Cancer mutations rewire the RNA methylation specificity of METTL3-METTL14.

Chemical modification of RNAs is important for post-transcriptional gene regulation. The METTL3-METTL14 complex generates most -methyladenosine (m A) modifications in mRNAs, and dysregulated methyltransferase expression has been linked to numerous cancers. Here we show that changes in m A modification location can impact oncogenesis. A gain-of-function missense mutation found in cancer patients, METTL14 , promotes malignant cell growth in culture and in transgenic mice. The mutant methyltransferase preferentially modifies noncanonical sites containing a GGAU motif and transforms gene expression without increasing global m A levels in mRNAs. The altered substrate specificity is intrinsic to METTL3-METTL14, helping us to propose a structural model for how the METTL3-METTL14 complex selects the cognate RNA sequences for modification. Together, our work highlights that sequence-specific m A deposition is important for proper function of the modification and that noncanonical methylation events can impact aberrant gene expression and oncogenesis.