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Evolution of the Growth Hormone Gene Duplication in Passerine Birds

Birds of the order Passeriformes represent the most speciose order of land vertebrates. Despite strong scientific interest in this super-radiation, genetic traits unique to passerines are not well characterized. A duplicate copy of growth hormone (GH) is the only gene known to be present in all majo...

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Autores principales: Rasband, Shauna A, Bolton, Peri E, Fang, Qi, Johnson, Philip L F, Braun, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016047/
https://www.ncbi.nlm.nih.gov/pubmed/36848146
http://dx.doi.org/10.1093/gbe/evad033
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author Rasband, Shauna A
Bolton, Peri E
Fang, Qi
Johnson, Philip L F
Braun, Michael J
author_facet Rasband, Shauna A
Bolton, Peri E
Fang, Qi
Johnson, Philip L F
Braun, Michael J
author_sort Rasband, Shauna A
collection PubMed
description Birds of the order Passeriformes represent the most speciose order of land vertebrates. Despite strong scientific interest in this super-radiation, genetic traits unique to passerines are not well characterized. A duplicate copy of growth hormone (GH) is the only gene known to be present in all major lineages of passerines, but not in other birds. GH genes plausibly influence extreme life history traits that passerines exhibit, including the shortest embryo-to-fledging developmental period of any avian order. To unravel the implications of this GH duplication, we investigated the molecular evolution of the ancestral avian GH gene (GH or GH1) and the novel passerine GH paralog (GH2), using 497 gene sequences extracted from 342 genomes. Passerine GH1 and GH2 are reciprocally monophyletic, consistent with a single duplication event from a microchromosome onto a macrochromosome in a common ancestor of extant passerines. Additional chromosomal rearrangements have changed the syntenic and potential regulatory context of these genes. Both passerine GH1 and GH2 display substantially higher rates of nonsynonymous codon change than non-passerine avian GH, suggesting positive selection following duplication. A site involved in signal peptide cleavage is under selection in both paralogs. Other sites under positive selection differ between the two paralogs, but many are clustered in one region of a 3D model of the protein. Both paralogs retain key functional features and are actively but differentially expressed in two major passerine suborders. These phenomena suggest that GH genes may be evolving novel adaptive roles in passerine birds.
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spelling pubmed-100160472023-03-16 Evolution of the Growth Hormone Gene Duplication in Passerine Birds Rasband, Shauna A Bolton, Peri E Fang, Qi Johnson, Philip L F Braun, Michael J Genome Biol Evol Article Birds of the order Passeriformes represent the most speciose order of land vertebrates. Despite strong scientific interest in this super-radiation, genetic traits unique to passerines are not well characterized. A duplicate copy of growth hormone (GH) is the only gene known to be present in all major lineages of passerines, but not in other birds. GH genes plausibly influence extreme life history traits that passerines exhibit, including the shortest embryo-to-fledging developmental period of any avian order. To unravel the implications of this GH duplication, we investigated the molecular evolution of the ancestral avian GH gene (GH or GH1) and the novel passerine GH paralog (GH2), using 497 gene sequences extracted from 342 genomes. Passerine GH1 and GH2 are reciprocally monophyletic, consistent with a single duplication event from a microchromosome onto a macrochromosome in a common ancestor of extant passerines. Additional chromosomal rearrangements have changed the syntenic and potential regulatory context of these genes. Both passerine GH1 and GH2 display substantially higher rates of nonsynonymous codon change than non-passerine avian GH, suggesting positive selection following duplication. A site involved in signal peptide cleavage is under selection in both paralogs. Other sites under positive selection differ between the two paralogs, but many are clustered in one region of a 3D model of the protein. Both paralogs retain key functional features and are actively but differentially expressed in two major passerine suborders. These phenomena suggest that GH genes may be evolving novel adaptive roles in passerine birds. Oxford University Press 2023-02-27 /pmc/articles/PMC10016047/ /pubmed/36848146 http://dx.doi.org/10.1093/gbe/evad033 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Rasband, Shauna A
Bolton, Peri E
Fang, Qi
Johnson, Philip L F
Braun, Michael J
Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title_full Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title_fullStr Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title_full_unstemmed Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title_short Evolution of the Growth Hormone Gene Duplication in Passerine Birds
title_sort evolution of the growth hormone gene duplication in passerine birds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016047/
https://www.ncbi.nlm.nih.gov/pubmed/36848146
http://dx.doi.org/10.1093/gbe/evad033
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