Evidence map›Paper›PMID 38722645›Full record

ArticleGenetics2024

Allele frequency dynamics under sex-biased demography and sex-specific inheritance in a pedigreed jay population.

Rose M H Driscoll, Felix E G Beaudry, Elissa J Cosgrove, Reed Bowman, John W Fitzpatrick, Stephan J Schoech, Nancy Chen

Abstract read
In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Rose M H DriscollDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.ORCID 0000-0002-1941-1008
Felix E G BeaudryDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.ORCID 0000-0002-1384-382X
Elissa J CosgroveDepartment of Molecular Biology & Genetics, Cornell University, Ithaca, NY 14850, USA.ORCID 0000-0001-8993-3357
Reed BowmanAvian Ecology Program, Archbold Biological Station, Venus, FL 33960, USA.ORCID 0000-0002-6027-798X
John W FitzpatrickCornell Lab of Ornithology, Cornell University, Ithaca, NY 14850, USA.ORCID 0000-0002-6330-8403
Stephan J SchoechDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152, USA.ORCID 0000-0002-1871-8374
Nancy ChenDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.ORCID 0000-0001-8966-3449

Funding

Population genomics with pedigrees: new approaches for studying contemporary evolutionR35GM133412 · NIGMS · UNIVERSITY OF ROCHESTER · PI CHEN, NANCY · 2019 to 2023
$1.9M
National Science FoundationNIGMS NIH HHS R35 GM133412NIH HHSNSF Graduate Research Fellowship 1939268NSF Postdoctoral Research Fellowship 2109639
6 · The paper itself

Abstract

Sex-biased demography, including sex-biased survival or migration, can alter allele frequency changes across the genome. In particular, we can expect different patterns of genetic variation on autosomes and sex chromosomes due to sex-specific differences in life histories, as well as differences in effective population size, transmission modes, and the strength and mode of selection. Here, we demonstrate the role that sex differences in life history played in shaping short-term evolutionary dynamics across the genome. We used a 25-year pedigree and genomic dataset from a long-studied population of Florida Scrub-Jays (Aphelocoma coerulescens) to directly characterize the relative roles of sex-biased demography and inheritance in shaping genome-wide allele frequency trajectories. We used gene dropping simulations to estimate individual genetic contributions to future generations and to model drift and immigration on the known pedigree. We quantified differential expected genetic contributions of males and females over time, showing the impact of sex-biased dispersal in a monogamous system. Due to female-biased dispersal, more autosomal variation is introduced by female immigrants. However, due to male-biased transmission, more Z variation is introduced by male immigrants. Finally, we partitioned the proportion of variance in allele frequency change through time due to male and female contributions. Overall, most allele frequency change is due to variance in survival and births. Males and females make similar contributions to autosomal allele frequency change, but males make higher contributions to allele frequency change on the Z chromosome. Our work shows the importance of understanding sex-specific demographic processes in characterizing genome-wide allele frequency change in wild populations.

Indexed as

Gene FrequencyPedigreeAnimalsFemaleMaleModels, Geneticpedigreespopulation geneticssex-biased demographysex chromosomes

Identifiers

PMID38722645
PMCPMC11228872

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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.