Near-cognate tRNAs dominate codon decoding times in simulated ribosomes
The codon sequence of messenger RNAs affects ribosome dynamics, translational control, and transcript stability. Here, we describe an advanced computational modelling tool and its application to studying the effect of different tRNA species on the codon decoding process. Using tRNA abundance data for Saccharomyce cerevisiae, we show that simulated codon decoding times are sensitive to the abundance of near- and non-cognate tRNAs as well as cognate species. Codon decoding times predicted by models that accurately define near-cognate tRNAs and that are parameterized with high-quality tRNA abundance datasets are highly similar to ribosome dwell times determined using experimental ribosome footprinting data, thereby confirming both the importance of near-cognate tRNAs for the codon decoding process and the general accuracy of our modelling tools.
Authors
- C. Mark Smales (ORCID: https://orcid.org/0000-0002-2762-4724)
- Anne E. Willis (ORCID: https://orcid.org/0000-0002-1470-8531)
- James Thaventhiran (ORCID: https://orcid.org/0000-0001-8616-074X)
- Tobias von der Haar (ORCID: https://orcid.org/0000-0002-6031-9254)
- Emma Hargreaves (ORCID: https://orcid.org/0000-0002-7091-919X)
- Sathishkumar Kurusamy (ORCID: https://orcid.org/0000-0003-2608-9827)
- Fábio de Lima Hedayioglu (ORCID: https://orcid.org/0000-0003-0609-0054)
Institutions
- MRC Laboratory of Molecular Biology (GB)
- University of Kent (GB)
- Bridge University (SS)
- Io Therapeutics (United States) (US)
- National Institute for Bioprocessing Research and Training (IE)
Publication Details
- Journal
- Nucleic Acids Research
- Published
- 2025-10-28
- DOI
- https://doi.org/10.1093/nar/gkaf1164
- Primary Topic
- RNA and protein synthesis mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Wellcome Trust
- Directorate for Biological Sciences
- Medical Research Council