Evidence map›Paper›PMID 34367575›Full record

ArticleEcology and evolution2021

Demographic history shapes genomic ancestry in hybrid zones.

Megan E Frayer, Bret A Payseur

Abstract read
In one paragraph

Article in Ecology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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

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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Megan E FrayerLaboratory of Genetics University of Wisconsin Madison Madison WI USA.ORCID https://orcid.org/0000-0002-8555-6993
Bret A PayseurLaboratory of Genetics University of Wisconsin Madison Madison WI USA.

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
Evolution of Phenotypic Extremes: Genetic Determinants of Gigantism, Boldness, and RecombinationR35GM139412 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Bret A. Payseur · 2021 to 2026
$5.7M
Evolution of the Genome-wide Recombination Rate in MiceR01GM120051 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PAYSEUR, BRET A · 2017 to 2020
$2.4M
NIGMS NIH HHS R01 GM120051NIGMS NIH HHS R35 GM139412NIGMS NIH HHS T32 GM007133
6 · The paper itself

Abstract

Demographic factors such as migration rate and population size can impede or facilitate speciation. In hybrid zones, reproductive boundaries between species are tested and demography mediates the opportunity for admixture between lineages that are partially isolated. Genomic ancestry is a powerful tool for revealing the history of admixed populations, but models and methods based on local ancestry are rarely applied to structured hybrid zones. To understand the effects of demography on ancestry in hybrids zones, we performed individual-based simulations under a stepping-stone model, treating migration rate, deme size, and hybrid zone age as parameters. We find that the number of ancestry junctions (the transition points between genomic regions with different ancestries) and heterogenicity (the genomic proportion heterozygous for ancestry) are often closely connected to demographic history. Reducing deme size reduces junction number and heterogenicity. Elevating migration rate increases heterogenicity, but migration affects junction number in more complex ways. We highlight the junction frequency spectrum as a novel and informative summary of ancestry that responds to demographic history. A substantial proportion of junctions are expected to fix when migration is limited or deme size is small, changing the shape of the spectrum. Our findings suggest that genomic patterns of ancestry could be used to infer demographic history in hybrid zones.

Indexed as

ancestrygenomicshybrid zonesmigrationspeciation

Identifiers

PMID34367575
PMCPMC8328415

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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.