Li Yang, Ge Yu-Zheng, Xu Luwei, Xu Zheng, Dou Quanliang, Jia Ruipeng
Department of Urology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Front Cell Dev Biol. 2020 Sep 9;8:579919. doi: 10.3389/fcell.2020.579919. eCollection 2020.
N6-methyladenosine (mA) is regarded as the most abundant, prevalent and conserved internal mRNA modification in mammalian cells. MA can be catalyzed by mA methyltransferases METTL3, METTL14 and WTAP (writers), reverted by demethylases ALKBH5 and FTO (erasers), and recognized by mA -binding proteins such as YTHDF1/2/3, IGF2BP1/2/3 and HNRNPA2B1 (readers). Emerging evidence suggests that mA modification is significant for regulating many biological and cellular processes and participates in the pathological development of various diseases, including tumors. This article reviews recent studies on the biological function of mA modification and the methylation modification of mA in urological tumors.
N6-甲基腺苷(mA)被认为是哺乳动物细胞中最丰富、普遍且保守的内部mRNA修饰。mA可由mA甲基转移酶METTL3、METTL14和WTAP(写入器)催化,由去甲基化酶ALKBH5和FTO(擦除器)逆转,并由mA结合蛋白如YTHDF1/2/3、IGF2BP1/2/3和HNRNPA2B1(读取器)识别。新出现的证据表明,mA修饰对于调节许多生物学和细胞过程具有重要意义,并参与包括肿瘤在内的各种疾病的病理发展。本文综述了近年来关于mA修饰的生物学功能以及泌尿肿瘤中mA甲基化修饰的研究。