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A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse

BACKGROUND: Curly horses present a variety of curl phenotypes that are associated with various degrees of curliness of coat, mane, tail and ear hairs. Their origin is still a matter of debate and several genetic hypotheses have been formulated to explain the diversity in phenotype, including the com...

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Autores principales: Morgenthaler, Caroline, Diribarne, Mathieu, Capitan, Aurélien, Legendre, Rachel, Saintilan, Romain, Gilles, Maïlys, Esquerré, Diane, Juras, Rytis, Khanshour, Anas, Schibler, Laurent, Cothran, Gus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686958/
https://www.ncbi.nlm.nih.gov/pubmed/29141579
http://dx.doi.org/10.1186/s12711-017-0359-5
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author Morgenthaler, Caroline
Diribarne, Mathieu
Capitan, Aurélien
Legendre, Rachel
Saintilan, Romain
Gilles, Maïlys
Esquerré, Diane
Juras, Rytis
Khanshour, Anas
Schibler, Laurent
Cothran, Gus
author_facet Morgenthaler, Caroline
Diribarne, Mathieu
Capitan, Aurélien
Legendre, Rachel
Saintilan, Romain
Gilles, Maïlys
Esquerré, Diane
Juras, Rytis
Khanshour, Anas
Schibler, Laurent
Cothran, Gus
author_sort Morgenthaler, Caroline
collection PubMed
description BACKGROUND: Curly horses present a variety of curl phenotypes that are associated with various degrees of curliness of coat, mane, tail and ear hairs. Their origin is still a matter of debate and several genetic hypotheses have been formulated to explain the diversity in phenotype, including the combination of autosomal dominant and recessive alleles. Our purpose was to map the autosomal dominant curly hair locus and identify the causal variant using genome-wide association study (GWAS) and whole-genome sequencing approaches. RESULTS: A GWAS was performed using a Bayesian sparse linear mixed model, based on 51 curly and 19 straight-haired French and North American horses from 13 paternal families genotyped on the Illumina EquineSNP50 BeadChip. A single strong signal was observed on equine chromosome 11, in a region that encompasses the type I keratin gene cluster. This region was refined by haplotype analysis to a segment including 36 genes, among which are 10 keratin genes (KRT-10, -12, -20, -23, -24, -25, -26, -27, -28, -222). To comprehensively identify candidate causal variants within all these genes, whole-genome sequences were obtained for one heterozygous curly stallion and its straight-haired son. Among the four non-synonymous candidate variants identified and validated in the curly region, only variant g.21891160G>A in the KRT25 gene (KRT25:p.R89H) was in perfect agreement with haplotype status in the whole pedigree. Genetic association was then confirmed by genotyping a larger population consisting of 353 horses. However, five discordant curly horses were observed, which carried neither the variant nor the main haplotype associated with curliness. Sequencing of KRT25 for two discordant horses did not identify any other deleterious variant, which suggests locus rather than allelic heterogeneity for the curly phenotype. CONCLUSIONS: We identified the KRT25:p.R89H variant as responsible for the dominant curly trait, but a second dominant locus may also be involved in the shape of hairs within North American Curly horses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12711-017-0359-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-56869582017-11-21 A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse Morgenthaler, Caroline Diribarne, Mathieu Capitan, Aurélien Legendre, Rachel Saintilan, Romain Gilles, Maïlys Esquerré, Diane Juras, Rytis Khanshour, Anas Schibler, Laurent Cothran, Gus Genet Sel Evol Research Article BACKGROUND: Curly horses present a variety of curl phenotypes that are associated with various degrees of curliness of coat, mane, tail and ear hairs. Their origin is still a matter of debate and several genetic hypotheses have been formulated to explain the diversity in phenotype, including the combination of autosomal dominant and recessive alleles. Our purpose was to map the autosomal dominant curly hair locus and identify the causal variant using genome-wide association study (GWAS) and whole-genome sequencing approaches. RESULTS: A GWAS was performed using a Bayesian sparse linear mixed model, based on 51 curly and 19 straight-haired French and North American horses from 13 paternal families genotyped on the Illumina EquineSNP50 BeadChip. A single strong signal was observed on equine chromosome 11, in a region that encompasses the type I keratin gene cluster. This region was refined by haplotype analysis to a segment including 36 genes, among which are 10 keratin genes (KRT-10, -12, -20, -23, -24, -25, -26, -27, -28, -222). To comprehensively identify candidate causal variants within all these genes, whole-genome sequences were obtained for one heterozygous curly stallion and its straight-haired son. Among the four non-synonymous candidate variants identified and validated in the curly region, only variant g.21891160G>A in the KRT25 gene (KRT25:p.R89H) was in perfect agreement with haplotype status in the whole pedigree. Genetic association was then confirmed by genotyping a larger population consisting of 353 horses. However, five discordant curly horses were observed, which carried neither the variant nor the main haplotype associated with curliness. Sequencing of KRT25 for two discordant horses did not identify any other deleterious variant, which suggests locus rather than allelic heterogeneity for the curly phenotype. CONCLUSIONS: We identified the KRT25:p.R89H variant as responsible for the dominant curly trait, but a second dominant locus may also be involved in the shape of hairs within North American Curly horses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12711-017-0359-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-15 /pmc/articles/PMC5686958/ /pubmed/29141579 http://dx.doi.org/10.1186/s12711-017-0359-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Morgenthaler, Caroline
Diribarne, Mathieu
Capitan, Aurélien
Legendre, Rachel
Saintilan, Romain
Gilles, Maïlys
Esquerré, Diane
Juras, Rytis
Khanshour, Anas
Schibler, Laurent
Cothran, Gus
A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title_full A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title_fullStr A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title_full_unstemmed A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title_short A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
title_sort missense variant in the coil1a domain of the keratin 25 gene is associated with the dominant curly hair coat trait (crd) in horse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686958/
https://www.ncbi.nlm.nih.gov/pubmed/29141579
http://dx.doi.org/10.1186/s12711-017-0359-5
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