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Evolution of MHC class I genes in the European badger (Meles meles)
The major histocompatibility complex (MHC) plays a central role in the adaptive immune system and provides a good model with which to understand the evolutionary processes underlying functional genes. Trans-species polymorphism and orthology are both commonly found in MHC genes; however, mammalian M...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434948/ https://www.ncbi.nlm.nih.gov/pubmed/22957169 http://dx.doi.org/10.1002/ece3.285 |
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author | Sin, Yung Wa Dugdale, Hannah L Newman, Chris Macdonald, David W Burke, Terry |
author_facet | Sin, Yung Wa Dugdale, Hannah L Newman, Chris Macdonald, David W Burke, Terry |
author_sort | Sin, Yung Wa |
collection | PubMed |
description | The major histocompatibility complex (MHC) plays a central role in the adaptive immune system and provides a good model with which to understand the evolutionary processes underlying functional genes. Trans-species polymorphism and orthology are both commonly found in MHC genes; however, mammalian MHC class I genes tend to cluster by species. Concerted evolution has the potential to homogenize different loci, whereas birth-and-death evolution can lead to the loss of orthologs; both processes result in monophyletic groups within species. Studies investigating the evolution of MHC class I genes have been biased toward a few particular taxa and model species. We present the first study of MHC class I genes in a species from the superfamily Musteloidea. The European badger (Meles meles) exhibits moderate variation in MHC class I sequences when compared to other carnivores. We identified seven putatively functional sequences and nine pseudogenes from genomic (gDNA) and complementary (cDNA) DNA, signifying at least two functional class I loci. We found evidence for separate evolutionary histories of the α1 and α2/α3 domains. In the α1 domain, several sequences from different species were more closely related to each other than to sequences from the same species, resembling orthology or trans-species polymorphism. Balancing selection and probable recombination maintain genetic diversity in the α1 domain, evidenced by the detection of positive selection and a recombination event. By comparison, two recombination breakpoints indicate that the α2/α3 domains have most likely undergone concerted evolution, where recombination has homogenized the α2/α3 domains between genes, leading to species-specific clusters of sequences. Our findings highlight the importance of analyzing MHC domains separately. |
format | Online Article Text |
id | pubmed-3434948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34349482012-09-06 Evolution of MHC class I genes in the European badger (Meles meles) Sin, Yung Wa Dugdale, Hannah L Newman, Chris Macdonald, David W Burke, Terry Ecol Evol Original Research The major histocompatibility complex (MHC) plays a central role in the adaptive immune system and provides a good model with which to understand the evolutionary processes underlying functional genes. Trans-species polymorphism and orthology are both commonly found in MHC genes; however, mammalian MHC class I genes tend to cluster by species. Concerted evolution has the potential to homogenize different loci, whereas birth-and-death evolution can lead to the loss of orthologs; both processes result in monophyletic groups within species. Studies investigating the evolution of MHC class I genes have been biased toward a few particular taxa and model species. We present the first study of MHC class I genes in a species from the superfamily Musteloidea. The European badger (Meles meles) exhibits moderate variation in MHC class I sequences when compared to other carnivores. We identified seven putatively functional sequences and nine pseudogenes from genomic (gDNA) and complementary (cDNA) DNA, signifying at least two functional class I loci. We found evidence for separate evolutionary histories of the α1 and α2/α3 domains. In the α1 domain, several sequences from different species were more closely related to each other than to sequences from the same species, resembling orthology or trans-species polymorphism. Balancing selection and probable recombination maintain genetic diversity in the α1 domain, evidenced by the detection of positive selection and a recombination event. By comparison, two recombination breakpoints indicate that the α2/α3 domains have most likely undergone concerted evolution, where recombination has homogenized the α2/α3 domains between genes, leading to species-specific clusters of sequences. Our findings highlight the importance of analyzing MHC domains separately. Blackwell Publishing Ltd 2012-07 /pmc/articles/PMC3434948/ /pubmed/22957169 http://dx.doi.org/10.1002/ece3.285 Text en © 2012 The Authors. Published by Blackwell Publishing Ltd. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Research Sin, Yung Wa Dugdale, Hannah L Newman, Chris Macdonald, David W Burke, Terry Evolution of MHC class I genes in the European badger (Meles meles) |
title | Evolution of MHC class I genes in the European badger (Meles meles) |
title_full | Evolution of MHC class I genes in the European badger (Meles meles) |
title_fullStr | Evolution of MHC class I genes in the European badger (Meles meles) |
title_full_unstemmed | Evolution of MHC class I genes in the European badger (Meles meles) |
title_short | Evolution of MHC class I genes in the European badger (Meles meles) |
title_sort | evolution of mhc class i genes in the european badger (meles meles) |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434948/ https://www.ncbi.nlm.nih.gov/pubmed/22957169 http://dx.doi.org/10.1002/ece3.285 |
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