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Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog

BACKGROUND: The New Zealand native frogs, family Leiopelmatidae, are among the most archaic in the world. Leiopelma hochstetteri (Hochstetter’s frog) is a small, semi-aquatic frog with numerous, fragmented populations scattered across New Zealand’s North Island. We characterized a major histocompati...

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Autores principales: Lillie, Mette, Grueber, Catherine E, Sutton, Jolene T, Howitt, Robyn, Bishop, Phillip J, Gleeson, Dianne, Belov, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415247/
https://www.ncbi.nlm.nih.gov/pubmed/25886729
http://dx.doi.org/10.1186/s12862-015-0342-0
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author Lillie, Mette
Grueber, Catherine E
Sutton, Jolene T
Howitt, Robyn
Bishop, Phillip J
Gleeson, Dianne
Belov, Katherine
author_facet Lillie, Mette
Grueber, Catherine E
Sutton, Jolene T
Howitt, Robyn
Bishop, Phillip J
Gleeson, Dianne
Belov, Katherine
author_sort Lillie, Mette
collection PubMed
description BACKGROUND: The New Zealand native frogs, family Leiopelmatidae, are among the most archaic in the world. Leiopelma hochstetteri (Hochstetter’s frog) is a small, semi-aquatic frog with numerous, fragmented populations scattered across New Zealand’s North Island. We characterized a major histocompatibility complex (MHC) class II B gene (DAB) in L. hochstetteri from a spleen transcriptome, and then compared its diversity to neutral microsatellite markers to assess the adaptive genetic diversity of five populations (“evolutionarily significant units”, ESUs). RESULTS: L. hochstetteri possessed very high MHC diversity, with 74 DAB alleles characterized. Extremely high differentiation was observed at the DAB locus, with only two alleles shared between populations, a pattern that was not reflected in the microsatellites. Clustering analysis on putative peptide binding residues of the DAB alleles indicated four functional supertypes, all of which were represented in 4 of 5 populations, albeit at different frequencies. Otawa was an exception to these observations, with only two DAB alleles present. CONCLUSIONS: This study of MHC diversity highlights extreme population differentiation at this functional locus. Supertype differentiation was high among populations, suggesting spatial and/or temporal variation in selection pressures. Low DAB diversity in Otawa may limit this population’s adaptive potential to future pathogenic challenges. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0342-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-44152472015-05-01 Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog Lillie, Mette Grueber, Catherine E Sutton, Jolene T Howitt, Robyn Bishop, Phillip J Gleeson, Dianne Belov, Katherine BMC Evol Biol Research Article BACKGROUND: The New Zealand native frogs, family Leiopelmatidae, are among the most archaic in the world. Leiopelma hochstetteri (Hochstetter’s frog) is a small, semi-aquatic frog with numerous, fragmented populations scattered across New Zealand’s North Island. We characterized a major histocompatibility complex (MHC) class II B gene (DAB) in L. hochstetteri from a spleen transcriptome, and then compared its diversity to neutral microsatellite markers to assess the adaptive genetic diversity of five populations (“evolutionarily significant units”, ESUs). RESULTS: L. hochstetteri possessed very high MHC diversity, with 74 DAB alleles characterized. Extremely high differentiation was observed at the DAB locus, with only two alleles shared between populations, a pattern that was not reflected in the microsatellites. Clustering analysis on putative peptide binding residues of the DAB alleles indicated four functional supertypes, all of which were represented in 4 of 5 populations, albeit at different frequencies. Otawa was an exception to these observations, with only two DAB alleles present. CONCLUSIONS: This study of MHC diversity highlights extreme population differentiation at this functional locus. Supertype differentiation was high among populations, suggesting spatial and/or temporal variation in selection pressures. Low DAB diversity in Otawa may limit this population’s adaptive potential to future pathogenic challenges. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0342-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-13 /pmc/articles/PMC4415247/ /pubmed/25886729 http://dx.doi.org/10.1186/s12862-015-0342-0 Text en © Lillie et al.; licensee BioMed Central . 2015 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
Lillie, Mette
Grueber, Catherine E
Sutton, Jolene T
Howitt, Robyn
Bishop, Phillip J
Gleeson, Dianne
Belov, Katherine
Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title_full Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title_fullStr Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title_full_unstemmed Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title_short Selection on MHC class II supertypes in the New Zealand endemic Hochstetter’s frog
title_sort selection on mhc class ii supertypes in the new zealand endemic hochstetter’s frog
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415247/
https://www.ncbi.nlm.nih.gov/pubmed/25886729
http://dx.doi.org/10.1186/s12862-015-0342-0
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