Arginine methylation of METTL14 promotes RNA N6-methyladenosine modification and endoderm differentiation of mouse embryonic stem cells

作者：Liu, Xiaona; Wang, Hailong; Zhao, Xueya; Luo, Qizhi; Wang, Qingwen; Tan, Kaifen; Wang, Zihan; Jiang, Jia; Cui, Jinru; Du, Enhui; Xia, Linjian; Du, Wenyi; Chen, Dahua^*; Xia, Laixin; Xiao, Shan^*

来源：Nature Communications, 2021, 12(1): 3780.

DOI：10.1038/s41467-021-24035-6

• MESSENGER-RNA
• NUCLEAR-RNA
• METHYLTRANSFERASE 1
• HISTONE H4
• WEB SERVER
• IN-VIVO
• PROTEIN
• REVEALS
• ENZYME
• PRMT1

RNA N-6-methyladenosine (m(6)A), the most abundant internal modification of mRNAs, plays key roles in human development and health. Post-translational methylation of proteins is often critical for the dynamic regulation of enzymatic activity. However, the role of methylation of the core methyltransferase METTL3/METTL14 in m(6)A regulation remains elusive. We find by mass spectrometry that METTL14 arginine 255 (R255) is methylated (R255me). Global mRNA m(6)A levels are greatly decreased in METTL14 R255K mutant mouse embryonic stem cells (mESCs). We further find that R255me greatly enhances the interaction of METTL3/METTL14 with WTAP and promotes the binding of the complex to substrate RNA. We show that protein arginine N-methyltransferases 1 (PRMT1) interacts with and methylates METTL14 at R255, and consistent with this, loss of PRMT1 reduces mRNA m(6)A modification globally. Lastly, we find that loss of R255me preferentially affects endoderm differentiation in mESCs. Collectively, our findings show that arginine methylation of METTL14 stabilizes the binding of the m(6)A methyltransferase complex to its substrate RNA, thereby promoting global m(6)A modification and mESC endoderm differentiation. This work highlights the crosstalk between protein methylation and RNA methylation in gene expression. The methyltransferase complex of METTL3-METTL14-WTAP is responsible for m(6)A modification on RNA. Here the authors report that METTL14 arginine 255 (R255) is methylated by PRMT1 and this modification increases interaction of METTL3/METTL14 interaction with WTAP and substrate RNA, promoting m(6)A methylation activity of the complex.

• 单位
  中国科学院; 广州医学院; 南方医科大学; 云南大学