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Genomics of cold adaptations in the Antarctic notothenioid fish radiation
Numerous novel adaptations characterise the radiation of notothenioids, the dominant fish group in the freezing seas of the Southern Ocean. To improve understanding of the evolution of this iconic fish group, here we generate and analyse new genome assemblies for 24 species covering all major subgro...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256766/ https://www.ncbi.nlm.nih.gov/pubmed/37296119 http://dx.doi.org/10.1038/s41467-023-38567-6 |
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author | Bista, Iliana Wood, Jonathan M. D. Desvignes, Thomas McCarthy, Shane A. Matschiner, Michael Ning, Zemin Tracey, Alan Torrance, James Sims, Ying Chow, William Smith, Michelle Oliver, Karen Haggerty, Leanne Salzburger, Walter Postlethwait, John H. Howe, Kerstin Clark, Melody S. William Detrich, H. Christina Cheng, C.-H. Miska, Eric A. Durbin, Richard |
author_facet | Bista, Iliana Wood, Jonathan M. D. Desvignes, Thomas McCarthy, Shane A. Matschiner, Michael Ning, Zemin Tracey, Alan Torrance, James Sims, Ying Chow, William Smith, Michelle Oliver, Karen Haggerty, Leanne Salzburger, Walter Postlethwait, John H. Howe, Kerstin Clark, Melody S. William Detrich, H. Christina Cheng, C.-H. Miska, Eric A. Durbin, Richard |
author_sort | Bista, Iliana |
collection | PubMed |
description | Numerous novel adaptations characterise the radiation of notothenioids, the dominant fish group in the freezing seas of the Southern Ocean. To improve understanding of the evolution of this iconic fish group, here we generate and analyse new genome assemblies for 24 species covering all major subgroups of the radiation, including five long-read assemblies. We present a new estimate for the onset of the radiation at 10.7 million years ago, based on a time-calibrated phylogeny derived from genome-wide sequence data. We identify a two-fold variation in genome size, driven by expansion of multiple transposable element families, and use the long-read data to reconstruct two evolutionarily important, highly repetitive gene family loci. First, we present the most complete reconstruction to date of the antifreeze glycoprotein gene family, whose emergence enabled survival in sub-zero temperatures, showing the expansion of the antifreeze gene locus from the ancestral to the derived state. Second, we trace the loss of haemoglobin genes in icefishes, the only vertebrates lacking functional haemoglobins, through complete reconstruction of the two haemoglobin gene clusters across notothenioid families. Both the haemoglobin and antifreeze genomic loci are characterised by multiple transposon expansions that may have driven the evolutionary history of these genes. |
format | Online Article Text |
id | pubmed-10256766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102567662023-06-11 Genomics of cold adaptations in the Antarctic notothenioid fish radiation Bista, Iliana Wood, Jonathan M. D. Desvignes, Thomas McCarthy, Shane A. Matschiner, Michael Ning, Zemin Tracey, Alan Torrance, James Sims, Ying Chow, William Smith, Michelle Oliver, Karen Haggerty, Leanne Salzburger, Walter Postlethwait, John H. Howe, Kerstin Clark, Melody S. William Detrich, H. Christina Cheng, C.-H. Miska, Eric A. Durbin, Richard Nat Commun Article Numerous novel adaptations characterise the radiation of notothenioids, the dominant fish group in the freezing seas of the Southern Ocean. To improve understanding of the evolution of this iconic fish group, here we generate and analyse new genome assemblies for 24 species covering all major subgroups of the radiation, including five long-read assemblies. We present a new estimate for the onset of the radiation at 10.7 million years ago, based on a time-calibrated phylogeny derived from genome-wide sequence data. We identify a two-fold variation in genome size, driven by expansion of multiple transposable element families, and use the long-read data to reconstruct two evolutionarily important, highly repetitive gene family loci. First, we present the most complete reconstruction to date of the antifreeze glycoprotein gene family, whose emergence enabled survival in sub-zero temperatures, showing the expansion of the antifreeze gene locus from the ancestral to the derived state. Second, we trace the loss of haemoglobin genes in icefishes, the only vertebrates lacking functional haemoglobins, through complete reconstruction of the two haemoglobin gene clusters across notothenioid families. Both the haemoglobin and antifreeze genomic loci are characterised by multiple transposon expansions that may have driven the evolutionary history of these genes. Nature Publishing Group UK 2023-06-09 /pmc/articles/PMC10256766/ /pubmed/37296119 http://dx.doi.org/10.1038/s41467-023-38567-6 Text en © The Author(s) 2023 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 Bista, Iliana Wood, Jonathan M. D. Desvignes, Thomas McCarthy, Shane A. Matschiner, Michael Ning, Zemin Tracey, Alan Torrance, James Sims, Ying Chow, William Smith, Michelle Oliver, Karen Haggerty, Leanne Salzburger, Walter Postlethwait, John H. Howe, Kerstin Clark, Melody S. William Detrich, H. Christina Cheng, C.-H. Miska, Eric A. Durbin, Richard Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title | Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title_full | Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title_fullStr | Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title_full_unstemmed | Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title_short | Genomics of cold adaptations in the Antarctic notothenioid fish radiation |
title_sort | genomics of cold adaptations in the antarctic notothenioid fish radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256766/ https://www.ncbi.nlm.nih.gov/pubmed/37296119 http://dx.doi.org/10.1038/s41467-023-38567-6 |
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