Evidence map›Paper›PMID 40966227›Full record

ArticlePLoS genetics2025

Single-cell consequences of X-linked meiotic drive in stalk-eyed flies.

Peter D Price, Sylvie M Parkus, Victoria J Lloyd, Ben T Alston, Sasha L Bradshaw, Sadé Bates, Margaret A Hughes, Steve Paterson, Terry Burke, Iulia Darolti and 2 more

Abstract read
In one paragraph

Article in PLoS genetics, 2025. 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. 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

12 authors.

Peter D PriceEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0000-0002-6118-1111
Sylvie M ParkusEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Victoria J LloydEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0009-0006-8467-0133
Ben T AlstonEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Sasha L BradshawDepartment of Genetics, Evolution and Environment, University College London, London, United Kingdom.
Sadé BatesDepartment of Genetics, Evolution and Environment, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-9736-1077
Margaret A HughesCentre for Genomic Research, University of Liverpool, Liverpool, United Kingdom.
Steve PatersonCentre for Genomic Research, University of Liverpool, Liverpool, United Kingdom.
Terry BurkeEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.
Iulia DaroltiDepartment of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-5865-4969
Andrew PomiankowskiDepartment of Genetics, Evolution and Environment, University College London, London, United Kingdom.
Alison E WrightEcology and Evolutionary Biology, School of Biosciences, University of Sheffield, Sheffield, United Kingdom.ORCID https://orcid.org/0000-0003-2479-5250

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sex-linked meiotic drivers limit the inheritance of the alternate sex chromosome in the heterogametic sex, subsequently skewing the offspring sex ratio. They consequently have large impacts on genome evolution, adaptation, and the emergence and maintenance of sexually selected traits. Despite this, our understanding of their molecular basis and consequences for gametogenesis and sex chromosome regulation more broadly has focused on a handful of model organisms, primarily Drosophila and mouse, which are not representative of the broad diversity of reproductive modes and drive systems in nature. Here, we employ single-cell RNA sequencing (scRNA-seq) to investigate a sex-linked meiotic driver in the Malaysian stalk-eyed fly, Teleopsis dalmanni. First, we produce a comprehensive single-cell atlas of the male T. dalmanni gonad and identify major testis cell types. We then provide a comprehensive profile of the cellular and transcriptional landscape of the testis, providing evidence for a lack of complete meiotic sex chromosome inactivation and complex trajectory of dosage compensation. Second, by contrasting single-cell expression data between drive and standard testes, we provide insight into the consequences of a meiotic driver for the transcriptomic landscape of the testis and sex chromosome regulation. Importantly, we show that the presence of a meiotic driver does not perturb fundamental patterns of X-linked regulation. Our results provide insight into how the meiotic driver might bias its transmission to the next generation and highlight genes with perturbed expression as a potential consequence of the disruption of spermatogenesis.

Indexed as

DipteraMeiosisAnimalsDosage Compensation, GeneticFemaleGenes, X-LinkedMaleSex ChromosomesSingle-Cell AnalysisTestisTranscriptomeX ChromosomeX Chromosome Inactivation

Identifiers

PMID40966227
PMCPMC12445520

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.