Evidence map›Paper›PMID 40036501›Full record

ArticleGenetics2025

Season-specific dominance broadly stabilizes polymorphism under symmetric and asymmetric multivoltinism.

Evgeny Brud

Erratum issuedAbstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

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

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Evgeny BrudDepartment of Biological Sciences, North Carolina State University, Raleigh, NC 27607, USA.ORCID 0000-0001-5210-9815

Funding

Genomics of rapid adaptation on seasonal timescales in D. melanogasterR01GM100366 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI SCHMIDT, PAUL · 2012 to 2019
$3.3M
Rapid evolution of pigmentation in D. melanogaster: from cis regulation to phenotypeR01GM137430 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MCINTYRE, LAUREN M., SCHMIDT, PAUL · 2021 to 2024
$2.2M
Computational tools and quantitative analyses of genome structure evolutionR35GM147107 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Rafael F Guerrero · 2022 to 2026
$1.8M
NIGMS NIH HHS R01 GM100366NIGMS NIH HHS R01 GM137430NIGMS NIH HHS R35 GM147107NIGMS NIH HHS R35GM147107NIH HHS R01GM100366
6 · The paper itself

Abstract

Seasonality causes intraannual fitness changes in multivoltine populations (defined as having multiple generations per year). While it is well-known that seasonally balanced polymorphism can be established by overdominance in geometric mean fitness, an unsettled aspect of the deterministic theory is the relative contribution of various season-specific dominance mechanisms to the potential for polymorphism. In particular, the relative importance of seasonal reversals in allelic dominance, where the alleles at a locus alternate in recessivity of their deleterious effects, merits clarification. Here, I analyze the parameter space for the discrete generation two-season multivoltine model and find that biallelic polymorphism is easily maintained owing to an abundance of stabilizing dominance schemes, and moreover, a substantial fraction of these schemes are nonreversing with the season (∼25-50%). In addition, I derive the approximate equilibrium allele frequency cycle under bivoltinism and find that the amplitude of allelic oscillation is maximized by nonreversing dominance if the homozygous fitnesses (per annum) are roughly symmetric. Lastly, I derive conditions for the intralocus evolution of dominance. These predict a long-term trend toward maximally beneficial reversal. Overall, the results counter the disproportionate emphasis placed on dominance reversal as a stabilizing mechanism and clarify that nonreversing dominance is expected to frequently characterize seasonally fluctuating alleles under both weak and strong selection, especially in their early history.

Indexed as

Genes, DominantModels, GeneticPolymorphism, GeneticSeasonsAllelesGene FrequencyGenetic Fitnessantagonistic pleiotropycyclical selectiondominance reversalfluctuating selectiongeometric mean overdominancetemporally varying selection

Identifiers

PMID40036501
PMCPMC12005248

What OpenQuestion holds

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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.