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

Sánchez-Molano, Enrique; Woolliams, John A.; Pong-Wong, Ricardo; Clements, Dylan N.; Blott, Sarah; Wiener, Pamela

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


Authors

Enrique Sánchez-Molano

John A. Woolliams

Ricardo Pong-Wong

Dylan N. Clements

Pamela Wiener



Abstract

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.

Journal Article Type Article
Acceptance Date Sep 23, 2014
Online Publication Date Oct 1, 2014
Publication Date Oct 1, 2014
Deposit Date Oct 11, 2017
Publicly Available Date Jan 25, 2024
Journal BMC Genomics
Electronic ISSN 1471-2164
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 15
Issue 1
Article Number 833
DOI https://doi.org/10.1186/1471-2164-15-833
Public URL https://nottingham-repository.worktribe.com/output/1099936
Publisher URL https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-15-833
PMID 25270232

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