Suboptimal codon pairs trigger ribosome collisions and cellular quality control responses in tRNA modification mutants

Transfer RNA (tRNA) modifications tune translation rates and codon optimality, thereby optimizing co-translational protein folding. However, the mechanisms by which tRNA modifications modulate codon optimality and trigger phenotypes remain unclear. Here, we show that ribosomes stall at specific modification-dependent codon pairs in wobble uridine modification (U34) mutants. This triggers ribosome collisions and a coordinated hierarchical response of cellular quality control pathways. High-resolution ribosome profiling reveals an unexpected functional diversity of U34 modifications during decoding. For instance, 5-carbamoylmethyluridine (ncm5U) exhibits distinct effects at the A and P sites. Importantly, ribosomes only slow down at a fraction of codons decoded by hypomodified tRNA, and the decoding speed of most codons remains unaffected. However, the translation speed of a codon largely depends on the identity of A- and P-site codons. Stalling at modification-dependent codon pairs induces ribosome collisions, triggering ribosome-associated quality control (RQC) and preventing protein aggregation by degrading aberrant nascent peptides and messenger RNAs. Inactivation of RQC stimulates the expression of molecular chaperones that remove protein aggregates. Our results demonstrate that loss of tRNA modifications primarily disrupts translation rates of suboptimal codon pairs, showing the coordinated regulation and adaptability of cellular surveillance systems. These systems ensure efficient and accurate protein synthesis and maintain protein homeostasis.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-11-05
DOI
https://doi.org/10.1093/nar/gkaf1311
Citations
3
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
2.42

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article

Suboptimal codon pairs trigger ribosome collisions and cellular quality control responses in tRNA modification mutants

Olga Sin, Sebastian Glatt, Claudine Kraft, Héctor Mancilla et al.
3 citations
Nucleic Acids Research
RNA modifications and cancer
2.42
article

Suboptimal codon pairs trigger ribosome collisions and cellular quality control responses in tRNA modification mutants

Olga Sin, Sebastian Glatt, Claudine Kraft, Héctor Mancilla, Jan M. Bruder, Tristan Ranff, Sebastian A. Leidel, Christian Fufezan, Fabienne Mollet, Cristián Eggers, Hans R Schöler, Jie Wu, Hannes C A Drexler, Łukasz Koziej
article en
3 citations

Abstract

Transfer RNA (tRNA) modifications tune translation rates and codon optimality, thereby optimizing co-translational protein folding. However, the mechanisms by which tRNA modifications modulate codon optimality and trigger phenotypes remain unclear. Here, we show that ribosomes stall at specific modification-dependent codon pairs in wobble uridine modification (U34) mutants. This triggers ribosome collisions and a coordinated hierarchical response of cellular quality control pathways. High-resolution ribosome profiling reveals an unexpected functional diversity of U34 modifications during decoding. For instance, 5-carbamoylmethyluridine (ncm5U) exhibits distinct effects at the A and P sites. Importantly, ribosomes only slow down at a fraction of codons decoded by hypomodified tRNA, and the decoding speed of most codons remains unaffected. However, the translation speed of a codon largely depends on the identity of A- and P-site codons. Stalling at modification-dependent codon pairs induces ribosome collisions, triggering ribosome-associated quality control (RQC) and preventing protein aggregation by degrading aberrant nascent peptides and messenger RNAs. Inactivation of RQC stimulates the expression of molecular chaperones that remove protein aggregates. Our results demonstrate that loss of tRNA modifications primarily disrupts translation rates of suboptimal codon pairs, showing the coordinated regulation and adaptability of cellular surveillance systems. These systems ensure efficient and accurate protein synthesis and maintain protein homeostasis.

Nucleic Acids ResearchVol. 53(22)
University of Bern (CH), Jagiellonian University (PL), Bern University of Applied Sciences (CH), University of Veterinary Medicine Vienna (AT), University of Freiburg (DE), Heidelberg University (DE), Max Planck Institute for Molecular Biomedicine (DE), Heidelberg University (US)
National Science Foundation, European Commission, Deutsche Forschungsgemeinschaft, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 10%
RNA modifications and cancer
2.42
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