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Animal genetics2009; 40(4); 553-555; doi: 10.1111/j.1365-2052.2009.01865.x

Refinement of a quantitative trait locus on equine chromosome 5 responsible for fetlock osteochondrosis in Hanoverian warmblood horses.

Abstract: In this report, we provide 29 new informative microsatellites distributed over a region of 21 Mb on horse chromosome (ECA) 5 and refine a quantitative trait locus (QTL) for fetlock osteochondrosis dissecans (OCD) to a genome-wide significant interval between 78.03 and 90.23 Mb on ECA5. Genotyping was performed in 211 Hanoverian warmblood horses from 14 paternal half-sib groups. Within this OCD-QTL, collagen type XXIV alpha 1 was identified as a potential functional candidate gene for equine osteochondrosis. This report is a further step towards unravelling the genes that cause equine osteochondrosis.
Publication Date: 2009-03-20 PubMed ID: 19392821DOI: 10.1111/j.1365-2052.2009.01865.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study elaborates on the identification of a specific region on equine chromosome 5 which is significantly linked to fetlock osteochondrosis, a bone and cartilage disorder in Hanoverian warmblood horses.

Informative Microsatellites and Genotyping

  • The researchers discovered 29 new informative microsatellites. Microsatellites, also known as short tandem repeats (STRs), are sequences in the DNA that repeat over and over again.
  • These repetitive sequences are scattered across a specific region of about 21 million base pairs (Mb) on Horse Chromosome 5 (ECA 5).
  • Genotyping was performed on 211 Hanoverian warmblood horses that were divided into 14 paternal half-sibling groups. Genotyping is a process used to determine differences in the genetic make-up of an individual by examining the individual’s DNA sequence.

Determination of Quantitative Trait Locus (QTL) for Osteochondrosis Dissecans (OCD)

  • The researchers refined a quantitative trait locus (QTL) for osteochondrosis dissecans (OCD). QTL is a region of DNA which correlates with variation in a phenotype. In this case, the variant is the tendency to develop OCD, a joint disorder in horses where fragments of bone and cartilage come loose.
  • This QTL for OCD was found to be a genome-wide significant interval between 78.03 and 90.23 Mb on ECA5. A genome-wide significant interval is a location in the genome which is statistically significantly associated with a trait.

Identification of Potential Functional Candidate Gene

  • Within this QTL for OCD, the researchers singled out ‘collagen type XXIV alpha 1’ as a likely functional candidate gene for equine osteochondrosis. This means that variations in this gene might be the cause of OCD in these horses.
  • However, it’s termed ‘potential’ since further investigation is necessary to confirm its role in the disease.

Significance of the Study

  • This study enhances understanding of genetic factors contributing to equine osteochondrosis thus aiding the development of breeding strategies to minimize occurrence of the disease.
  • The findings represent another step towards identifying the specific genes linked to the onset of equine osteochondrosis, which could lead to the development of effective treatments.

Cite This Article

APA
Lampe V, Dierks C, Distl O. (2009). Refinement of a quantitative trait locus on equine chromosome 5 responsible for fetlock osteochondrosis in Hanoverian warmblood horses. Anim Genet, 40(4), 553-555. https://doi.org/10.1111/j.1365-2052.2009.01865.x

Publication

ISSN: 1365-2052
NlmUniqueID: 8605704
Country: England
Language: English
Volume: 40
Issue: 4
Pages: 553-555

Researcher Affiliations

Lampe, V
  • Institute for Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Bünteweg 17p, 30559 Hannover, Germany.
Dierks, C
    Distl, O

      MeSH Terms

      • Animals
      • Chromosome Mapping
      • Chromosomes, Mammalian
      • Foot Diseases / genetics
      • Foot Diseases / veterinary
      • Genotype
      • Horse Diseases / genetics
      • Horses / genetics
      • Microsatellite Repeats
      • Osteochondrosis / genetics
      • Osteochondrosis / veterinary
      • Quantitative Trait Loci

      Citations

      This article has been cited 4 times.
      1. Martinez-Saez L, Marín-García PJ, Llobat ML. Osteochondrosis in horses: An overview of genetic and other factors. Equine Vet J 2026 Jan;58(1):6-19.
        doi: 10.1111/evj.14518pubmed: 40302410google scholar: lookup
      2. Raudsepp T, Finno CJ, Bellone RR, Petersen JL. Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post-genome era. Anim Genet 2019 Dec;50(6):569-597.
        doi: 10.1111/age.12857pubmed: 31568563google scholar: lookup
      3. Sevane N, Dunner S, Boado A, Cañon J. Polymorphisms in ten candidate genes are associated with conformational and locomotive traits in Spanish Purebred horses. J Appl Genet 2017 Aug;58(3):355-361.
        doi: 10.1007/s13353-016-0385-ypubmed: 27917442google scholar: lookup
      4. Bates JT, Jacobs JC Jr, Shea KG, Oxford JT. Emerging genetic basis of osteochondritis dissecans. Clin Sports Med 2014 Apr;33(2):199-220.
        doi: 10.1016/j.csm.2013.11.004pubmed: 24698039google scholar: lookup