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High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system

BACKGROUND: The genes of the major histocompatibility complex (MHC/MH) have attracted considerable scientific interest due to their exceptional levels of variability and important function as part of the adaptive immune system. Despite a large number of studies on MH class II diversity of both model...

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Autores principales: Wilson, Anthony B, Whittington, Camilla M, Bahr, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302578/
https://www.ncbi.nlm.nih.gov/pubmed/25526691
http://dx.doi.org/10.1186/s12862-014-0273-1
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author Wilson, Anthony B
Whittington, Camilla M
Bahr, Angela
author_facet Wilson, Anthony B
Whittington, Camilla M
Bahr, Angela
author_sort Wilson, Anthony B
collection PubMed
description BACKGROUND: The genes of the major histocompatibility complex (MHC/MH) have attracted considerable scientific interest due to their exceptional levels of variability and important function as part of the adaptive immune system. Despite a large number of studies on MH class II diversity of both model and non-model organisms, most research has focused on patterns of genetic variability at individual loci, failing to capture the functional diversity of the biologically active dimeric molecule. Here, we take a systematic approach to the study of MH variation, analyzing patterns of genetic variation at MH class IIα and IIβ loci of the seahorse, which together form the immunologically active peptide binding cleft of the MH class II molecule. RESULTS: The seahorse carries a minimal class II system, consisting of single copies of both MH class IIα and IIβ, which are physically linked and inherited in a Mendelian fashion. Both genes are ubiquitously expressed and detectible in the brood pouch of male seahorses throughout pregnancy. Genetic variability of the two genes is high, dominated by non-synonymous variation concentrated in their peptide-binding regions. Coding variation outside these regions is negligible, a pattern thought to be driven by intra- and interlocus recombination. Despite the tight physical linkage of MH IIα and IIβ loci, recombination has produced novel composite alleles, increasing functional diversity at sites responsible for antigen recognition. CONCLUSIONS: Antigen recognition by the adaptive immune system of the seahorse is enhanced by high variability at both MH class IIα and IIβ loci. Strong positive selection on sites involved in pathogen recognition, coupled with high levels of intra- and interlocus recombination, produce a patchwork pattern of genetic variation driven by genetic hitchhiking. Studies focusing on variation at individual MH loci may unintentionally overlook an important component of ecologically relevant variation.
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spelling pubmed-43025782015-01-23 High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system Wilson, Anthony B Whittington, Camilla M Bahr, Angela BMC Evol Biol Research Article BACKGROUND: The genes of the major histocompatibility complex (MHC/MH) have attracted considerable scientific interest due to their exceptional levels of variability and important function as part of the adaptive immune system. Despite a large number of studies on MH class II diversity of both model and non-model organisms, most research has focused on patterns of genetic variability at individual loci, failing to capture the functional diversity of the biologically active dimeric molecule. Here, we take a systematic approach to the study of MH variation, analyzing patterns of genetic variation at MH class IIα and IIβ loci of the seahorse, which together form the immunologically active peptide binding cleft of the MH class II molecule. RESULTS: The seahorse carries a minimal class II system, consisting of single copies of both MH class IIα and IIβ, which are physically linked and inherited in a Mendelian fashion. Both genes are ubiquitously expressed and detectible in the brood pouch of male seahorses throughout pregnancy. Genetic variability of the two genes is high, dominated by non-synonymous variation concentrated in their peptide-binding regions. Coding variation outside these regions is negligible, a pattern thought to be driven by intra- and interlocus recombination. Despite the tight physical linkage of MH IIα and IIβ loci, recombination has produced novel composite alleles, increasing functional diversity at sites responsible for antigen recognition. CONCLUSIONS: Antigen recognition by the adaptive immune system of the seahorse is enhanced by high variability at both MH class IIα and IIβ loci. Strong positive selection on sites involved in pathogen recognition, coupled with high levels of intra- and interlocus recombination, produce a patchwork pattern of genetic variation driven by genetic hitchhiking. Studies focusing on variation at individual MH loci may unintentionally overlook an important component of ecologically relevant variation. BioMed Central 2014-12-20 /pmc/articles/PMC4302578/ /pubmed/25526691 http://dx.doi.org/10.1186/s12862-014-0273-1 Text en © Wilson et al.; licensee BioMed Central. 2014 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wilson, Anthony B
Whittington, Camilla M
Bahr, Angela
High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title_full High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title_fullStr High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title_full_unstemmed High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title_short High intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
title_sort high intralocus variability and interlocus recombination promote immunological diversity in a minimal major histocompatibility system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302578/
https://www.ncbi.nlm.nih.gov/pubmed/25526691
http://dx.doi.org/10.1186/s12862-014-0273-1
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