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Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes

In the white-throated sparrow (Zonotrichia albicollis), the second chromosome bears a striking resemblance to sex chromosomes. First, within each breeding pair of birds, one bird is homozygous for the standard arrangement of the chromosome (ZAL2/ZAL2) and its mate is heterozygous for a different ver...

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Autores principales: Sun, Dan, Huh, Iksoo, Zinzow-Kramer, Wendy M., Maney, Donna L., Yi, Soojin V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856536/
https://www.ncbi.nlm.nih.gov/pubmed/29483264
http://dx.doi.org/10.1073/pnas.1717721115
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author Sun, Dan
Huh, Iksoo
Zinzow-Kramer, Wendy M.
Maney, Donna L.
Yi, Soojin V.
author_facet Sun, Dan
Huh, Iksoo
Zinzow-Kramer, Wendy M.
Maney, Donna L.
Yi, Soojin V.
author_sort Sun, Dan
collection PubMed
description In the white-throated sparrow (Zonotrichia albicollis), the second chromosome bears a striking resemblance to sex chromosomes. First, within each breeding pair of birds, one bird is homozygous for the standard arrangement of the chromosome (ZAL2/ZAL2) and its mate is heterozygous for a different version (ZAL2/ZAL2(m)). Second, recombination is profoundly suppressed between the two versions, leading to genetic differentiation between them. Third, the ZAL2(m) version is linked with phenotypic traits, such as bright plumage, high aggression, and low parental behavior, which are usually associated with males. These similarities to sex chromosomes suggest that the evolutionary mechanisms that shape sex chromosomes, in particular genetic degeneration of the heterogametic version due to the suppression of recombination, are likely important in this system as well. Here, we investigated patterns of protein sequence evolution and gene expression evolution between the ZAL2 and ZAL2(m) chromosomes by whole-genome sequencing and transcriptome analyses. Patterns of protein evolution exhibited only weak signals of genetic degeneration, and few genes harbored signatures of positive selection. We found substantial evidence of transcriptome evolution, such as significant expression divergence between ZAL2 and ZAL2(m) alleles and signatures of dosage compensation for highly expressed genes. These results suggest that, early in the evolution of heteromorphic chromosomes, gene expression divergence and dosage compensation can prevail before large-scale genetic degeneration. Our results show further that suppression of recombination between heteromorphic chromosomes can lead to the evolution of alternative (sex-like) behavioral phenotypes before substantial genetic degeneration.
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spelling pubmed-58565362018-04-05 Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes Sun, Dan Huh, Iksoo Zinzow-Kramer, Wendy M. Maney, Donna L. Yi, Soojin V. Proc Natl Acad Sci U S A Biological Sciences In the white-throated sparrow (Zonotrichia albicollis), the second chromosome bears a striking resemblance to sex chromosomes. First, within each breeding pair of birds, one bird is homozygous for the standard arrangement of the chromosome (ZAL2/ZAL2) and its mate is heterozygous for a different version (ZAL2/ZAL2(m)). Second, recombination is profoundly suppressed between the two versions, leading to genetic differentiation between them. Third, the ZAL2(m) version is linked with phenotypic traits, such as bright plumage, high aggression, and low parental behavior, which are usually associated with males. These similarities to sex chromosomes suggest that the evolutionary mechanisms that shape sex chromosomes, in particular genetic degeneration of the heterogametic version due to the suppression of recombination, are likely important in this system as well. Here, we investigated patterns of protein sequence evolution and gene expression evolution between the ZAL2 and ZAL2(m) chromosomes by whole-genome sequencing and transcriptome analyses. Patterns of protein evolution exhibited only weak signals of genetic degeneration, and few genes harbored signatures of positive selection. We found substantial evidence of transcriptome evolution, such as significant expression divergence between ZAL2 and ZAL2(m) alleles and signatures of dosage compensation for highly expressed genes. These results suggest that, early in the evolution of heteromorphic chromosomes, gene expression divergence and dosage compensation can prevail before large-scale genetic degeneration. Our results show further that suppression of recombination between heteromorphic chromosomes can lead to the evolution of alternative (sex-like) behavioral phenotypes before substantial genetic degeneration. National Academy of Sciences 2018-03-13 2018-02-26 /pmc/articles/PMC5856536/ /pubmed/29483264 http://dx.doi.org/10.1073/pnas.1717721115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Sun, Dan
Huh, Iksoo
Zinzow-Kramer, Wendy M.
Maney, Donna L.
Yi, Soojin V.
Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title_full Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title_fullStr Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title_full_unstemmed Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title_short Rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
title_sort rapid regulatory evolution of a nonrecombining autosome linked to divergent behavioral phenotypes
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856536/
https://www.ncbi.nlm.nih.gov/pubmed/29483264
http://dx.doi.org/10.1073/pnas.1717721115
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