Evidence map›Paper›PMID 41761253›Full record

ArticleGenome biology2026

Admixture influences the genetic architecture of DNA methylation in a wild primate hybrid zone.

Tauras P Vilgalys, Jordan A Anderson, Arielle S Fogel, Dana Lin, Elizabeth A Archie, Susan C Alberts, Jenny Tung

Abstract read
In one paragraph

Article in Genome biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tauras P VilgalysDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Jordan A AndersonDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Arielle S FogelDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Dana LinDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Elizabeth A ArchieDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Susan C AlbertsDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Jenny TungDepartment of Evolutionary Anthropology, Duke University, Durham, NC, USA. jtung@eva.mpg.de.

Funding

A life course perspective on gut microbiome aging and health in a non-human primate modelR01AG071684 · NIA · UNIVERSITY OF NOTRE DAME · PI ARCHIE, ELIZABETH · 2021 to 2025
$3.2M
Gene regulation and social relationships across the life course in a nonhuman primate modelR01AG075914 · NIA · DUKE UNIVERSITY · PI ALBERTS, SUSAN C. · 2021 to 2025
$2.6M
Division of Behavioral and Cognitive Sciences BCS-1751783Division of Behavioral and Cognitive Sciences BCS- 2018897Division of Behavioral and Cognitive Sciences BCS-2041621NIH HHS R01AG071684NIH HHS R01AG075914
6 · The paper itself

Abstract

backgroundHybrid zones play a central role in evolutionary biology because they serve as natural laboratories for studying how traits and taxa diverge. Changes in gene regulation make important contributions to this process. However, the degree to which admixture shapes gene regulatory variation in hybrid populations remains poorly understood. Here, we combine genome-wide resequencing and DNA methylation data from 295 hybrid baboons-members of a single, intensively studied natural population-to investigate how admixture affects the genetic architecture of this important epigenetic mark.

resultsWe find that local genetic ancestry frequently predicts DNA methylation levels and recapitulates differences between the parent species. By performing methylation quantitative trait locus mapping, we show that these differences predominantly arise due to evolved differences in allele frequencies. Thus, admixture in the hybrid population increases variance in DNA methylation, including by introducing genetic variants affecting DNA methylation that would otherwise be invariant. Finally, we integrate massively parallel reporter assay data to show that admixture-derived variation in DNA methylation alters enhancer activity and gene expression.

conclusionsTogether, these results demonstrate how admixture can meaningfully alter the genetic architecture of gene regulatory traits in natural hybrid zones. They also suggest that the genetic architecture of DNA methylation is conserved across closely related primates, suggesting that genetic effects on gene regulation may remain stable over timescales that range into the millions of years.

Indexed as

DNA MethylationHybridization, GeneticPapioAnimalsEpigenesis, GeneticGene FrequencyQuantitative Trait LociAdmixtureDNA methylationGene regulationHybridizationMeQTLPapio baboons

Identifiers

PMID41761253
PMCPMC13049888

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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.