bioRxivBiophysicsPreprint
Combinations of slow translating codon clusters can increase mRNA half-life
Abstract
The introduction of a single, non-optimal codon cluster into a transcript was found to cause ribosomes to queue upstream of it and decrease the transcripts half-life through the action of the dead box protein Dhh1p, which interacts with stalled ribosomes and promotes transcript degradation. Naturally occurring transcripts often contain multiple slow codon clusters, but the influence of these combinations of clusters on a transcripts half-life is unknown. Using a kinetic model that describes translation and mRNA degradation, we find that the introduction of a second slow codon cluster into a transcript near the 5'-end can have the opposite effect than that of the first cluster by increasing the mRNAs half-life. We experimentally validate this finding by showing that S. cerevisiae transcripts that only have a slow codon cluster towards the 3'-end of the coding sequence have shorter half-lives than transcripts with non-optimal clusters at both 3' and 5' -ends. The origin of this increase in half-life arises from the 5'-end cluster suppressing the formation of ribosome queues upstream of the second cluster, thereby decreasing the opportunities for translation-dependent degradation machinery, such as the Dhh1p protein, to interact with stalled ribosomes. We also find in the model that in the presence of two slow codon clusters the cluster closest to 5'-end is the primary determinant of mRNA half-life. These results identify two of the rules governing the influence of slow codon clusters on mRNA half-life, demonstrate that multiple slow codon clusters can have synergistic effects, and indicate that codon usage bias can play a more nuanced role in controlling cellular protein levels than previously thought.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Factors regulating translation coupled mRNA degradation in yeast
Sudipto Basu, Raktim Maiti, … Sudip Kundu·bioRxiv·Apr 1, 2022
- Massively parallel identification of sequence motifs triggering ribosome-associated mRNA quality control
Katharine Y. Chen, Heungwon Park, Arvind Rasi Subramaniam·Nucleic Acids ResearchPeer-reviewed·Apr 4, 2024
- Rif-seq reveals Caulobacter crescentus mRNA decay is globally coordinated with transcription and translation
Hiranthi Kulathungage, James R. Aretakis, … Jared M. Schrader·bioRxiv·Apr 22, 2025
- Redistribution of codon-optimality effects: measurement strategy alters the division of labor between translation and mRNA decay
Sayanur Rahaman, Samuel Mondal, … Attila Becskei·bioRxiv·May 23, 2026
- Non-invasive measurement of mRNA decay reveals translation initiation as the major determinant of mRNA stability
Leon Y Chan, Christopher Frederick Mugler, … Karsten Weis·eLifePeer-reviewed·Sep 7, 2018
- Codon stabilization coefficient as an index for prediction of codon bias and its potential applications.
Rodolfo Lopes Carneiro, Rodrigo Dias Requião, … Fernando Lucas Palhano·Nucleic Acids ResearchPeer-reviewed·Jan 14, 2019