Evidence map›Paper›PMID 24636000›Full record

ArticleBMC systems biology2014

A condition-specific codon optimization approach for improved heterologous gene expression in Saccharomyces cerevisiae.

Amanda M Lanza, Kathleen A Curran, Lindsey G Rey, Hal S Alper

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 112 citations in OpenAlex.

  1. Review
  2. Article
  3. Metabolic engineering inaBIOTECH · 2025
    Review
  4. Genomic and phenotypic comparison ofbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. EngineeringEngineering microbiology · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Saccharomyces cerevisiae as a Heterologous Host for Natural Products.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  18. Article
  19. CHARMING: Harmonizing synonymous codon usage to replicate a desired codon usage pattern.Protein science : a publication of the Protein Society · 2022
    Article
  20. Article
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.

Amanda M Lanza
Kathleen A Curran
Lindsey G Rey
Hal S AlperDepartment of Chemical Engineering, The University of Texas at Austin, 200 E Dean Keeton St, Stop C0400, Austin, TX 78712, USA. halper@che.utexas.edu.
The University of Texas at Austin · US

Funding

Rerouting Metabolism through Fine-tuned Genetic Control of Essential GenesR01GM090221 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI ALPER, HAL S. · 2009 to 2011
$513k
NIGMS NIH HHS R01GM090221
6 · The paper itself

Abstract

backgroundHeterologous gene expression is an important tool for synthetic biology that enables metabolic engineering and the production of non-natural biologics in a variety of host organisms. The translational efficiency of heterologous genes can often be improved by optimizing synonymous codon usage to better match the host organism. However, traditional approaches for optimization neglect to take into account many factors known to influence synonymous codon distributions.

resultsHere we define an alternative approach for codon optimization that utilizes systems level information and codon context for the condition under which heterologous genes are being expressed. Furthermore, we utilize a probabilistic algorithm to generate multiple variants of a given gene. We demonstrate improved translational efficiency using this condition-specific codon optimization approach with two heterologous genes, the fluorescent protein-encoding eGFP and the catechol 1,2-dioxygenase gene CatA, expressed in S. cerevisiae. For the latter case, optimization for stationary phase production resulted in nearly 2.9-fold improvements over commercial gene optimization algorithms.

conclusionsCodon optimization is now often a standard tool for protein expression, and while a variety of tools and approaches have been developed, they do not guarantee improved performance for all hosts of applications. Here, we suggest an alternative method for condition-specific codon optimization and demonstrate its utility in Saccharomyces cerevisiae as a proof of concept. However, this technique should be applicable to any organism for which gene expression data can be generated and is thus of potential interest for a variety of applications in metabolic and cellular engineering.

Indexed as

Catechol 1,2-DioxygenaseCodonDatabases, GeneticGene ExpressionGreen Fluorescent ProteinsMetabolic EngineeringSaccharomyces cerevisiaeCatechol 1,2-DioxygenaseCodonGreen Fluorescent Proteins

Identifiers

PMID24636000
PMCPMC4004289
OpenAlexW2112689874

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.