Rocio Diaz Escarcega, Paul Marshall, Andrey S Tsvetkov
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引用次数: 0
摘要
正常细胞在一生中会分裂、受损和修复。随着细胞衰老,它们会进入细胞衰老期,其特征是由各种应激因素引发的细胞周期永久停滞状态。在过去的几十年里,人们一直在积极研究调控衰老表型的分子机制;然而,一个被忽视的领域是 G-四链(G4)DNA 和 RNA(G4-DNA 和 G4-RNA)如何介导衰老。这些非经典的四链 DNA 和 RNA 结构调控着大多数正常的 DNA 和 RNA 依赖过程,如转录、复制和翻译,以及致病机制,包括基因组不稳定性和应激颗粒功能异常。这篇综述还强调了 G4 对年龄相关疾病性别差异的贡献,并强调了通过操纵 G4 针对衰老和抗衰老机制的潜在转化方法。
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.