Evidence map›Paper›PMID 38853722›Full record

ArticleEvolution; international journal of organic evolution2024

Consequences of partially recessive deleterious genetic variation for the evolution of inversions suppressing recombination between sex chromosomes1.

Colin Olito, Suvi Ponnikas, Bengt Hansson, Jessica K Abbott

Abstract readCorrected and Republished Article
In one paragraph

Article in Evolution; international journal of organic evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Sex chromosome evolution in haploid plants: Microchromosomes, disappearing chromosomes, and giant chromosomes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Review
  5. Article
  6. Sex Chromosome Evolution: Hallmarks and Question Marks.Molecular biology and evolution · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Colin OlitoDepartment of Biology, Lund University, Lund, Sweden.ORCID 0000-0001-6883-0367
Suvi PonnikasDepartment of Biology, Lund University, Lund, Sweden.ORCID 0000-0003-3526-2118
Bengt HanssonDepartment of Biology, Lund University, Lund, Sweden.ORCID 0000-0001-6694-8169
Jessica K AbbottDepartment of Biology, Lund University, Lund, Sweden.ORCID 0000-0002-8743-2089

Funding

Olle Engkvist Byggmästare postdoctoral ERC-StG-2015-678148Swedish Research Council Consolidator 2016-00689Wenner-Gren Postdoctoral VR-2022-03603
6 · The paper itself

Abstract

The evolution of suppressed recombination between sex chromosomes is widely hypothesized to be driven by sexually antagonistic selection (SA), where tighter linkage between the sex-determining gene(s) and nearby SA loci is favored when it couples male-beneficial alleles to the proto-Y chromosome, and female-beneficial alleles to the proto-X. Although difficult to test empirically, the SA selection hypothesis overshadows several alternatives, including an incomplete but often-repeated "sheltering" hypothesis which suggests that expansion of the sex-linked region (SLR) reduces the homozygous expression of deleterious mutations at selected loci. Here, we use population genetic models to evaluate the consequences of partially recessive deleterious mutational variation for the evolution of otherwise neutral chromosomal inversions expanding the SLR on proto-Y chromosomes. Both autosomal and SLR-expanding inversions face a race against time: lightly-loaded inversions are initially beneficial, but eventually become deleterious as they accumulate new mutations, after which their chances of fixing become negligible. In contrast, initially unloaded inversions eventually become neutral as their deleterious load reaches the same equilibrium as non-inverted haplotypes. Despite the differences in inheritance and indirect selection, SLR-expanding inversions exhibit similar evolutionary dynamics to autosomal inversions over many biologically plausible parameter conditions. Differences emerge when the population average mutation load is quite high; in this case large autosomal inversions that are lucky enough to be mutation-free can rise to intermediate to high frequencies where selection in homozygotes becomes important (Y-linked inversions never appear as homozygous karyotypes); conditions requiring either high mutation rates, highly recessive deleterious mutations, weak selection, or a combination thereof.

Indexed as

Chromosome InversionEvolution, MolecularRecombination, GeneticAnimalsFemaleGenes, RecessiveGenetic VariationMaleModels, GeneticSelection, GeneticSex Chromosomeschromosomal inversionindirect selectionmutationrecombinationsex chromosomes

Identifiers

PMID38853722
PMCPMC12372689

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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.