Evidence map›Paper›PMID 40853969›Full record

ArticlePLoS biology2025

Caudal fin shape imprinted during late zebrafish embryogenesis is re-patterned by the Sonic hedgehog pathway.

Eric Surette, Joan Donahue, Crisvely Soto Martinez, Stephanie Robinson, Deirdre McKenna, Brendan Fitzgerald, Katherine Backus, Rolf O Karlstrom, Nicolás Cumplido, Sarah K McMenamin

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Early ultraviolet exposure disrupts late dorsal fin skeletal development in zebrafish.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Eric SuretteBoston College, Chestnut Hill, Massachusetts, United States of America.
Joan DonahueBoston College, Chestnut Hill, Massachusetts, United States of America.
Crisvely Soto MartinezBoston College, Chestnut Hill, Massachusetts, United States of America.
Stephanie RobinsonBoston College, Chestnut Hill, Massachusetts, United States of America.
Deirdre McKennaBoston College, Chestnut Hill, Massachusetts, United States of America.
Brendan FitzgeraldBoston College, Chestnut Hill, Massachusetts, United States of America.
Katherine BackusBoston College, Chestnut Hill, Massachusetts, United States of America.
Rolf O KarlstromUniversity of Massachusetts, Amherst, Massachusetts, United States of America.
Nicolás CumplidoBoston College, Chestnut Hill, Massachusetts, United States of America.
Sarah K McMenaminBoston College, Chestnut Hill, Massachusetts, United States of America.ORCID 0000-0002-1154-5810

Funding

Illuminating the mechanisms that generate pattern and shape during growth and regeneration of the zebrafish finR35GM146467 · NIGMS · BOSTON COLLEGE · PI Sarah Kelly McMenamin · 2022 to 2026
$1.9M
NIGMS NIH HHS R35 GM146467
6 · The paper itself

Abstract

Appendage shape is formed during development-and re-established during regeneration-according to spatial and temporal cues that orchestrate local cell behaviors. The caudal fin is the primary appendage used for propulsion in most fishes, and the organ exhibits a range of distinct morphologies adapted for different swimming strategies. The external caudal fin of the zebrafish develops with a forked shape, with longer supportive bony rays at the periphery and shorter rays at the center of the organ. Here, we show that inducing a transient pulse of sonic hedgehog a (shha) overexpression during late embryonic development leads to excess growth of the central rays, causing the adult caudal fin to grow into a triangular, truncate shape. Our results identify a period-prior to endogenous shha expression and before differentiation of skeletogenic cells in these tissues-during which the imprinted fin shape can be re-patterned by hyper-physiological Shh stimulation. After this critical developmental period, overexpression of shha does not alter the shape of the adult caudal fin. Both global and local shha overexpression during the critical window of embryogenesis are sufficient to alter the fin shape, and a normal forked shape can be rescued by subsequent treatment with an antagonist of the canonical Shh pathway. The early pulse of shha expands hox13 expression domains in the fin primordium, and leads to excessive proliferation in the central regions of the fin. After developing with a truncate shape, a truncate morphology was remembered and rebuilt during regeneration, suggesting that the shape imprinted during embryogenesis informs both developmental and regenerative morphogenesis. Ray-finned fishes have evolved a wide spectrum of caudal morphologies, and the current work offers insights into the developmental time periods and processes that inform growth and ultimate shape of the fin.

Indexed as

Animal FinsBody PatterningHedgehog ProteinsZebrafishZebrafish ProteinsAnimalsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalSignal TransductionHedgehog ProteinsShha protein, zebrafishZebrafish Proteins

Identifiers

PMID40853969
PMCPMC12396763

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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.