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Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles

Chromosomal fusion plays a recurring role in the evolution of adaptations and reproductive isolation among species, yet little is known of the evolutionary drivers of chromosomal fusions. Because sex chromosomes (X and Y in male heterogametic systems, Z and W in female heterogametic systems) differ...

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Autores principales: Pennell, Matthew W., Kirkpatrick, Mark, Otto, Sarah P., Vamosi, Jana C., Peichel, Catherine L., Valenzuela, Nicole, Kitano, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439076/
https://www.ncbi.nlm.nih.gov/pubmed/25993542
http://dx.doi.org/10.1371/journal.pgen.1005237
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author Pennell, Matthew W.
Kirkpatrick, Mark
Otto, Sarah P.
Vamosi, Jana C.
Peichel, Catherine L.
Valenzuela, Nicole
Kitano, Jun
author_facet Pennell, Matthew W.
Kirkpatrick, Mark
Otto, Sarah P.
Vamosi, Jana C.
Peichel, Catherine L.
Valenzuela, Nicole
Kitano, Jun
author_sort Pennell, Matthew W.
collection PubMed
description Chromosomal fusion plays a recurring role in the evolution of adaptations and reproductive isolation among species, yet little is known of the evolutionary drivers of chromosomal fusions. Because sex chromosomes (X and Y in male heterogametic systems, Z and W in female heterogametic systems) differ in their selective, mutational, and demographic environments, those differences provide a unique opportunity to dissect the evolutionary forces that drive chromosomal fusions. We estimate the rate at which fusions between sex chromosomes and autosomes become established across the phylogenies of both fishes and squamate reptiles. Both the incidence among extant species and the establishment rate of Y-autosome fusions is much higher than for X-autosome, Z-autosome, or W-autosome fusions. Using population genetic models, we show that this pattern cannot be reconciled with many standard explanations for the spread of fusions. In particular, direct selection acting on fusions or sexually antagonistic selection cannot, on their own, account for the predominance of Y-autosome fusions. The most plausible explanation for the observed data seems to be (a) that fusions are slightly deleterious, and (b) that the mutation rate is male-biased or the reproductive sex ratio is female-biased. We identify other combinations of evolutionary forces that might in principle account for the data although they appear less likely. Our results shed light on the processes that drive structural changes throughout the genome.
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spelling pubmed-44390762015-05-29 Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles Pennell, Matthew W. Kirkpatrick, Mark Otto, Sarah P. Vamosi, Jana C. Peichel, Catherine L. Valenzuela, Nicole Kitano, Jun PLoS Genet Research Article Chromosomal fusion plays a recurring role in the evolution of adaptations and reproductive isolation among species, yet little is known of the evolutionary drivers of chromosomal fusions. Because sex chromosomes (X and Y in male heterogametic systems, Z and W in female heterogametic systems) differ in their selective, mutational, and demographic environments, those differences provide a unique opportunity to dissect the evolutionary forces that drive chromosomal fusions. We estimate the rate at which fusions between sex chromosomes and autosomes become established across the phylogenies of both fishes and squamate reptiles. Both the incidence among extant species and the establishment rate of Y-autosome fusions is much higher than for X-autosome, Z-autosome, or W-autosome fusions. Using population genetic models, we show that this pattern cannot be reconciled with many standard explanations for the spread of fusions. In particular, direct selection acting on fusions or sexually antagonistic selection cannot, on their own, account for the predominance of Y-autosome fusions. The most plausible explanation for the observed data seems to be (a) that fusions are slightly deleterious, and (b) that the mutation rate is male-biased or the reproductive sex ratio is female-biased. We identify other combinations of evolutionary forces that might in principle account for the data although they appear less likely. Our results shed light on the processes that drive structural changes throughout the genome. Public Library of Science 2015-05-20 /pmc/articles/PMC4439076/ /pubmed/25993542 http://dx.doi.org/10.1371/journal.pgen.1005237 Text en © 2015 Pennell et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pennell, Matthew W.
Kirkpatrick, Mark
Otto, Sarah P.
Vamosi, Jana C.
Peichel, Catherine L.
Valenzuela, Nicole
Kitano, Jun
Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title_full Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title_fullStr Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title_full_unstemmed Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title_short Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles
title_sort y fuse? sex chromosome fusions in fishes and reptiles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439076/
https://www.ncbi.nlm.nih.gov/pubmed/25993542
http://dx.doi.org/10.1371/journal.pgen.1005237
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