatic ambiguous nucleobase but findings reported on the mutagenicity of 8-oxoA in bacterial and eukaryotic cells are incomplete and contradictory. Although several genotoxic studies have demonstrated the mutagenic potential of 8-oxoA in eukaryotic cells, very little biochemical and bioinformatics data about the mechanism of 8-oxoA-induced mutagenesis are available. In this review, we discuss dual coding properties of 8-oxoA, summarize historical and recent genotoxicity and biochemical studies, and address the main protective cellular mechanisms of response to 8-oxoA. We also discuss the available structural data for 8-oxoA bypass by different DNA polymerases as well as the mechanisms of 8-oxoA recognition by DNA repair enzymes.
大量研究表明,鸟嘌呤的氧化修饰(7,8 - 二氢 - 8 - 氧代鸟嘌呤,8 - oxoG)会影响细胞功能。7,8 - 二氢 - 8 - 氧代腺嘌呤(8 - oxoA)是另一种丰富的典型模糊核碱基,但关于8 - oxoA在细菌和真核细胞中致突变性的报道结果并不完整且相互矛盾。尽管多项遗传毒性研究已证明8 - oxoA在真核细胞中的诱变潜力,但关于8 - oxoA诱导诱变机制的生化和生物信息学数据却非常少。在本综述中,我们讨论了8 - oxoA的双重编码特性,总结了历史和近期的遗传毒性及生化研究,并阐述了细胞对8 - oxoA反应的主要保护机制。我们还讨论了不同DNA聚合酶绕过8 - oxoA的现有结构数据以及DNA修复酶识别8 - oxoA的机制。