Abstract
Epitranscriptomics has emerged as a rapidly evolving field that focused on studying post-transcriptional RNA modifications and their role in spatiotemporal regulation of gene expression. N6-methyladenosine (m6A) and 5-methylcytosine (m5C) represent the most extensively studied modifications on mRNAs. These reversible modifications, mediated by 'writer,' 'eraser,' and 'reader' proteins, dynamically fine-tune mRNA stability, splicing, and translation. Growing evidence links their dysregulation to pathological states, including cancer progression and metastasis, where their aberrant deposition on oncogenes or tumor suppressors alters cellular signaling and therapeutic responses. In the current study, we present a detailed analysis of the m5C epitranscriptomic landscape across distinct breast cancer molecular subtypes. Using CRISPR/Cas9, we confirm NSUN2 as a key m5C writer in human mRNAs. NSUN2 loss was validated by targeted sequencing and Western blotting. Furthermore, we demonstrate the regulatory effects of NSUN2 on its canonical mRNA targets, revealing its critical role in maintaining proper gene expression networks. Our findings strongly suggest that additional m5C writers contribute to m5C methylation machinery. Additionally, we assessed the functional impact of NSUN2 depletion on mRNAs harboring m5C sites using mRNA stability assays. Furthermore, our analysis revealed distinct m5C methylation patterns among breast cancer subtypes, highlighting unique m5C signatures associated with the disease. Notably, we identified specific hypomethylated and hypermethylated m5C sites in each breast cancer cell line, representing a universal m5C methylation signature for breast cancer. Our study constitutes the first comprehensive m5C epitranscriptomic atlas in human breast cancer and paves the way for future research aimed at developing targeted therapeutic interventions that leverage the m5C methylation landscape.