Evidence map›Paper›PMID 40237307›Full record

ArticleeLife2025

The potential of inversions to accumulate balanced sexual antagonism is supported by simulations and

Christopher S McAllester, John E Pool

Abstract read
In one paragraph

Article in eLife, 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. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

  • Update of
    2025
5 · Who and what money

Authors and funding

2 authors.

Christopher S McAllesterLaboratory of Genetics, University of Wisconsin, Madison, United States.ORCID https://orcid.org/0000-0002-4546-1009
John E PoolLaboratory of Genetics, University of Wisconsin, Madison, United States.ORCID https://orcid.org/0000-0003-2968-9545

Funding

Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
The Architectures and Underpinnings of Adaptive Evolution and Reproductive IsolationR35GM136306 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI POOL, JOHN E · 2020 to 2025
$3.5M
National Science Foundation Graduate Research Fellowship Program DGE-1747503NHGRI NIH HHS T32 HG002760NIGMS NIH HHS R35 GM136306NIGMS NIH HHS T32 GM007133
6 · The paper itself

Abstract

Chromosomal inversion polymorphisms can be common, but the causes of their persistence are often unclear. We propose a model for the maintenance of inversion polymorphism, which requires that some variants contribute antagonistically to two phenotypes, one of which has negative frequency-dependent fitness. These conditions yield a form of frequency-dependent disruptive selection, favoring two predominant haplotypes segregating alleles that favor opposing antagonistic phenotypes. An inversion associated with one haplotype can reduce the fitness load incurred by generating recombinant offspring, reinforcing its linkage to the haplotype and enabling both haplotypes to accumulate more antagonistic variants than expected otherwise. We develop and apply a forward simulator to examine these dynamics under a tradeoff between survival and male display. These simulations indeed generate inversion-associated haplotypes with opposing sex-specific fitness effects. Antagonism strengthens with time, and can ultimately yield karyotypes at surprisingly predictable frequencies, with striking genotype frequency differences between sexes and between developmental stages. To test whether this model may contribute to well-studied yet enigmatic inversion polymorphisms in

Indexed as

Chromosome InversionDrosophila melanogasterPolymorphism, GeneticAnimalsComputer SimulationFemaleHaplotypesMaleModels, Geneticbalancing selectionD. melanogasterevolutionary biologyfrequency dependent selectiongeneticsgenomicsinversionpleiotropysexual antagonism

Identifiers

PMID40237307
PMCPMC12002796

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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 OpenQuestion graph.