Skip to content
Open access

Linkage disequilibrium moderates how evolving genetic background shapes variant-level architecture

Oct 2026 · bioRxiv · 0 citations · 85 references
Biology

TL;DR

This work develops a model of linkage LD evolution accounting for stabilizing selection, recombination, and genetic drift that deduces the genetic architecture of individual variants subject to the co-evolving genetic background.

Abstract

Evolutionary theory offers a unifying explanation for the genetics of complex traits and diseases by modeling how a trait and its genetic basis are maintained by evolutionary forces. A growing body of evidence suggests that linkage disequilibrium (LD) couples a variant’s evolution to that of the genetic background it resides on. However, widely used single-variant theories omit this coupling between variants and the background, or hold the background fixed. We close this gap by developing a model of linkage LD evolution accounting for stabilizing selection, recombination, and genetic drift. The model deduces the genetic architecture of individual variants subject to the co-evolving genetic background. More efficient selection in larger populations is partially offset by slower decay of existing LD and increased generation of new LD. Conversely, noisier LD in smaller populations exposes the variants to episodes of stronger selection. We ask whether ancestry differences in the relationship between effect-size magnitude and minor allele frequency require different selection strengths or can arise from differences in demographic history alone. Stabilizing selection needs to be more than three times stronger in Africans than in Europeans under the constant-size demography, whereas an Out-of-Africa demography alone can explain most of the observed frequency-dependence gap. As this example indicates, selection strength is in general not identifiable from the frequency–effect-size relationship alone, because different combinations of selection and demographic history can produce the same pattern in data with further redundancy added by LD.

Read PDF

Similar papers

Open access Sep 2026

The effects of supergene evolution on the structure and stability of the G-matrix

It is shown that inversions evolve under disruptive selection and are maintained by balancing selection because they preserve associations among alleles that together generate discrete phenotypic morphs, and stabilise the overall amount of additive genetic variation through time.

Vítor Sudbrack, Charles Mullon · 0 citations
Open access Aug 2026

Consistent and idiosyncratic pleiotropy in shaping genetic correlations

Abstract Pleiotropy, the phenomenon where a single mutation influences multiple phenotypic traits, creates genetic correlations that can constrain evolutionary trajectories. Yet genetic correlations differ in their persistence: some remain stable over long evolutionary timescales, whereas others change rapidly across g...

Haoran Cai, Kerry A. Geiler-Samerotte, D. D. Des Marais · 0 citations
Open access Sep 2026

Evolutionary regimes determine the accuracy of epistasis inference from temporal genetic data.

Epistasis, the non-additive effects of mutations, shapes fitness landscapes and evolutionary trajectories. Temporal genetic data reveal evolutionary dynamics and could be used to infer epistatic interactions, especially through linkage disequilibrium (LD) between interacting mutations. However, other evolutionary force...

Kai S. Shimagaki, John P. Barton · 0 citations
Open access Sep 2026

Recombination accelerates adaptation across genetic architectures and demographic histories

According to classic population genetics theory, recombination shapes the efficacy of natural selection. However, whether variation in recombination rate itself translates into meaningful differences in adaptive capacity remains poorly understood. Here, we used forward-time simulations to examine polygenic adaptation i...

M. Akopyan, Ellie E. Armstrong, K. Samuk · 0 citations
Open access Aug 2026

Sequence architecture shapes human allele frequencies through ectopic gene conversion

It is shown that for a substantial fraction of human variation this assumption fails, and fails predictably: ectopic gene conversion reintroduces the same nucleotide change generation after generation, at rates strongly structured by two fixed properties of genome architecture, homologous template length and donor-acce...

W. Steyaert · 1 citation
Open access Aug 2026

Heritability - A Paradox of Quantitative Genetics.

Heritability is the foundation of quantitative genetics, yet the way it is defined often conflicts with how it is estimated. On one hand, heritability represents the proportion of phenotypic variance explained by genetic variance in the population from which data are sampled. On the other hand, heritability estimated w...

Shi-Zhong Xu · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.