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Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes

Genes of the immune system are generally considered to evolve rapidly due to host–parasite coevolution. They are therefore of great interest in evolutionary biology and molecular ecology. In this study, we manually annotated 144 avian immune genes from the zebra finch (Taeniopygia guttata) genome an...

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Autores principales: Ekblom, Robert, French, Lisa, Slate, Jon, Burke, Terry
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975445/
https://www.ncbi.nlm.nih.gov/pubmed/20884724
http://dx.doi.org/10.1093/gbe/evq061
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author Ekblom, Robert
French, Lisa
Slate, Jon
Burke, Terry
author_facet Ekblom, Robert
French, Lisa
Slate, Jon
Burke, Terry
author_sort Ekblom, Robert
collection PubMed
description Genes of the immune system are generally considered to evolve rapidly due to host–parasite coevolution. They are therefore of great interest in evolutionary biology and molecular ecology. In this study, we manually annotated 144 avian immune genes from the zebra finch (Taeniopygia guttata) genome and conducted evolutionary analyses of these by comparing them with their orthologs in the chicken (Gallus gallus). Genes classified as immune receptors showed elevated d(N)/d(S) ratios compared with other classes of immune genes. Immune genes in general also appear to be evolving more rapidly than other genes, as inferred from a higher d(N)/d(S) ratio compared with the rest of the genome. Furthermore, ten genes (of 27) for which sequence data were available from at least three bird species showed evidence of positive selection acting on specific codons. From transcriptome data of eight different tissues, we found evidence for expression of 106 of the studied immune genes, with primary expression of most of these in bursa, blood, and spleen. These immune-related genes showed a more tissue-specific expression pattern than other genes in the zebra finch genome. Several of the avian immune genes investigated here provide strong candidates for in-depth studies of molecular adaptation in birds.
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spelling pubmed-29754452010-11-08 Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes Ekblom, Robert French, Lisa Slate, Jon Burke, Terry Genome Biol Evol Research Articles Genes of the immune system are generally considered to evolve rapidly due to host–parasite coevolution. They are therefore of great interest in evolutionary biology and molecular ecology. In this study, we manually annotated 144 avian immune genes from the zebra finch (Taeniopygia guttata) genome and conducted evolutionary analyses of these by comparing them with their orthologs in the chicken (Gallus gallus). Genes classified as immune receptors showed elevated d(N)/d(S) ratios compared with other classes of immune genes. Immune genes in general also appear to be evolving more rapidly than other genes, as inferred from a higher d(N)/d(S) ratio compared with the rest of the genome. Furthermore, ten genes (of 27) for which sequence data were available from at least three bird species showed evidence of positive selection acting on specific codons. From transcriptome data of eight different tissues, we found evidence for expression of 106 of the studied immune genes, with primary expression of most of these in bursa, blood, and spleen. These immune-related genes showed a more tissue-specific expression pattern than other genes in the zebra finch genome. Several of the avian immune genes investigated here provide strong candidates for in-depth studies of molecular adaptation in birds. Oxford University Press 2010 2010-09-30 /pmc/articles/PMC2975445/ /pubmed/20884724 http://dx.doi.org/10.1093/gbe/evq061 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ekblom, Robert
French, Lisa
Slate, Jon
Burke, Terry
Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title_full Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title_fullStr Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title_full_unstemmed Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title_short Evolutionary Analysis and Expression Profiling of Zebra Finch Immune Genes
title_sort evolutionary analysis and expression profiling of zebra finch immune genes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975445/
https://www.ncbi.nlm.nih.gov/pubmed/20884724
http://dx.doi.org/10.1093/gbe/evq061
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