Evidence map›Paper›PMID 41252186›Full record

ArticleeLife2025

Removal of developmentally regulated microexons has a minimal impact on larval zebrafish brain morphology and function.

Caleb C S Calhoun, Mary E S Capps, Kristie Muya, William C Gannaway, Verdion Martina, Claire L Conklin, Morgan C Klein, Jhodi M Webster, Emma G Torija-Olson, Summer B Thyme

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

10 authors.

Caleb C S CalhounDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Mary E S CappsDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Kristie MuyaDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
William C GannawayDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Verdion MartinaDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Claire L ConklinDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Morgan C KleinDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Jhodi M WebsterDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.
Emma G Torija-OlsonDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.ORCID https://orcid.org/0000-0001-5003-7395
Summer B ThymeDepartment of Neurobiology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, United States.ORCID https://orcid.org/0000-0003-3593-4148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microexon splicing is a vertebrate-conserved process through which small, often in-frame, exons are differentially included during brain development and across neuron types. Although the protein sequences encoded by these exons are highly conserved and can mediate interactions, the neurobiological functions of only a small number have been characterized. To establish a more generalized understanding of their roles in brain development, we used CRISPR/Cas9 to remove 45 microexons in zebrafish and assessed larval brain activity, morphology, and behavior. Most mutants had minimal or no phenotypes at this developmental stage. Among previously studied microexons, we uncovered baseline and stimulus-driven phenotypes for two microexons (meA and meB) in

Indexed as

Alternative SplicingBrainExonsGene Expression Regulation, DevelopmentalZebrafishZebrafish ProteinsAnimalsCRISPR-Cas SystemsLarvaPhenotypeZebrafish Proteinsalternative splicingCRISPR/Cas9developmental biologymicroexonneurosciencezebrafish

Identifiers

PMID41252186
PMCPMC12626420

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.