Evidence map›Paper›PMID 39008347›Full record

ArticleeLife2024

Enrichment of rare codons at 5' ends of genes is a spandrel caused by evolutionary sequence turnover and does not improve translation.

Richard Sejour, Janet Leatherwood, Alisa Yurovsky, Bruce Futcher

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Ribosome stalling position, spacing, and A-site occupancy impact translation and cotranslational mRNA decay in plants.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Richard SejourDepartment of Pharmacological Sciences, Stony Brook University, Stony Brook, United States.
Janet LeatherwoodDepartment of Microbiology and Immunology, Stony Brook University, Stony Brook, United States.
Alisa YurovskyDepartment of Biomedical Informatics, Stony Brook University, Stony Brook, United States.
Bruce FutcherDepartment of Microbiology and Immunology, Stony Brook University, Stony Brook, United States.ORCID https://orcid.org/0000-0002-1012-9022

Funding

Scaling of transcript abundance with cell size and the commitment to cell divisionR01GM127542 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI BRUCE Bruce FUTCHER · 2019 to 2026
$2.6M
Mechanistic characterization of quantitative trait genetics affecting cell metabolismR01GM132238 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FUTCHER, BRUCE BRUCE, HALEY, JOHN DOUGLAS · 2019 to 2023
$1.4M
NIGMS NIH HHS R01 GM127542NIGMS NIH HHS R01 GM132238NIH HHS RO1 GM127542NIH HHS RO1 GM 132238
6 · The paper itself

Abstract

Previously, Tuller et al. found that the first 30-50 codons of the genes of yeast and other eukaryotes are slightly enriched for rare codons. They argued that this slowed translation, and was adaptive because it queued ribosomes to prevent collisions. Today, the translational speeds of different codons are known, and indeed rare codons are translated slowly. We re-examined this 5' slow translation 'ramp.' We confirm that 5' regions are slightly enriched for rare codons; in addition, they are depleted for downstream Start codons (which are fast), with both effects contributing to slow 5' translation. However, we also find that the 5' (and 3') ends of yeast genes are poorly conserved in evolution, suggesting that they are unstable and turnover relatively rapidly. When a new 5' end forms de novo, it is likely to include codons that would otherwise be rare. Because evolution has had a relatively short time to select against these codons, 5' ends are typically slightly enriched for rare, slow codons. Opposite to the expectation of Tuller et al., we show by direct experiment that genes with slowly translated codons at the 5' end are expressed relatively poorly, and that substituting faster synonymous codons improves expression. Direct experiment shows that slow codons do not prevent downstream ribosome collisions. Further informatic studies suggest that for natural genes, slow 5' ends are correlated with poor gene expression, opposite to the expectation of Tuller et al. Thus, we conclude that slow 5' translation is a 'spandrel'--a non-adaptive consequence of something else, in this case, the turnover of 5' ends in evolution, and it does not improve translation.

Indexed as

CodonEvolution, MolecularProtein BiosynthesisSaccharomyces cerevisiae5' Untranslated RegionsCodon UsageRibosomes5' Untranslated RegionsCodonbiochemistrychemical biologycodon usagecomputational biologyribosome collisionsS. cerevisiaesystems biologytranslationtranslation speed

Identifiers

PMID39008347
PMCPMC11249729

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.