Comparative analysis of 43 distinct RNA modifications by nanopore tRNA sequencing

• Published in: bioRxiv
• Main Authors: White, Laura K, Dobson, Kezia, Del Pozo, Samantha, Bilodeaux, Jill M, Andersen, Shelby E, Baldwin, Amber, Barrington, Chloe, Körtel, Nadine, Martinez-Seidel, Federico, Strugar, Saylor M, Watt, Kristin E N, Mukherjee, Neelanjan, Hesselberth, Jay R
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory 24.07.2024
• DOI: 10.1101/2024.07.23.604651
• ISSN: 2692-8205

Transfer RNAs are the fundamental adapter molecules of protein synthesis and the most abundant and heterogeneous class of noncoding RNA molecules in cells. The study of tRNA repertoires remains challenging, complicated by the presence of dozens of post transcriptional modifications. Nanopore sequencing is an emerging technology with promise for both tRNA sequencing and the detection of RNA modifications; however, such studies have been limited by the throughput and accuracy of direct RNA sequencing methods. Moreover, detection of the complete set of tRNA modifications by nanopore sequencing remains challenging. Here we show that recent updates to nanopore direct RNA sequencing chemistry (RNA004) combined with our own optimizations to tRNA sequencing protocols and analysis workflows enable high throughput coverage of tRNA molecules and characterization of nanopore signals produced by 43 distinct RNA modifications. We share best practices and protocols for nanopore sequencing of tRNA and further report successful detection of low abundance mitochondrial and viral tRNAs, providing proof of concept for use of nanopore sequencing to study tRNA populations in the context of infection and organelle biology. This work provides a roadmap to guide future efforts towards detection of RNA modifications across multiple organisms using nanopore sequencing.