Nanopore direct RNA sequencing of human transcriptomes reveals the complexity of mRNA modifications and crosstalk between regulatory features

作者：Yerin Kim, Luke Saville, Kieran O’Neill, Jean‐Michel Garant, Yilin Liu, Simon Haile-Merhu, Maryam Ghashghaei, Quang Anh Hoang, Amber Louwagie, Yongjin Park, Steven J.M. Jones, Ly Vu · 发表于：Cell Genomics · 年份：2025 · DOI：10.1016/j.xgen.2025.100872 · 被引用次数：22 · 研究领域：RNA modifications and cancer、RNA Research and Splicing、RNA and protein synthesis mechanisms

The identification and functional characterization of chemical modifications on an mRNA molecule, in particular N 6 -methyladenosine (m 6 A) modification, significantly broadened our understanding of RNA function and regulation. While interactions between RNA modifications and other RNA features have been proposed, direct evidence showing correlation is limited. Here, using Oxford Nanopore long-read direct RNA sequencing (dRNA-seq), we simultaneously interrogate the transcriptome and epitranscriptome of a human leukemia cell line to investigate the correlation between m 6 A modifications, mRNA abundance, mRNA stability, polyadenylation (poly(A)) tail length, and alternative splicing. High-quality dRNA-seq is important for unbiased and large-scale correlative analyses. Global assessments indicated a negative association between poly(A) tail length and mRNA abundance while uncovering pathway-specific responses upon depletion of the m 6 A-forming enzyme METTL3. Overall, our study presented a rich dRNA-seq data resource that has been validated and can be further exploited to inquire into the complexity of RNA modifications and potential interplays between RNA regulatory elements.