m6A in the coding sequence: linking deposition, translation, and decay

N6-methyladenosine (m6A) is the most abundant internal modification in mRNA and plays a crucial role in regulating mRNA turnover. This review explores the characteristics of m6A sites in the coding sequence (CDS) and their influence on mRNA decay, with a focus on the newly discovered CDS–m6A decay (CMD) pathway – a translation-dependent mechanism that promotes rapid and efficient degradation. Further, we examine how splicing-associated factors influence m6A deposition and discuss the enrichment of CMD targets in processing bodies (P-bodies). We emphasize the interplay between m6A modification and decay, and propose that targeting the CMD pathway could offer novel therapeutic strategies for diseases such as cancer and metabolic disorders.