Evidence map›Paper›PMID 41481677›Full record

ArticlePloS one2026

B chromosome retrotransposed sequences persist through speciation, contributing to genomic and regulatory innovations in the fish genus Psalidodon (Characiformes, Acestrorhamphidae).

Lucas F Lasmar, Mateus R Vidal, Pamela C F Nadai, Rodrigo Zeni Dos Santos, Raquel da Costa Machado, Ricardo Utsunomia, Francisco J Ruiz-Ruano, Alexander Suh, Claudio Oliveira, Duilio M Z A Silva and 1 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. B chromosomes put the 'super' in supernumerary.Trends in genetics : TIG · 2026
    Review
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.

Lucas F LasmarDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.
Mateus R VidalDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-1532-5452
Pamela C F NadaiDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.ORCID https://orcid.org/0009-0005-8627-8584
Rodrigo Zeni Dos SantosDepartamento de Ciências Biológicas, Faculdade de Ciências, Universidade Estadual Paulista, UNESP, Campus de Bauru, Bauru, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-3034-255X
Raquel da Costa MachadoDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.
Ricardo UtsunomiaDepartamento de Ciências Biológicas, Faculdade de Ciências, Universidade Estadual Paulista, UNESP, Campus de Bauru, Bauru, São Paulo, Brazil.
Francisco J Ruiz-RuanoCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Bonn, North Rhine-Westphalia, Germany.
Alexander SuhCentre for Molecular Biodiversity Research, Leibniz Institute for the Analysis of Biodiversity Change, Bonn, North Rhine-Westphalia, Germany.
Claudio OliveiraDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.
Duilio M Z A SilvaDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-2610-2254
Fausto ForestiDepartamento de Biologia Estrutural e Funcional, Instituto de Biociências de Botucatu, Universidade Estadual Paulista, UNESP, Botucatu, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B chromosomes are supernumerary genetic elements rich in repetitive DNA. Many species within the fish genus Psalidodon possess a large metacentric B chromosome that exhibits signs of recent retrotransposon activity, resulting in truncated pseudogenic copies of standard A chromosomes genes, specifically sbno2 and simc1. We aimed to characterize the structure of the B chromosome pseudogenes sbno2-B and simc1-B and their evolutionary history in four B chromosome variants of three Psalidodon species, as well as their expression patterns in Psalidodon paranae individuals with a single B chromosome (1B). Our findings suggest that the retrotransposition process of each gene occurred in an ancestral B chromosome, which later diverged into distinct trajectories within each species following speciation. In the high-copy B chromosomes, the sbno2-B pseudogene shows dozens of interspersed copies, while the simc1-B pseudogene usually shows three copies arranged in tandem. In Psalidodon paranae 1B individuals, underexpression of the sbno2 and simc1 genes in ovaries indicates that the pseudogenic B copies probably influence gene expression through non-coding RNA interference mechanisms. This shows that the retrotransposon activity on B chromosomes generates genomic diversity and neofunctionalization, impacting gene regulatory networks, and possibly contributing to the persistence of B chromosome in populations.

Indexed as

CharaciformesChromosomesGenetic SpeciationRetroelementsAnimalsEvolution, MolecularFemaleGenomePhylogenyPseudogenesRetroelements

Identifiers

PMID41481677
PMCPMC12758807

What OpenQuestion holds

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LicenceCC BY
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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.