Selective profiling of translationally active tRNAs and their dynamics under stress

During translation, transfer RNAs (tRNAs) deliver specific amino acids to the ribosome in a coordinated manner with the sequence encoded by the messenger RNA. Despite their central role in protein synthesis, their precise contribution to the modulation of translation remains poorly understood, primarily due to lack of methods to characterize tRNA abundances and their modifications from actively translating ribosomes. Here we develop tRIBO-seq, a simple and robust nanopore-based method to selectively capture ribosome-associated native tRNA populations (ribo-tRNAs) from actively translating ribosomes, providing tRNA abundance, modification and fragmentation information from a single experiment. Using tRIBO-seq, we find that ribo-tRNAs, but often not total tRNAs, are significantly altered on stress. Notably, we find that tRNAome alterations strongly vary depending on the stress type; while viral infection and leucine deprivation leads to changes in ribo-tRNA abundances, methionine starvation causes a dramatic loss of methyl-based tRNA modifications. By contrast, we find that arsenite exposure does not alter tRNA abundances nor modification patterns, but rather causes major fragmentation events in selected subsets of ribo-tRNAs. Altogether, tRIBO-seq offers a robust and reproducible approach to map the full tRNA landscape-capturing tRNA abundance, modification and fragmentation patterns-across both total and actively translating tRNA populations, revealing the dynamics of the tRNAome with unprecedented resolution, in a single experiment.

Authors

Institutions

Publication Details

Journal
Nature Methods
Published
2026-11-02
DOI
https://doi.org/10.1038/s41592-026-03277-6
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
1.72
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Selective profiling of translationally active tRNAs and their dynamics under stress

Ana Raquel Soares, Michele Arnoldi, Massimiliano Clamer, Isabelle Bonomo et al.
1 citations
Nature Methods
RNA and protein synthesis mechanisms
1.72
article

Selective profiling of translationally active tRNAs and their dynamics under stress

Ana Raquel Soares, Michele Arnoldi, Massimiliano Clamer, Isabelle Bonomo, Daniela Ribeiro, Laia Llovera, Eva Maria Novoa, Alessia Del Piano, Mie Monti, Jéssica Sarabando, Hasan Yilmaz
article en
1 citations

Abstract

During translation, transfer RNAs (tRNAs) deliver specific amino acids to the ribosome in a coordinated manner with the sequence encoded by the messenger RNA. Despite their central role in protein synthesis, their precise contribution to the modulation of translation remains poorly understood, primarily due to lack of methods to characterize tRNA abundances and their modifications from actively translating ribosomes. Here we develop tRIBO-seq, a simple and robust nanopore-based method to selectively capture ribosome-associated native tRNA populations (ribo-tRNAs) from actively translating ribosomes, providing tRNA abundance, modification and fragmentation information from a single experiment. Using tRIBO-seq, we find that ribo-tRNAs, but often not total tRNAs, are significantly altered on stress. Notably, we find that tRNAome alterations strongly vary depending on the stress type; while viral infection and leucine deprivation leads to changes in ribo-tRNA abundances, methionine starvation causes a dramatic loss of methyl-based tRNA modifications. By contrast, we find that arsenite exposure does not alter tRNA abundances nor modification patterns, but rather causes major fragmentation events in selected subsets of ribo-tRNAs. Altogether, tRIBO-seq offers a robust and reproducible approach to map the full tRNA landscape-capturing tRNA abundance, modification and fragmentation patterns-across both total and actively translating tRNA populations, revealing the dynamics of the tRNAome with unprecedented resolution, in a single experiment.

Nature Methods
Institució Catalana de Recerca i Estudis Avançats (ES), Universitat Pompeu Fabra (ES), Barcelona Institute of Science and Technology (ES), Centre for Genomic Regulation (ES), University of Aveiro (PT)
Openalex Percentile: Top 20%
RNA and protein synthesis mechanisms
1.72
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon