Structural insights into the recognition and catalysis of tRNA by human NSUN2

Abstract The human RNA m 5 C methyltransferase NSUN2 catalyzes site-specific cytosine methylation across diverse RNA substrates and thereby regulates a wide range of biological and physiological processes. However, the molecular basis by which NSUN2 achieves broad substrate recognition while maintaining catalytic specificity has remained unclear. Here we determine structures of human NSUN2 in both substrate-free and substrate-bound states using X-ray crystallography and cryo-electron microscopy. Structures of NSUN2 in complex with multiple tRNA substrates reveal a structure-first, sequence-tolerant strategy in which NSUN2 actively remodels tRNA architecture, exposing the buried target cytosine and positioning it within the catalytic pocket for methyl transfer. This recognition strategy enables NSUN2 to accommodate diverse tRNA substrates through a largely conserved interaction interface. Guided by these structural insights, we identify a small-molecule inhibitor that suppresses NSUN2 activity and cancer cell proliferation. Together, our findings define the molecular principles underlying NSUN2-mediated RNA m 5 C modification and provide a structural foundation for targeting NSUN2 in cancers.