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Population Genetics of Reproductive Genes in Haplodiploid Species

Many animal species are haplodiploid: their fertilized eggs develop into diploid females and their unfertilized eggs develop into haploid males. The unique genetic features of haplodiploidy raise the prospect that these systems can be used to disentangle the population genetic consequences of haploi...

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Autores principales: Dapper, Amy L., Slater, Garett P., Shores, Katherynne, Harpur, Brock A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156000/
https://www.ncbi.nlm.nih.gov/pubmed/35640985
http://dx.doi.org/10.1093/gbe/evac070
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author Dapper, Amy L.
Slater, Garett P.
Shores, Katherynne
Harpur, Brock A.
author_facet Dapper, Amy L.
Slater, Garett P.
Shores, Katherynne
Harpur, Brock A.
author_sort Dapper, Amy L.
collection PubMed
description Many animal species are haplodiploid: their fertilized eggs develop into diploid females and their unfertilized eggs develop into haploid males. The unique genetic features of haplodiploidy raise the prospect that these systems can be used to disentangle the population genetic consequences of haploid and diploid selection. To this end, sex-specific reproductive genes are of particular interest because, while they are shared within the same genome, they consistently experience selection in different ploidal environments. However, other features of these genes, including sex-specific expression and putative involvement in postcopulatory sexual selection, are potentially confounding factors because they may also impact the efficacy of selection asymmetrically between the sexes. Thus, to properly interpret evolutionary genomic patterns, it is necessary to generate a null expectation for the relative amount of polymorphism and divergence we expect to observe among sex-specific genes in haplodiploid species, given differences in ploidal environment, sex-limited expression, and their potential role in sexual selection. Here, we derive the theoretical expectation for the rate of evolution of sex-specific genes in haplodiploid species, under the assumption that they experience the same selective environment as genes expressed in both sexes. We find that the null expectation is that reproductive genes evolve more rapidly than constitutively expressed genes in haplodiploid genomes. However, despite the aforementioned differences, the null expectation does not differ between male- and female-specific reproductive genes, when assuming additivity. Our theoretical results provide an important baseline expectation that should be used in molecular evolution studies comparing rates of evolution among classes of genes in haplodiploid species.
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spelling pubmed-91560002022-06-04 Population Genetics of Reproductive Genes in Haplodiploid Species Dapper, Amy L. Slater, Garett P. Shores, Katherynne Harpur, Brock A. Genome Biol Evol Letter Many animal species are haplodiploid: their fertilized eggs develop into diploid females and their unfertilized eggs develop into haploid males. The unique genetic features of haplodiploidy raise the prospect that these systems can be used to disentangle the population genetic consequences of haploid and diploid selection. To this end, sex-specific reproductive genes are of particular interest because, while they are shared within the same genome, they consistently experience selection in different ploidal environments. However, other features of these genes, including sex-specific expression and putative involvement in postcopulatory sexual selection, are potentially confounding factors because they may also impact the efficacy of selection asymmetrically between the sexes. Thus, to properly interpret evolutionary genomic patterns, it is necessary to generate a null expectation for the relative amount of polymorphism and divergence we expect to observe among sex-specific genes in haplodiploid species, given differences in ploidal environment, sex-limited expression, and their potential role in sexual selection. Here, we derive the theoretical expectation for the rate of evolution of sex-specific genes in haplodiploid species, under the assumption that they experience the same selective environment as genes expressed in both sexes. We find that the null expectation is that reproductive genes evolve more rapidly than constitutively expressed genes in haplodiploid genomes. However, despite the aforementioned differences, the null expectation does not differ between male- and female-specific reproductive genes, when assuming additivity. Our theoretical results provide an important baseline expectation that should be used in molecular evolution studies comparing rates of evolution among classes of genes in haplodiploid species. Oxford University Press 2022-05-12 /pmc/articles/PMC9156000/ /pubmed/35640985 http://dx.doi.org/10.1093/gbe/evac070 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Letter
Dapper, Amy L.
Slater, Garett P.
Shores, Katherynne
Harpur, Brock A.
Population Genetics of Reproductive Genes in Haplodiploid Species
title Population Genetics of Reproductive Genes in Haplodiploid Species
title_full Population Genetics of Reproductive Genes in Haplodiploid Species
title_fullStr Population Genetics of Reproductive Genes in Haplodiploid Species
title_full_unstemmed Population Genetics of Reproductive Genes in Haplodiploid Species
title_short Population Genetics of Reproductive Genes in Haplodiploid Species
title_sort population genetics of reproductive genes in haplodiploid species
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156000/
https://www.ncbi.nlm.nih.gov/pubmed/35640985
http://dx.doi.org/10.1093/gbe/evac070
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