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Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates

Globin-X (GbX) is an enigmatic member of the vertebrate globin gene family with a wide phyletic distribution that spans protostomes and deuterostomes. Unlike canonical globins such as hemoglobins and myoglobins, functional data suggest that GbX does not have a primary respiratory function. Instead,...

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Autores principales: Hoffmann, Federico G, Storz, Jay F, Kuraku, Shigehiro, Vandewege, Michael W, Opazo, Juan C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525914/
https://www.ncbi.nlm.nih.gov/pubmed/34480557
http://dx.doi.org/10.1093/gbe/evab205
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author Hoffmann, Federico G
Storz, Jay F
Kuraku, Shigehiro
Vandewege, Michael W
Opazo, Juan C
author_facet Hoffmann, Federico G
Storz, Jay F
Kuraku, Shigehiro
Vandewege, Michael W
Opazo, Juan C
author_sort Hoffmann, Federico G
collection PubMed
description Globin-X (GbX) is an enigmatic member of the vertebrate globin gene family with a wide phyletic distribution that spans protostomes and deuterostomes. Unlike canonical globins such as hemoglobins and myoglobins, functional data suggest that GbX does not have a primary respiratory function. Instead, evidence suggests that the monomeric, membrane-bound GbX may play a role in cellular signaling or protection against the oxidation of membrane lipids. Recently released genomes from key vertebrates provide an excellent opportunity to address questions about the early stages of the evolution of GbX in vertebrates. We integrate bioinformatics, synteny, and phylogenetic analyses to characterize the diversity of GbX genes in nonteleost ray-finned fishes, resolve relationships between the GbX genes of cartilaginous fish and bony vertebrates, and demonstrate that the GbX genes of cyclostomes and gnathostomes derive from independent duplications. Our study highlights the role that whole-genome duplications (WGDs) have played in expanding the repertoire of genes in vertebrate genomes. Our results indicate that GbX paralogs have a remarkably high rate of retention following WGDs relative to other globin genes and provide an evolutionary framework for interpreting results of experiments that examine functional properties of GbX and patterns of tissue-specific expression. By identifying GbX paralogs that are products of different WGDs, our results can guide the design of experimental work to explore whether gene duplicates that originate via WGDs have evolved novel functional properties or expression profiles relative to singleton or tandemly duplicated copies of GbX.
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spelling pubmed-85259142021-10-20 Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates Hoffmann, Federico G Storz, Jay F Kuraku, Shigehiro Vandewege, Michael W Opazo, Juan C Genome Biol Evol Research Article Globin-X (GbX) is an enigmatic member of the vertebrate globin gene family with a wide phyletic distribution that spans protostomes and deuterostomes. Unlike canonical globins such as hemoglobins and myoglobins, functional data suggest that GbX does not have a primary respiratory function. Instead, evidence suggests that the monomeric, membrane-bound GbX may play a role in cellular signaling or protection against the oxidation of membrane lipids. Recently released genomes from key vertebrates provide an excellent opportunity to address questions about the early stages of the evolution of GbX in vertebrates. We integrate bioinformatics, synteny, and phylogenetic analyses to characterize the diversity of GbX genes in nonteleost ray-finned fishes, resolve relationships between the GbX genes of cartilaginous fish and bony vertebrates, and demonstrate that the GbX genes of cyclostomes and gnathostomes derive from independent duplications. Our study highlights the role that whole-genome duplications (WGDs) have played in expanding the repertoire of genes in vertebrate genomes. Our results indicate that GbX paralogs have a remarkably high rate of retention following WGDs relative to other globin genes and provide an evolutionary framework for interpreting results of experiments that examine functional properties of GbX and patterns of tissue-specific expression. By identifying GbX paralogs that are products of different WGDs, our results can guide the design of experimental work to explore whether gene duplicates that originate via WGDs have evolved novel functional properties or expression profiles relative to singleton or tandemly duplicated copies of GbX. Oxford University Press 2021-09-04 /pmc/articles/PMC8525914/ /pubmed/34480557 http://dx.doi.org/10.1093/gbe/evab205 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Hoffmann, Federico G
Storz, Jay F
Kuraku, Shigehiro
Vandewege, Michael W
Opazo, Juan C
Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title_full Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title_fullStr Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title_full_unstemmed Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title_short Whole-Genome Duplications and the Diversification of the Globin-X Genes of Vertebrates
title_sort whole-genome duplications and the diversification of the globin-x genes of vertebrates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525914/
https://www.ncbi.nlm.nih.gov/pubmed/34480557
http://dx.doi.org/10.1093/gbe/evab205
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