Xu Yirong, Zhang Wei, Shen Feng, Yang Xi, Liu Huilan, Dai Shengbin, Sun Xinchen, Huang Junxing, Guo Qing
Department of Oncology, Taizhou People's Hospital, Taizhou, China.
Graduate school, Dalian Medical University, Dalian, China.
Front Oncol. 2021 Feb 22;11:629560. doi: 10.3389/fonc.2021.629560. eCollection 2021.
-methyladenosine (mA) is the most abundant internal modification in eukaryotic messenger RNAs (mRNAs). mA RNA methylation is involved in all stages of RNA life cycle, from RNA processing, nuclear output, translation regulation to RNA degradation, indicating that mA has various functions affecting RNA metabolism positively or negatively. Reading proteins are vital in regulating the translation and stability of mA mRNAs positively or negatively. Recent studies have enhanced the understanding of the molecular mechanism of the YT521-B homology (YTH) domain family and the modification of mA. This study aimed to review the specific mechanisms, functions, and interactions of the YTH domain protein family. It also discussed future research directions, thus providing new ideas for the clinical diagnosis and targeted therapy of cancer.
N6-甲基腺苷(mA)是真核生物信使核糖核酸(mRNA)中最丰富的内部修饰。mA RNA甲基化参与RNA生命周期的各个阶段,从RNA加工、核输出、翻译调控到RNA降解,这表明mA具有各种对RNA代谢产生正向或负向影响的功能。阅读蛋白在正向或负向调节mA mRNA的翻译和稳定性方面至关重要。最近的研究加深了对YT521-B同源(YTH)结构域家族和mA修饰分子机制的理解。本研究旨在综述YTH结构域蛋白家族的具体机制、功能和相互作用。还讨论了未来的研究方向,从而为癌症的临床诊断和靶向治疗提供新思路。