Evidence map›Paper›PMID 30110627›Full record

ArticleCell reports2018

Attenuated Codon Optimality Contributes to Neural-Specific mRNA Decay in Drosophila.

Dana A Burow, Sophie Martin, Jade F Quail, Najwa Alhusaini, Jeff Coller, Michael D Cleary

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Estimating the evolutionary fitness of specific synonymous codon changes.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Regulation of theRNA (New York, N.Y.) · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. RNA Polymerases I and III in development and disease.Seminars in cell & developmental biology · 2023
    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

6 authors at 2 institutions in 1 country.

Dana A BurowMolecular and Cell Biology Unit, Quantitative and Systems Biology Program, University of California, Merced, Merced, CA 95343, USA.
Sophie MartinCenter for RNA Science and Therapeutics, Case Western Reserve University, Cleveland, OH 44106, USA.
Jade F QuailMolecular and Cell Biology Unit, Quantitative and Systems Biology Program, University of California, Merced, Merced, CA 95343, USA.
Najwa AlhusainiCenter for RNA Science and Therapeutics, Case Western Reserve University, Cleveland, OH 44106, USA.
Jeff CollerCenter for RNA Science and Therapeutics, Case Western Reserve University, Cleveland, OH 44106, USA.
Michael D ClearyMolecular and Cell Biology Unit, Quantitative and Systems Biology Program, University of California, Merced, Merced, CA 95343, USA. Electronic address: mcleary4@ucmerced.edu.
Case Western Reserve University · USUniversity of California, Merced · US

Funding

Understanding the Interconnection Between mRNA turnover and mRNA TranslationR01GM125086 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COLLER, JEFFERY · 2017 to 2020
$1.6M
Determining the influence of codon optimality on mRNA translation and decayR01GM118018 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COLLER, JEFFERY · 2017 to 2020
$1.3M
A Neural Development mRNA Decay NetworkR01HD076927 · NICHD · UNIVERSITY OF CALIFORNIA, MERCED · PI CLEARY, MICHAEL · 2013 to 2017
$1.2M
NICHD NIH HHS R01 HD076927NIGMS NIH HHS R01 GM118018NIGMS NIH HHS R01 GM125086
6 · The paper itself

Abstract

Tissue-specific mRNA stability is important for cell fate and physiology, but the mechanisms involved are not fully understood. We found that zygotic mRNA stability in Drosophila correlates with codon content: optimal codons are enriched in stable transcripts associated with metabolic functions like translation, while non-optimal codons are enriched in unstable transcripts, including those associated with neural development. Bioinformatic analyses and reporter assays revealed that similar codons stabilize or destabilize mRNAs in the nervous system and other tissues, but the link between codon content and stability is attenuated in the nervous system. We confirmed that optimal codons are decoded by abundant tRNAs while non-optimal codons are decoded by less abundant tRNAs in embryos and in the nervous system. We conclude that codon optimality is a general determinant of zygotic mRNA stability, and attenuation of codon optimality allows trans-acting factors to exert greater influence over mRNA decay in the nervous system.

Indexed as

Gene Expression Regulation, DevelopmentalProtein BiosynthesisAnimalsAnimals, Genetically ModifiedCodonComputational BiologyDrosophila melanogasterEmbryo, NonmammalianHalf-LifeHumansNeurogenesisRNA, MessengerRNA StabilityRNA, TransferZygoteCodonRNA, MessengerRNA, Transfercodon optimalitydevelopmentDrosophilamRNA stabilitynervous systemtRNA

Identifiers

PMID30110627
PMCPMC6169788
OpenAlexW2886042183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.