Evidence map›Paper›PMID 41690953›Full record

ArticleNature communications2026

Actinotrichia-independent developmental mechanisms of spiny rays facilitate the morphological diversification of Acanthomorpha fish fins.

Kazuhide Miyamoto, Junpei Kuroda, Satomi Kamimura, Yasuyuki Sasano, Gembu Abe, Satoshi Ansai, Noriko Funayama, Masahiro Uesaka, Koji Tamura

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Kazuhide MiyamotoDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan. kazuhide.miyamoto.t5@dc.tohoku.ac.jp.ORCID http://orcid.org/0009-0007-6091-6028
Junpei KurodaLaboratory of Organ Morphogenesis, JT Biohistory Research Hall, Osaka, Japan.
Satomi KamimuraDepartment of Environment and Sustainability, School of Environment and Sustainability, Mukogawa Women's University, Nishinomiya, Hyogo, Japan.
Yasuyuki SasanoDivision of Craniofacial Development and Tissue Biology, Graduate School of Dentistry, Tohoku University, Sendai, Miyagi, Japan.
Gembu AbeDivision of Developmental Biology, Department of Functional Morphology, School of Life Science, Faculty of Medicine, Tottori University, Tottori, Japan.ORCID http://orcid.org/0000-0002-9905-8506
Satoshi AnsaiUshimado Marine Institute (UMI), Okayama University, Setouchi, Okayama, Japan.
Noriko FunayamaDepartment of Biophysics, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwake, Sakyo-ku, Kyoto, Japan.
Masahiro UesakaDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan.ORCID http://orcid.org/0000-0002-2927-4860
Koji TamuraDepartment of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan.

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 23KJ0206
6 · The paper itself

Abstract

Skeletal forms in vertebrates have been regarded as good models of morphological diversification. Fish fins show great diversity in form, with their supporting skeletal structure being classified into soft rays and spiny rays. In fish evolution, spiny-ray morphologies are known to be sometimes extremely modified; however, it remains unknown how the developmental mechanisms of spiny rays have contributed to their morphological diversification. By using the rainbowfish Melanotaenia praecox for examination of the extracellular matrix (ECM) and cell dynamics of spiny-ray development, we demonstrate that spiny-ray development is independent of the actinotrichia (needle-shaped collagen polymers at the tip of fins), which are known as an important ECM in soft-ray morphogenesis. Furthermore, we found that in the thorny spiny ray of the filefish Stephanolepis cirrhifer, the lateral protrusions are associated with BMP-positive osteoblast condensation, as in the spiny-ray tips in M. praecox and S. cirrhifer. Taken together, our findings reveal that osteoblast distribution and signaling-molecule intensity would contribute to spiny-ray modification. In comparison to soft ray development, the independence from actinotrichia in spiny rays would facilitate growth direction change, leading to their morphological diversification. This suggests that variation in cell distribution and ECM usage may be important contributors to morphological diversification, not only in Acanthomorpha, but also in other animal taxa.

Indexed as

Animal FinsCollagenFishesAnimalsBiological EvolutionBone Morphogenetic ProteinsExtracellular MatrixMorphogenesisOsteoblastsBone Morphogenetic ProteinsCollagen

Identifiers

PMID41690953
PMCPMC13018208

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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.