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Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
The rateof divergence for Z or X chromosomes is usually observed to be greater than autosomes, but the proposed evolutionary causes for this pattern vary, as do empirical results from diverse taxa. Even among moths and butterflies (Lepidoptera), which generally share a single‐origin Z chromosome, th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291949/ https://www.ncbi.nlm.nih.gov/pubmed/34463346 http://dx.doi.org/10.1111/evo.14341 |
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author | Mongue, Andrew J. Hansen, Megan E. Walters, James R. |
author_facet | Mongue, Andrew J. Hansen, Megan E. Walters, James R. |
author_sort | Mongue, Andrew J. |
collection | PubMed |
description | The rateof divergence for Z or X chromosomes is usually observed to be greater than autosomes, but the proposed evolutionary causes for this pattern vary, as do empirical results from diverse taxa. Even among moths and butterflies (Lepidoptera), which generally share a single‐origin Z chromosome, the handful of available studies give mixed support for faster or more adaptive evolution of the Z chromosome, depending on the species assayed. Here, we examine the molecular evolution of Z chromosomes in two additional lepidopteran species: the Carolina sphinx moth and the monarch butterfly, the latter of which possesses a recent chromosomal fusion yielding a segment of newly Z‐linked DNA. We find evidence for both faster and more adaptive Z chromosome evolution in both species, although this effect is strongest in the neo‐Z portion of the monarch sex chromosome. The neo‐Z is less male‐biased than expected of a Z chromosome, and unbiased and female‐biased genes drive the signal for adaptive evolution here. Together these results suggest that male‐biased gene accumulation and haploid selection have opposing effects on long‐term rates of adaptation and may help explain the discrepancies in previous findings as well as the repeated evolution of neo‐sex chromosomes in Lepidoptera. |
format | Online Article Text |
id | pubmed-9291949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92919492022-07-20 Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*) Mongue, Andrew J. Hansen, Megan E. Walters, James R. Evolution Brief Communications The rateof divergence for Z or X chromosomes is usually observed to be greater than autosomes, but the proposed evolutionary causes for this pattern vary, as do empirical results from diverse taxa. Even among moths and butterflies (Lepidoptera), which generally share a single‐origin Z chromosome, the handful of available studies give mixed support for faster or more adaptive evolution of the Z chromosome, depending on the species assayed. Here, we examine the molecular evolution of Z chromosomes in two additional lepidopteran species: the Carolina sphinx moth and the monarch butterfly, the latter of which possesses a recent chromosomal fusion yielding a segment of newly Z‐linked DNA. We find evidence for both faster and more adaptive Z chromosome evolution in both species, although this effect is strongest in the neo‐Z portion of the monarch sex chromosome. The neo‐Z is less male‐biased than expected of a Z chromosome, and unbiased and female‐biased genes drive the signal for adaptive evolution here. Together these results suggest that male‐biased gene accumulation and haploid selection have opposing effects on long‐term rates of adaptation and may help explain the discrepancies in previous findings as well as the repeated evolution of neo‐sex chromosomes in Lepidoptera. John Wiley and Sons Inc. 2021-09-08 2022-02 /pmc/articles/PMC9291949/ /pubmed/34463346 http://dx.doi.org/10.1111/evo.14341 Text en © 2021 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Communications Mongue, Andrew J. Hansen, Megan E. Walters, James R. Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*) |
title | Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
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title_full | Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
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title_fullStr | Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
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title_full_unstemmed | Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
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title_short | Support for faster and more adaptive Z chromosome evolution in two divergent lepidopteran lineages(*)
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title_sort | support for faster and more adaptive z chromosome evolution in two divergent lepidopteran lineages(*) |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291949/ https://www.ncbi.nlm.nih.gov/pubmed/34463346 http://dx.doi.org/10.1111/evo.14341 |
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