Evidence map›Paper›PMID 40615540›Full record

ArticleCommunications biology2025

The evolutionary path of the epithelial sodium channel δ-subunit in Cetartiodactyla points to a role in sodium sensing.

Fynn Zahnow, Chiara Jäger, Yassmin Mohamed, Gianluca Vogelhuber, Fabian May, Alexandra Maria Ciocan, Arianna Manieri, Stephan Maxeiner, Gabriela Krasteva-Christ, Oskar Schnappauf and 5 more

Abstract read
In one paragraph

Article in Communications biology, 2025. 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. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Fynn ZahnowInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.ORCID http://orcid.org/0009-0007-0861-2596
Chiara Jäger *Institute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.ORCID http://orcid.org/0009-0000-1045-3861
Yassmin Mohamed *Institute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.
Gianluca Vogelhuber *Institute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.ORCID http://orcid.org/0009-0003-5426-4415
Fabian MayInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.
Alexandra Maria CiocanInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.
Arianna ManieriInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.
Stephan MaxeinerInstitute of Anatomy and Cell Biology, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0002-4472-695X
Gabriela Krasteva-ChristInstitute of Anatomy and Cell Biology, Saarland University, Homburg, Germany.ORCID http://orcid.org/0000-0002-0113-521X
Oskar SchnappaufInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany.ORCID http://orcid.org/0000-0001-8880-3534
Matthew R D CobainDepartment of Biological and Environmental Science, University of Jyväskylä, Jyväskylä, Finland.ORCID http://orcid.org/0000-0003-1701-3986
Lars PodsiadlowskiLeibniz Institute for the Analysis of Biodiversity Change (LIB), Bonn, Germany.ORCID http://orcid.org/0000-0001-7786-8930
José Luis Crespo-PicazoResearch Department, Fundación Oceanogràfic de la Comunitat Valenciana, Valencia, Spain.
Daniel García-PárragaResearch Department, Fundación Oceanogràfic de la Comunitat Valenciana, Valencia, Spain.
Mike AlthausInstitute for Functional Gene Analytics, Bonn-Rhein-Sieg University of Applied Sciences, Rheinbach, Germany. mike.althaus@h-brs.de.ORCID http://orcid.org/0000-0002-3554-7538

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) Project-ID 514177501Deutsche Forschungsgemeinschaft (German Research Foundation) Project-ID 528562393 - FIP 26
6 · The paper itself

Abstract

The epithelial sodium channel (ENaC) is essential for osmoregulation in tetrapod vertebrates. There are four ENaC-subunits (α, β, γ, δ) which form αβγ- or δβγ-ENaCs. While αβγ-ENaC is a 'maintenance protein' controlling sodium homeostasis, δβγ-ENaC might represent a 'stress protein' monitoring high sodium concentrations. The δ-subunit emerged with water-to-land transition of vertebrates. We examined ENaC evolution in Cetartiodactyla, a group including even-toed ungulates and cetaceans (whales, dolphins and porpoises) which returned to marine environments in the Eocene. Genes for α-, β-, and γ-ENaC are intact across Cetartiodactyla. While SCNN1D (δ-ENaC) is intact in terrestrial Artiodactyla, it is a pseudogene in cetaceans. A unique fusion of SCNN1D exons 11 and 12 is observed in the Antilopinae. Transcripts of α-, β-, and γ-ENaC are present in kidney, lung and skin tissues of Bottlenose dolphins, underscoring αβγ-ENaC's maintenance role. Bottlenose dolphins and Beluga whales do not show behavioural differences between sodium-containing and sodium-free stimuli, supporting a function of δ-ENaC as a sodium sensing protein which might have become obsolete in high-salinity marine environments. Consistently, there is reduced selection pressure or pseudogenisation of SCNN1D in other marine mammals. Erosion of SCNN1D might therefore be a consequence of environmental transition in marine mammals.

Indexed as

CetaceaEpithelial Sodium ChannelsEvolution, MolecularSodiumAnimalsPhylogenyEpithelial Sodium ChannelsSodium

Identifiers

PMID40615540
PMCPMC12227717

What OpenQuestion holds

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Registered trials

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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.