Evidence map›Paper›PMID 27542830›Full record

ArticleGenes & development2016

Codon usage affects the structure and function of the Drosophila circadian clock protein PERIOD.

Jingjing Fu, Katherine A Murphy, Mian Zhou, Ying H Li, Vu H Lam, Christine A Tabuloc, Joanna C Chiu, Yi Liu

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 2 pooled it
–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

48 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. eLife · 2026
    Article
  7. Article
  8. Estimating the evolutionary fitness of specific synonymous codon changes.bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Article
  11. Circadian rhythms: pervasive, and often times evasive.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  12. Translation Rates and Protein Folding.Journal of molecular biology · 2024
    Review
  13. Article
  14. Review
  15. Mammalian circadian clock proteins form dynamic interacting microbodies distinct from phase separation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

8 authors at 2 institutions in 2 countries.

Jingjing FuDepartment of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;
Katherine A MurphyDepartment of Entomology and Nematology, University of California at Davis, Davis, California 95616, USA;
Mian ZhouDepartment of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA; School of Biotechnology, East China University of Science and Technology, Shanghai 200237, China.
Ying H LiDepartment of Entomology and Nematology, University of California at Davis, Davis, California 95616, USA;
Vu H LamDepartment of Entomology and Nematology, University of California at Davis, Davis, California 95616, USA;
Christine A TabulocDepartment of Entomology and Nematology, University of California at Davis, Davis, California 95616, USA;
Joanna C ChiuDepartment of Entomology and Nematology, University of California at Davis, Davis, California 95616, USA;
Yi LiuDepartment of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;
University of California, Davis · USThe University of Texas Southwestern Medical Center · US

Funding

Mechanisms of Circadian Clock and Gene Sliencing in NeurosporaR35GM118118 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI LIU, YI · 2016 to 2025
$6.3M
The role of DBT and NEMO-dependent phosphoproteome in regulating animal clockworkR01GM102225 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIU, JOANNA CHUNGYEN · 2013 to 2017
$1.4M
NIGMS NIH HHS R01 GM102225NIGMS NIH HHS R35 GM118118
6 · The paper itself

Abstract

Codon usage bias is a universal feature of all genomes, but its in vivo biological functions in animal systems are not clear. To investigate the in vivo role of codon usage in animals, we took advantage of the sensitivity and robustness of the Drosophila circadian system. By codon-optimizing parts of Drosophila period (dper), a core clock gene that encodes a critical component of the circadian oscillator, we showed that dper codon usage is important for circadian clock function. Codon optimization of dper resulted in conformational changes of the dPER protein, altered dPER phosphorylation profile and stability, and impaired dPER function in the circadian negative feedback loop, which manifests into changes in molecular rhythmicity and abnormal circadian behavioral output. This study provides an in vivo example that demonstrates the role of codon usage in determining protein structure and function in an animal system. These results suggest a universal mechanism in eukaryotes that uses a codon usage "code" within genetic codons to regulate cotranslational protein folding.

Indexed as

AnimalsCircadian RhythmCodonDrosophilaDrosophila ProteinsFeedback, PhysiologicalPeriod Circadian ProteinsPhosphorylationProtein FoldingProtein StabilityProtein Structure, TertiaryCodonDrosophila ProteinsPeriod Circadian ProteinsPER protein, Drosophilacircadian clockcodon usageDrosophilaperiodprotein structure

Identifiers

PMID27542830
PMCPMC5002980
OpenAlexW2516990920

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.