Recognition and catalytic mechanism of tRNA m ³ C methyltransferase METTL6

Post-transcriptional RNA modifications importantly impact RNA structural and functional landscape, and thus play a central role in many cellular processes. Accordingly, aberrant RNA modification pathways underpin a variety of human diseases, including cancer and neurological disorders. However, recognition and catalytic mechanisms of RNA modifying proteins remain obfuscate, due to sparce structural data. Recently, cryogenic electron microscopy structure of m ³ C methyltransferase METTL6 in complex with tRNA ^Ser and seryl-tRNA synthetase (SerRS) was reported. Here, we employ multi-scale computer simulations to ascertain how METTL6, assisted by SerRS, identifies its tRNA ^Ser substrate and catalyzes m ³ C ₃₂ formation. We demonstrate SerRS acts by engaging tRNA ^Ser variable arm to create the interaction surface for METTL6 recruitment. Once METTL6 is appropriately docked at the tRNA ^Ser anticodon stem loop, the methylation reaction proceeds spontaneously. These findings establish the catalytic mechanism of m ³ C RNA methyltransferases and suggest promising avenues for therapeutic targeting.