Evidence map›Paper›PMID 42599956›Full record

ArticlePLoS biology2026

A single-cell transcriptomic atlas reveals the emergence of medusa-specific cell states in the scyphozoan Aurelia coerulea.

Oliver Link, Stefan M Jahnel, Kristin Janicek, Daniel Guerguerian, Johanna Kraus, Juan D Montenegro, Bob Zimmermann, Brittney Wick, Konstantin Khalturin, Alison G Cole and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Oliver LinkDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Stefan M JahnelInstitute of Molecular Biotechnology, Vienna, Austria.ORCID https://orcid.org/0000-0003-1147-9179
Kristin JanicekDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Daniel GuerguerianDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Johanna KrausDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Juan D MontenegroDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-4898-5761
Bob ZimmermannDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Brittney WickUCSC Cellbrowser, University of California, Santa Cruz, California, United States of America.
Konstantin KhalturinInstitute of Cellular and Organismic Biology (ICOB), Academia Sinica, Taipei, Taiwan.
Alison G ColeDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-7515-7489
Ulrich TechnauDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-4472-8258

Funding

The UCSC Genome BrowserU24HG002371 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Maximilian Haeussler · 2022 to 2026
$17.6M
A visualization interface for BRAIN single cell data, integrating transcriptomics, epigenomics and spatial assaysRF1MH132662 · NIMH · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI HAEUSSLER, MAXIMILIAN · 2023 to 2023
$866k
NHGRI NIH HHS U24 HG002371NIMH NIH HHS RF1 MH132662
6 · The paper itself

Abstract

The life cycle of most medusozoan cnidarians is marked by the metagenesis from the asexually reproducing sessile polyp and the sexually reproducing motile medusa. At present, it is unknown to what extent this drastic morphological transformation is accompanied by molecular changes in the cell type composition. Here, we provide a single-cell transcriptome atlas of the cosmopolitan scyphozoan Aurelia coerulea focusing on changes in individual cell states during the transition from polyp to medusa. Notably, this transition is marked by an increase in cell type diversity, including an expansion of neural subtypes and the appearance of striated muscles. We find that two families of neuronal lineages are specified by homologous transcription factors in the sea anemone Nematostella vectensis and A. coerulea, suggesting an origin in the common ancestor of medusozoans and anthozoans about 500 Myr ago. Our analysis suggests that gene duplications might be drivers for the increase of cellular complexity during the evolution of cnidarian neuroglandular lineages and highlights the close relationship of neurons and muscles. One key medusozoan-specific cell type is the striated muscle in the subumbrella. Evaluating muscle types by fiber anatomy and gene expression validation of their individual molecular profiles made it possible for the first time to investigate transcriptome differences between smooth and striated muscles. Although smooth and striated muscles are phenotypically different, both have a similar regulation of the contractile complex, reminiscent to the regulation of smooth muscles in bilaterians. This contrasts with bilaterian striated muscles, where the regulation of muscle contraction involves Ca2+ binding troponins and their interaction with Tropomyosin. These data suggest that smooth muscle contraction regulation is ancestral and the use of troponins in striated muscles only evolved in bilaterians.

Indexed as

CnidariaTranscriptomeAnimalsNeuronsPhylogenySea AnemonesSingle-Cell AnalysisSingle-Cell Gene Expression Analysis

Identifiers

PMID42599956
PMCPMC13485128

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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.