Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131 Naples, Italy.
Department of Biology, University of Naples Federico II, 80138 Naples, Italy.
Int J Mol Sci. 2023 Jan 19;24(3):2031. doi: 10.3390/ijms24032031.
The guanine base in nucleic acids is, among the other bases, the most susceptible to being converted into 8-Oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) when exposed to reactive oxygen species. In double-helix DNA, 8-oxodG can pair with adenine; hence, it may cause a G > T (C > A) mutation; it is frequently referred to as a form of DNA damage and promptly corrected by DNA repair mechanisms. Moreover, 8-oxodG has recently been redefined as an epigenetic factor that impacts transcriptional regulatory elements and other epigenetic modifications. It has been proposed that 8-oxodG exerts epigenetic control through interplay with the G-quadruplex (G4), a non-canonical DNA structure, in transcription regulatory regions. In this review, we focused on the epigenetic roles of 8-oxodG and the G4 and explored their interplay at the genomic level.
在核酸的碱基中,鸟嘌呤碱基在暴露于活性氧时,是最容易转化为 8-氧代-7,8-二氢-2'-脱氧鸟苷(8-氧代-dG)的碱基。在双螺旋 DNA 中,8-氧代-dG 可以与腺嘌呤配对;因此,它可能导致 G > T(C > A)突变;它通常被称为一种 DNA 损伤形式,并被 DNA 修复机制及时纠正。此外,8-氧代-dG 最近被重新定义为一种表观遗传因素,影响转录调控元件和其他表观遗传修饰。有人提出,8-氧代-dG 通过与转录调控区域中的非经典 DNA 结构 G-四链体(G4)相互作用来发挥表观遗传控制作用。在这篇综述中,我们重点关注了 8-氧代-dG 和 G4 的表观遗传作用,并探讨了它们在基因组水平上的相互作用。