Evidence map›Paper›PMID 41732107›Full record

ArticleGenetics2026

Overdominance for fitness: a genomic comparison between empirical and simulated data with Drosophila melanogaster.

Inés González-Castellano, Humberto Quesada, Sebastián Ramos-Onsins, Aurora García-Dorado, Armando Caballero

Abstract readComparative Study
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Inés González-CastellanoCentro de Investigación Mariña, Universidade de Vigo, Vigo 36310, Spain.
Humberto QuesadaCentro de Investigación Mariña, Universidade de Vigo, Vigo 36310, Spain.
Sebastián Ramos-OnsinsCentre for Research in Agricultural Genomics CRAG (CSIC-IRTA-UAB-UB), Cerdanyola del Vallès, Barcelona 08193, Spain.ORCID 0000-0002-1776-140X
Aurora García-DoradoDepartamento de Genética, Facultad de Ciencias Biológicas, Universidad Complutense, Madrid 28040, Spain.
Armando CaballeroCentro de Investigación Mariña, Universidade de Vigo, Vigo 36310, Spain.

Funding

Centro singular de investigación de Galicia accreditation 2024-2027 ED431G 2023/07Spanish Ministry of UniversitiesUniversidade de Vigo/CISUGXunta de Galicia ED431C 2024-22
6 · The paper itself

Abstract

Overdominance (heterozygote advantage) for fitness is a form of balancing selection which supports the maintenance of genetic polymorphisms in the populations. This mode of selection is expected to generate a conspicuous footprint on neutral genetic variation in genomic regions of restricted recombination, which contrasts with the signature generated by other types of natural selection. In particular, gene diversity is expected to be increased at neutral sites tightly linked to overdominant sites, as opposed to background selection and selective sweeps. We produced extensive whole-genome sequencing data to analyze genetic diversity across regions exhibiting varying recombination patterns in a Drosophila melanogaster population with known demographic history. The results were compared with simulation data in order to quantify the magnitude of the contribution of overdominant loci to genetic diversity which could be compatible with observations. We analyzed sequencing data from 51 individual male flies sampled from a large population and estimated the average nucleotide diversity (π) in 100-kb consecutive windows across the main autosomal chromosomes. By using the available recombination map in the species, we evaluated the changes in π in relation with the levels of recombination across genomic regions. We then carried out computer simulations following the demographic history, the genomic architecture and the recombination map of the main autosomal chromosomes assuming models which include deleterious (background selection) and advantageous (selective sweeps) mutations, or models also including increasing rates of overdominant mutations. By comparing the results obtained from simulations and the observed data, we conclude that a parsimonious model of background selection and adaptation to captivity explains the observed patterns of neutral variation in the studied population better than the models including overdominance.

Indexed as

Drosophila melanogasterGenetic FitnessSelection, GeneticAnimalsComputer SimulationGenetic VariationGenome, InsectHeterozygoteMaleModels, GeneticRecombination, Geneticbalancing selectioncomputer simulationsheterozygote advantageinbreeding loadnucleotide diversitySNP

Identifiers

PMID41732107
PMCPMC13147538

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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.