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Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes

How consistent are the evolutionary trajectories of sex chromosomes shortly after they form? Insights into the evolution of recombination, differentiation, and degeneration can be provided by comparing closely related species with homologous sex chromosomes. The sex chromosomes of the threespine sti...

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Autores principales: Sardell, Jason M, Josephson, Matthew P, Dalziel, Anne C, Peichel, Catherine L, Kirkpatrick, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476171/
https://www.ncbi.nlm.nih.gov/pubmed/34117766
http://dx.doi.org/10.1093/molbev/msab179
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author Sardell, Jason M
Josephson, Matthew P
Dalziel, Anne C
Peichel, Catherine L
Kirkpatrick, Mark
author_facet Sardell, Jason M
Josephson, Matthew P
Dalziel, Anne C
Peichel, Catherine L
Kirkpatrick, Mark
author_sort Sardell, Jason M
collection PubMed
description How consistent are the evolutionary trajectories of sex chromosomes shortly after they form? Insights into the evolution of recombination, differentiation, and degeneration can be provided by comparing closely related species with homologous sex chromosomes. The sex chromosomes of the threespine stickleback (Gasterosteus aculeatus) and its sister species, the Japan Sea stickleback (G. nipponicus), have been well characterized. Little is known, however, about the sex chromosomes of their congener, the blackspotted stickleback (G. wheatlandi). We used pedigrees to obtain experimentally phased whole genome sequences from blackspotted stickleback X and Y chromosomes. Using multispecies gene trees and analysis of shared duplications, we demonstrate that Chromosome 19 is the ancestral sex chromosome and that its oldest stratum evolved in the common ancestor of the genus. After the blackspotted lineage diverged, its sex chromosomes experienced independent and more extensive recombination suppression, greater X–Y differentiation, and a much higher rate of Y degeneration than the other two species. These patterns may result from a smaller effective population size in the blackspotted stickleback. A recent fusion between the ancestral blackspotted stickleback Y chromosome and Chromosome 12, which produced a neo-X and neo-Y, may have been favored by the very small size of the recombining region on the ancestral sex chromosome. We identify six strata on the ancestral and neo-sex chromosomes where recombination between the X and Y ceased at different times. These results confirm that sex chromosomes can evolve large differences within and between species over short evolutionary timescales.
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spelling pubmed-84761712021-09-28 Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes Sardell, Jason M Josephson, Matthew P Dalziel, Anne C Peichel, Catherine L Kirkpatrick, Mark Mol Biol Evol Discoveries How consistent are the evolutionary trajectories of sex chromosomes shortly after they form? Insights into the evolution of recombination, differentiation, and degeneration can be provided by comparing closely related species with homologous sex chromosomes. The sex chromosomes of the threespine stickleback (Gasterosteus aculeatus) and its sister species, the Japan Sea stickleback (G. nipponicus), have been well characterized. Little is known, however, about the sex chromosomes of their congener, the blackspotted stickleback (G. wheatlandi). We used pedigrees to obtain experimentally phased whole genome sequences from blackspotted stickleback X and Y chromosomes. Using multispecies gene trees and analysis of shared duplications, we demonstrate that Chromosome 19 is the ancestral sex chromosome and that its oldest stratum evolved in the common ancestor of the genus. After the blackspotted lineage diverged, its sex chromosomes experienced independent and more extensive recombination suppression, greater X–Y differentiation, and a much higher rate of Y degeneration than the other two species. These patterns may result from a smaller effective population size in the blackspotted stickleback. A recent fusion between the ancestral blackspotted stickleback Y chromosome and Chromosome 12, which produced a neo-X and neo-Y, may have been favored by the very small size of the recombining region on the ancestral sex chromosome. We identify six strata on the ancestral and neo-sex chromosomes where recombination between the X and Y ceased at different times. These results confirm that sex chromosomes can evolve large differences within and between species over short evolutionary timescales. Oxford University Press 2021-06-12 /pmc/articles/PMC8476171/ /pubmed/34117766 http://dx.doi.org/10.1093/molbev/msab179 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Discoveries
Sardell, Jason M
Josephson, Matthew P
Dalziel, Anne C
Peichel, Catherine L
Kirkpatrick, Mark
Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title_full Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title_fullStr Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title_full_unstemmed Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title_short Heterogeneous Histories of Recombination Suppression on Stickleback Sex Chromosomes
title_sort heterogeneous histories of recombination suppression on stickleback sex chromosomes
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476171/
https://www.ncbi.nlm.nih.gov/pubmed/34117766
http://dx.doi.org/10.1093/molbev/msab179
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