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Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations

A key characteristic of MHC genes is the persistence of allelic lineages over macroevolutionary periods, often through multiple speciation events. This phenomenon, known as trans-species polymorphism (TSP), is well documented in several major taxonomic groups, but has less frequently been observed i...

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Autores principales: Eimes, John A., Lee, Sang-im, Townsend, Andrea K., Jablonski, Piotr, Nishiumi, Isao, Satta, Yoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5033386/
https://www.ncbi.nlm.nih.gov/pubmed/27658204
http://dx.doi.org/10.1371/journal.pone.0163456
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author Eimes, John A.
Lee, Sang-im
Townsend, Andrea K.
Jablonski, Piotr
Nishiumi, Isao
Satta, Yoko
author_facet Eimes, John A.
Lee, Sang-im
Townsend, Andrea K.
Jablonski, Piotr
Nishiumi, Isao
Satta, Yoko
author_sort Eimes, John A.
collection PubMed
description A key characteristic of MHC genes is the persistence of allelic lineages over macroevolutionary periods, often through multiple speciation events. This phenomenon, known as trans-species polymorphism (TSP), is well documented in several major taxonomic groups, but has less frequently been observed in birds. The order Passeriformes is arguably the most successful terrestrial vertebrate order in terms of diversity of species and ecological range, but the reasons for this success remain unclear. Passerines exhibit the most highly duplicated MHC genes of any major vertebrate taxonomic group, which may generate increased immune response relative to other avian orders with fewer MHC loci. Here, we describe phylogenetic patterns of the MHC IIB in the passerine family Corvidae. Our results indicate wide-spread TSP within this family, with at least four supported MHC IIB allelic lineages that predate speciation by many millions of years. Markov chain Monte Carlo simulations indicate that divergence of these lineages occurred near the time of the divergence of the Passeriformes and other avian orders. We suggest that the current MHC diversity observed in passerines is due in part to the multiple duplication of a single MHC locus, DAB1, early in passerine evolution and that subsequent duplications of these paralogues have contributed to the enormous success of this order by increasing their ability to recognize and mount immune responses to novel pathogens.
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spelling pubmed-50333862016-10-10 Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations Eimes, John A. Lee, Sang-im Townsend, Andrea K. Jablonski, Piotr Nishiumi, Isao Satta, Yoko PLoS One Research Article A key characteristic of MHC genes is the persistence of allelic lineages over macroevolutionary periods, often through multiple speciation events. This phenomenon, known as trans-species polymorphism (TSP), is well documented in several major taxonomic groups, but has less frequently been observed in birds. The order Passeriformes is arguably the most successful terrestrial vertebrate order in terms of diversity of species and ecological range, but the reasons for this success remain unclear. Passerines exhibit the most highly duplicated MHC genes of any major vertebrate taxonomic group, which may generate increased immune response relative to other avian orders with fewer MHC loci. Here, we describe phylogenetic patterns of the MHC IIB in the passerine family Corvidae. Our results indicate wide-spread TSP within this family, with at least four supported MHC IIB allelic lineages that predate speciation by many millions of years. Markov chain Monte Carlo simulations indicate that divergence of these lineages occurred near the time of the divergence of the Passeriformes and other avian orders. We suggest that the current MHC diversity observed in passerines is due in part to the multiple duplication of a single MHC locus, DAB1, early in passerine evolution and that subsequent duplications of these paralogues have contributed to the enormous success of this order by increasing their ability to recognize and mount immune responses to novel pathogens. Public Library of Science 2016-09-22 /pmc/articles/PMC5033386/ /pubmed/27658204 http://dx.doi.org/10.1371/journal.pone.0163456 Text en © 2016 Eimes et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Eimes, John A.
Lee, Sang-im
Townsend, Andrea K.
Jablonski, Piotr
Nishiumi, Isao
Satta, Yoko
Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title_full Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title_fullStr Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title_full_unstemmed Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title_short Early Duplication of a Single MHC IIB Locus Prior to the Passerine Radiations
title_sort early duplication of a single mhc iib locus prior to the passerine radiations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5033386/
https://www.ncbi.nlm.nih.gov/pubmed/27658204
http://dx.doi.org/10.1371/journal.pone.0163456
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