Evidence map›Paper›PMID 28558053›Full record

ArticlePLoS computational biology2017

Novel mRNA-specific effects of ribosome drop-off on translation rate and polysome profile.

Pierre Bonnin, Norbert Kern, Neil T Young, Ian Stansfield, M Carmen Romano

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 42 citations in OpenAlex.

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  4. A data-driven estimation of the ribosome drop-off rate inNAR genomics and bioinformatics · 2024
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  9. Modelling the effect of ribosome mobility on the rate of protein synthesis.The European physical journal. E, Soft matter · 2021
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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

5 authors at 2 institutions in 2 countries.

Pierre BonninInstitute for Complex Systems and Mathematical Biology, Physics Department, University of Aberdeen, Aberdeen, UK.
Norbert KernUniversité Montpellier 2, Laboratoire Charles Coulomb UMR 5221, Montpellier, France.
Neil T YoungInstitute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, UK.
Ian StansfieldInstitute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, UK.
M Carmen RomanoInstitute for Complex Systems and Mathematical Biology, Physics Department, University of Aberdeen, Aberdeen, UK.ORCID 0000-0002-6261-2147
University of Aberdeen · GBUniversité de Montpellier · FR

Funding

Biotechnology and Biological Sciences Research Council BB/N017161/1
6 · The paper itself

Abstract

The well established phenomenon of ribosome drop-off plays crucial roles in translational accuracy and nutrient starvation responses during protein translation. When cells are under stress conditions, such as amino acid starvation or aminoacyl-tRNA depletion due to a high level of recombinant protein expression, ribosome drop-off can substantially affect the efficiency of protein expression. Here we introduce a mathematical model that describes the effects of ribosome drop-off on the ribosome density along the mRNA and on the concomitant protein synthesis rate. Our results show that ribosome premature termination may lead to non-intuitive ribosome density profiles, such as a ribosome density which increases from the 5' to the 3' end. Importantly, the model predicts that the effects of ribosome drop-off on the translation rate are mRNA-specific, and we quantify their resilience to drop-off, showing that the mRNAs which present ribosome queues are much less affected by ribosome drop-off than those which do not. Moreover, among those mRNAs that do not present ribosome queues, resilience to drop-off correlates positively with the elongation rate, so that sequences using fast codons are expected to be less affected by ribosome drop-off. This result is consistent with a genome-wide analysis of S. cerevisiae, which reveals that under favourable growth conditions mRNAs coding for proteins involved in the translation machinery, known to be highly codon biased and using preferentially fast codons, are highly resilient to ribosome drop-off. Moreover, in physiological conditions, the translation rate of mRNAs coding for regulatory, stress-related proteins, is less resilient to ribosome drop-off. This model therefore allows analysis of variations in the translational efficiency of individual mRNAs by accounting for the full range of known ribosome behaviours, as well as explaining mRNA-specific variations in ribosome density emerging from ribosome profiling studies.

Indexed as

Computational BiologyPolyribosomesProtein BiosynthesisRibosomesRNA, FungalRNA, MessengerSaccharomyces cerevisiaeRNA, FungalRNA, Messenger

Identifiers

PMID28558053
PMCPMC5469512
OpenAlexW2618284730

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.