Diaz Escarcega Rocio, Marshall Paul, Tsvetkov Andrey S
Department of Neurology, University of Texas McGovern Medical School, Houston, TX, United States.
College of Health and Medicine, The Australian National University, Canberra, ACT, Australia.
Front Aging. 2024 Oct 9;5:1491389. doi: 10.3389/fragi.2024.1491389. eCollection 2024.
Normal cells divide, are damaged, and are repaired across their lifetime. As cells age, they enter cellular senescence, characterized by a permanent state of cell-cycle arrest triggered by various stressors. The molecular mechanisms that regulate senescent phenotypes have been actively investigated over the last several decades; however, one area that has been neglected is how G-quadruplex (G4) DNA and RNA (G4-DNA and G4-RNA) mediate senescence. These non-canonical four-stranded DNA and RNA structures regulate most normative DNA and RNA-dependent processes, such as transcription, replication, and translation, as well as pathogenic mechanisms, including genomic instability and abnormal stress granule function. This review also highlights the contribution of G4s to sex differences in age-associated diseases and emphasizes potential translational approaches to target senescence and anti-aging mechanisms through G4 manipulation.
正常细胞在其生命周期中会进行分裂、受损并得到修复。随着细胞衰老,它们会进入细胞衰老状态,其特征是由各种应激源触发的细胞周期永久停滞状态。在过去几十年中,人们一直在积极研究调节衰老表型的分子机制;然而,一个被忽视的领域是G-四链体(G4)DNA和RNA(G4-DNA和G4-RNA)如何介导衰老。这些非规范的四链DNA和RNA结构调节大多数规范的DNA和RNA依赖性过程,如转录、复制和翻译,以及致病机制,包括基因组不稳定和异常应激颗粒功能。本综述还强调了G4对年龄相关疾病中性别差异的贡献,并强调了通过G4操纵来靶向衰老和抗衰老机制的潜在转化方法。