Evidence map›Paper›PMID 29967537›Full record

ArticleNature structural & molecular biology2018

Accurate design of translational output by a neural network model of ribosome distribution.

Robert Tunney, Nicholas J McGlincy, Monica E Graham, Nicki Naddaf, Lior Pachter, Liana F Lareau

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
–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

61 citing papers in PubMed.

  1. Systematic optimization ofEngineering microbiology · 2026
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1 more citing papers are in PubMed but not listed here.

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

6 authors.

Robert TunneyGraduate Group in Computational Biology, University of California, Berkeley, Berkeley, CA, USA.
Nicholas J McGlincyDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0003-1412-2298
Monica E GrahamCalifornia Institute for Quantitative Biosciences, University of California, Berkeley, Berkeley, CA, USA.
Nicki NaddafCalifornia Institute for Quantitative Biosciences, University of California, Berkeley, Berkeley, CA, USA.
Lior PachterDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Liana F LareauCalifornia Institute for Quantitative Biosciences, University of California, Berkeley, Berkeley, CA, USA. lareau@berkeley.edu.ORCID 0000-0003-3223-3426

Funding

PROJECT 3P50GM102706 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI CATE, JAMIE H · 2012 to 2016
$9.5M
Pacific Biosciences PacBio RS Single Molecule Real Time SequencerS10OD018174 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI ROKHSAR, DANIEL SOLEYMAN · 2014 to 2014
$600k
A computational framework for statistical analysis of ribosome profiling dataR21CA202960 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI LAREAU, LIANA FAYE · 2016 to 2017
$366k
NCI NIH HHS R21 CA202960NIGMS NIH HHS P50 GM102706NIH HHS S10 OD018174
6 · The paper itself

Abstract

Synonymous codon choice can have dramatic effects on ribosome speed and protein expression. Ribosome profiling experiments have underscored that ribosomes do not move uniformly along mRNAs. Here, we have modeled this variation in translation elongation by using a feed-forward neural network to predict the ribosome density at each codon as a function of its sequence neighborhood. Our approach revealed sequence features affecting translation elongation and characterized large technical biases in ribosome profiling. We applied our model to design synonymous variants of a fluorescent protein spanning the range of translation speeds predicted with our model. Levels of the fluorescent protein in budding yeast closely tracked the predicted translation speeds across their full range. We therefore demonstrate that our model captures information determining translation dynamics in vivo; that this information can be harnessed to design coding sequences; and that control of translation elongation alone is sufficient to produce large quantitative differences in protein output.

Indexed as

Models, BiologicalProtein BiosynthesisBacterial ProteinsCodonGenes, FungalKineticsLuminescent ProteinsModels, GeneticNeural Networks, ComputerPeptide Chain Elongation, TranslationalRecombinant ProteinsRibosomesRNA, MessengerRNA StabilitySaccharomyces cerevisiaeBacterial Proteinscitrine protein, bacteriaCodonLuminescent ProteinsRecombinant ProteinsRNA, Messenger

Identifiers

PMID29967537
PMCPMC6457438

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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.