Evidence map›Paper›PMID 24710515›Full record

ArticleMolecular biology and evolution2014

Quantifying position-dependent codon usage bias.

Adam J Hockenberry, M Irmak Sirer, Luís A Nunes Amaral, Michael C Jewett

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  4. Macroevolutionary changes in natural selection on codon usage reflect evolution of the tRNA pool across a budding yeast subphylum.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  14. Review
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  17. Integrated analysis of individual codon contribution to protein biosynthesis reveals a new approach to improving the basis of rational gene design.DNA research : an international journal for rapid publication of reports on genes and genomes · 2017
    Article
  18. Article
  19. Article
  20. The Need for Integrated Approaches in Metabolic Engineering.Cold Spring Harbor perspectives in biology · 2016
    Review
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.

Adam J HockenberryDepartment of Chemical and Biological Engineering, Northwestern UniversityInterdepartmental Program in Biological Sciences, Northwestern University.
M Irmak SirerDepartment of Chemical and Biological Engineering, Northwestern University.
Luís A Nunes AmaralDepartment of Chemical and Biological Engineering, Northwestern UniversityNorthwestern Institute on Complex Systems, Northwestern UniversityHoward Hughes Medical Institute, Northwestern University.
Michael C JewettDepartment of Chemical and Biological Engineering, Northwestern UniversityInterdepartmental Program in Biological Sciences, Northwestern UniversityNorthwestern Institute on Complex Systems, Northwestern UniversityChemistry of Life Processes Institute, Northwestern UniversityInstitute for BioNanotechnology and Medicine, Northwestern University m-jewett@northwestern.edu.

Funding

CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
Toward construction of a synthetic self-replicating entityR00GM081450 · NIGMS · NORTHWESTERN UNIVERSITY · PI JEWETT, MICHAEL C · 2009 to 2011
$740k
NIGMS NIH HHS 2-T32GM008061-31NIGMS NIH HHS R00 GM081450NIGMS NIH HHS R00GM081450NIGMS NIH HHS T32 GM008061
6 · The paper itself

Abstract

Although the mapping of codon to amino acid is conserved across nearly all species, the frequency at which synonymous codons are used varies both between organisms and between genes from the same organism. This variation affects diverse cellular processes including protein expression, regulation, and folding. Here, we mathematically model an additional layer of complexity and show that individual codon usage biases follow a position-dependent exponential decay model with unique parameter fits for each codon. We use this methodology to perform an in-depth analysis on codon usage bias in the model organism Escherichia coli. Our methodology shows that lowly and highly expressed genes are more similar in their codon usage patterns in the 5'-gene regions, but that these preferences diverge at distal sites resulting in greater positional dependency (pD, which we mathematically define later) for highly expressed genes. We show that position-dependent codon usage bias is partially explained by the structural requirements of mRNAs that results in increased usage of A/T rich codons shortly after the gene start. However, we also show that the pD of 4- and 6-fold degenerate codons is partially related to the gene copy number of cognate-tRNAs supporting existing hypotheses that posit benefits to a region of slow translation in the beginning of coding sequences. Lastly, we demonstrate that viewing codon usage bias through a position-dependent framework has practical utility by improving accuracy of gene expression prediction when incorporating positional dependencies into the Codon Adaptation Index model.

Indexed as

CodonDNA, BacterialEscherichia coliEscherichia coli ProteinsEvolution, MolecularGenetic VariationLikelihood FunctionsModels, GeneticPhylogenyCodonDNA, BacterialEscherichia coli Proteinscoding sequence evolutioncodon adaptationcodon usage biasgene expression

Identifiers

PMID24710515
PMCPMC4069614

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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.