Nanopore direct RNA sequencing reveals METTL2A-mediated m 3 C sites in poly(A) RNA

RNA modifications play critical roles in cellular homeostasis and development by regulating gene expression, RNA metabolism, and translation. Their dysregulation contributes to the development of human diseases, including cancer. 3-methylcytidine (m 3 C) primarily occurs in transfer RNA, where it regulates translation, stem cell pluripotency, and mitochondrial function. m 3 C has also been detected in polyadenylated (poly[A]) RNA by mass spectrometric analysis; however, its transcriptome-wide distribution and functions remain unknown because of its low abundance and technical challenges. Here, we show that METTL2A , an m 3 C writer, is upregulated and associated with poor prognosis in pancreatic cancer tumors, while also being essential for pancreatic cancer cell proliferation. Using comparative nanopore direct RNA sequencing, we identify potential METTL2A-mediated m 3 C sites in poly(A) RNA. These m 3 C sites are mapped in both messenger RNA and mitochondrial RNA and are enriched in the CC motif and coding sequences. METTL2A knockdown alters expression of S100A4 mRNA isoforms, which contains METTL2A-mediated m 3 C sites. Notably, many transcripts with METTL2A-mediated m 3 C sites are upregulated upon METTL2A knockdown. We reveal the transcriptome-wide presence of m 3 C sites in poly(A) RNA and suggest their potential roles in regulating gene expression.