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Evolution of stickleback spines through independent cis-regulatory changes at HOXDB
Understanding the mechanisms leading to new traits or additional features in organisms is a fundamental goal of evolutionary biology. We show that HOXDB regulatory changes have been used repeatedly in different fish genera to alter the length and number of the prominent dorsal spines used to classif...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525239/ https://www.ncbi.nlm.nih.gov/pubmed/36050398 http://dx.doi.org/10.1038/s41559-022-01855-3 |
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author | Wucherpfennig, Julia I. Howes, Timothy R. Au, Jessica N. Au, Eric H. Roberts Kingman, Garrett A. Brady, Shannon D. Herbert, Amy L. Reimchen, Thomas E. Bell, Michael A. Lowe, Craig B. Dalziel, Anne C. Kingsley, David M. |
author_facet | Wucherpfennig, Julia I. Howes, Timothy R. Au, Jessica N. Au, Eric H. Roberts Kingman, Garrett A. Brady, Shannon D. Herbert, Amy L. Reimchen, Thomas E. Bell, Michael A. Lowe, Craig B. Dalziel, Anne C. Kingsley, David M. |
author_sort | Wucherpfennig, Julia I. |
collection | PubMed |
description | Understanding the mechanisms leading to new traits or additional features in organisms is a fundamental goal of evolutionary biology. We show that HOXDB regulatory changes have been used repeatedly in different fish genera to alter the length and number of the prominent dorsal spines used to classify stickleback species. In Gasterosteus aculeatus (typically ‘three-spine sticklebacks’), a variant HOXDB allele is genetically linked to shortening an existing spine and adding an additional spine. In Apeltes quadracus (typically ‘four-spine sticklebacks’), a variant HOXDB allele is associated with lengthening a spine and adding an additional spine in natural populations. The variant alleles alter the same non-coding enhancer region in the HOXDB locus but do so by diverse mechanisms, including single-nucleotide polymorphisms, deletions and transposable element insertions. The independent regulatory changes are linked to anterior expansion or contraction of HOXDB expression. We propose that associated changes in spine lengths and numbers are partial identity transformations in a repeating skeletal series that forms major defensive structures in fish. Our findings support the long-standing hypothesis that natural Hox gene variation underlies key patterning changes in wild populations and illustrate how different mutational mechanisms affecting the same region may produce opposite gene expression changes with similar phenotypic outcomes. |
format | Online Article Text |
id | pubmed-9525239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95252392022-10-02 Evolution of stickleback spines through independent cis-regulatory changes at HOXDB Wucherpfennig, Julia I. Howes, Timothy R. Au, Jessica N. Au, Eric H. Roberts Kingman, Garrett A. Brady, Shannon D. Herbert, Amy L. Reimchen, Thomas E. Bell, Michael A. Lowe, Craig B. Dalziel, Anne C. Kingsley, David M. Nat Ecol Evol Article Understanding the mechanisms leading to new traits or additional features in organisms is a fundamental goal of evolutionary biology. We show that HOXDB regulatory changes have been used repeatedly in different fish genera to alter the length and number of the prominent dorsal spines used to classify stickleback species. In Gasterosteus aculeatus (typically ‘three-spine sticklebacks’), a variant HOXDB allele is genetically linked to shortening an existing spine and adding an additional spine. In Apeltes quadracus (typically ‘four-spine sticklebacks’), a variant HOXDB allele is associated with lengthening a spine and adding an additional spine in natural populations. The variant alleles alter the same non-coding enhancer region in the HOXDB locus but do so by diverse mechanisms, including single-nucleotide polymorphisms, deletions and transposable element insertions. The independent regulatory changes are linked to anterior expansion or contraction of HOXDB expression. We propose that associated changes in spine lengths and numbers are partial identity transformations in a repeating skeletal series that forms major defensive structures in fish. Our findings support the long-standing hypothesis that natural Hox gene variation underlies key patterning changes in wild populations and illustrate how different mutational mechanisms affecting the same region may produce opposite gene expression changes with similar phenotypic outcomes. Nature Publishing Group UK 2022-09-01 2022 /pmc/articles/PMC9525239/ /pubmed/36050398 http://dx.doi.org/10.1038/s41559-022-01855-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wucherpfennig, Julia I. Howes, Timothy R. Au, Jessica N. Au, Eric H. Roberts Kingman, Garrett A. Brady, Shannon D. Herbert, Amy L. Reimchen, Thomas E. Bell, Michael A. Lowe, Craig B. Dalziel, Anne C. Kingsley, David M. Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title | Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title_full | Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title_fullStr | Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title_full_unstemmed | Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title_short | Evolution of stickleback spines through independent cis-regulatory changes at HOXDB |
title_sort | evolution of stickleback spines through independent cis-regulatory changes at hoxdb |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525239/ https://www.ncbi.nlm.nih.gov/pubmed/36050398 http://dx.doi.org/10.1038/s41559-022-01855-3 |
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