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Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers

BACKGROUND: Canine hip dysplasia (CHD) is characterised by a malformation of the hip joint, leading to osteoarthritis and lameness. Current breeding schemes against CHD have resulted in measurable but moderate responses. The application of marker-assisted selection, incorporating specific markers as...

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Autores principales: Sánchez-Molano, Enrique, Woolliams, John A, Pong-Wong, Ricardo, Clements, Dylan N, Blott, Sarah C, Wiener, Pamela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190382/
https://www.ncbi.nlm.nih.gov/pubmed/25270232
http://dx.doi.org/10.1186/1471-2164-15-833
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author Sánchez-Molano, Enrique
Woolliams, John A
Pong-Wong, Ricardo
Clements, Dylan N
Blott, Sarah C
Wiener, Pamela
author_facet Sánchez-Molano, Enrique
Woolliams, John A
Pong-Wong, Ricardo
Clements, Dylan N
Blott, Sarah C
Wiener, Pamela
author_sort Sánchez-Molano, Enrique
collection PubMed
description BACKGROUND: Canine hip dysplasia (CHD) is characterised by a malformation of the hip joint, leading to osteoarthritis and lameness. Current breeding schemes against CHD have resulted in measurable but moderate responses. The application of marker-assisted selection, incorporating specific markers associated with the disease, or genomic selection, incorporating genome-wide markers, has the potential to dramatically improve results of breeding schemes. Our aims were to identify regions associated with hip dysplasia or its related traits using genome and chromosome-wide analysis, study the linkage disequilibrium (LD) in these regions and provide plausible gene candidates. This study is focused on the UK Labrador Retriever population, which has a high prevalence of the disease and participates in a recording program led by the British Veterinary Association (BVA) and The Kennel Club (KC). RESULTS: Two genome-wide and several chromosome-wide QTLs affecting CHD and its related traits were identified, indicating regions related to hip dysplasia. CONCLUSION: Consistent with previous studies, the genetic architecture of CHD appears to be based on many genes with small or moderate effect, suggesting that genomic selection rather than marker-assisted selection may be an appropriate strategy for reducing this disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-833) contains supplementary material, which is available to authorized users.
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spelling pubmed-41903822014-10-10 Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers Sánchez-Molano, Enrique Woolliams, John A Pong-Wong, Ricardo Clements, Dylan N Blott, Sarah C Wiener, Pamela BMC Genomics Research Article BACKGROUND: Canine hip dysplasia (CHD) is characterised by a malformation of the hip joint, leading to osteoarthritis and lameness. Current breeding schemes against CHD have resulted in measurable but moderate responses. The application of marker-assisted selection, incorporating specific markers associated with the disease, or genomic selection, incorporating genome-wide markers, has the potential to dramatically improve results of breeding schemes. Our aims were to identify regions associated with hip dysplasia or its related traits using genome and chromosome-wide analysis, study the linkage disequilibrium (LD) in these regions and provide plausible gene candidates. This study is focused on the UK Labrador Retriever population, which has a high prevalence of the disease and participates in a recording program led by the British Veterinary Association (BVA) and The Kennel Club (KC). RESULTS: Two genome-wide and several chromosome-wide QTLs affecting CHD and its related traits were identified, indicating regions related to hip dysplasia. CONCLUSION: Consistent with previous studies, the genetic architecture of CHD appears to be based on many genes with small or moderate effect, suggesting that genomic selection rather than marker-assisted selection may be an appropriate strategy for reducing this disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-833) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-01 /pmc/articles/PMC4190382/ /pubmed/25270232 http://dx.doi.org/10.1186/1471-2164-15-833 Text en © Sánchez-Molano et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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
Sánchez-Molano, Enrique
Woolliams, John A
Pong-Wong, Ricardo
Clements, Dylan N
Blott, Sarah C
Wiener, Pamela
Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title_full Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title_fullStr Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title_full_unstemmed Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title_short Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers
title_sort quantitative trait loci mapping for canine hip dysplasia and its related traits in uk labrador retrievers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190382/
https://www.ncbi.nlm.nih.gov/pubmed/25270232
http://dx.doi.org/10.1186/1471-2164-15-833
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