Evidence map›Paper›PMID 28598992›Full record

ArticlePLoS computational biology2017

Ribosome reinitiation can explain length-dependent translation of messenger RNA.

David W Rogers, Marvin A Böttcher, Arne Traulsen, Duncan Greig

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

25 citing papers in PubMed, 43 citations in OpenAlex.

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  6. An algorithmic constraint at the transition to complex life.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  10. A Chimeric ORF Fusion Phenotypic Reporter forJournal of fungi (Basel, Switzerland) · 2024
    Article
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  12. Length-Dependent Translation Efficiency of ER-Destined Proteins.Current issues in molecular biology · 2023
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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 at 1 institution in 2 countries.

David W RogersExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.ORCID http://orcid.org/0000-0002-1431-2676
Marvin A BöttcherDepartment of Evolutionary Theory, Max Planck Institute for Evolutionary Biology, Plön, Germany.ORCID http://orcid.org/0000-0003-3992-5273
Arne TraulsenDepartment of Evolutionary Theory, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Duncan GreigExperimental Evolution Research Group, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Max Planck Institute for Evolutionary Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Models of mRNA translation usually presume that transcripts are linear; upon reaching the end of a transcript each terminating ribosome returns to the cytoplasmic pool before initiating anew on a different transcript. A consequence of linear models is that faster translation of a given mRNA is unlikely to generate more of the encoded protein, particularly at low ribosome availability. Recent evidence indicates that eukaryotic mRNAs are circularized, potentially allowing terminating ribosomes to preferentially reinitiate on the same transcript. Here we model the effect of ribosome reinitiation on translation and show that, at high levels of reinitiation, protein synthesis rates are dominated by the time required to translate a given transcript. Our model provides a simple mechanistic explanation for many previously enigmatic features of eukaryotic translation, including the negative correlation of both ribosome densities and protein abundance on transcript length, the importance of codon usage in determining protein synthesis rates, and the negative correlation between transcript length and both codon adaptation and 5' mRNA folding energies. In contrast to linear models where translation is largely limited by initiation rates, our model reveals that all three stages of translation-initiation, elongation, and termination/reinitiation-determine protein synthesis rates even at low ribosome availability.

Indexed as

Computer SimulationModels, ChemicalModels, GeneticPeptide Chain Elongation, TranslationalPeptide Chain Initiation, TranslationalProtein Modification, TranslationalRibosomesRNA, MessengerStructure-Activity RelationshipTranscription FactorsRNA, MessengerTranscription Factors

Identifiers

PMID28598992
PMCPMC5482490
OpenAlexW2949309588

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.