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Equine veterinary journal1998; 30(1); 13-17; doi: 10.1111/j.2042-3306.1998.tb04083.x

Horse genome mapping: a new era in horse genetics?

Abstract: This research study discusses the importance of creating a gene map for horses to enhance understanding of horse genetics, improve selective breeding methods, and aid in the diagnosis and treatment […]
Publication Date: 1998-02-12 PubMed ID: 9458394DOI: 10.1111/j.2042-3306.1998.tb04083.xGoogle Scholar: Lookup
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Summary

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This research study discusses the importance of creating a gene map for horses to enhance understanding of horse genetics, improve selective breeding methods, and aid in the diagnosis and treatment of inherited diseases in horses.

Horse Genetics and Selective Breeding

  • This paper notes that despite the lengthy history of stud books tracing horse breeds back over two centuries, the study of horse genetics remains less advanced than that of other companion and domestic animals.
  • Genetic variation forms the basis of variations in performance and appearance across horse breeds.
  • In the realm of selective breeding, this natural genetic variation is used to enhance specific characteristics in horses. However, the existing selective breeding practices have been deemed inefficient, and their enhancement could be achieved with a more in-depth understanding of the genetic markers associated with desirable traits.

The Importance of a Horse Genome Map

  • A genome map, already published for many species such as humans, mice, cows, pigs, sheep, and chickens, is identified as an important tool in studying any species’ genetics.
  • The paper suggests that a horse genome map would assist in examining genetic components linked to inherited diseases, performance factors, physical conformation, and fertility issues.
  • The paper further suggests potential applications, such as identifying markers linked to various conditions, including osteochondrosis. This could lead to the development of genetic screening tests for many inherited diseases, including chronic obstructive pulmonary disease (COPD), rhabdomyolysis (tying up), and laryngeal hemiplegia (roaring), among others.

Molecular Genetic Studies and Implications

  • There has been a recent surge in molecular genetic studies of horses, potentially providing the tools to analyze a broad range of inherited diseases and traits in horses and other Equidae.
  • The research could have a substantial impact on diagnosing and treating inherited horse diseases, as well as on the selection policies implemented by horse breeders.
  • The study emphasizes the important role of the equine veterinarian in identifying genetically controlled traits and in sourcing blood samples.
  • Research is hampered by insufficient knowledge and resources. Frequently, questions about whether a trait is inherited in horses go unanswered. Resource families with horses displaying interesting conditions are vital for mapping genes involved in various traits.
  • The study concludes with a call to action: the collection of samples and identification of suitable pedigrees should be accelerated to ensure the ready availability of these samples when the genetic map for horses is completed.

Cite This Article

APA
Marti E, Binns M. (1998). Horse genome mapping: a new era in horse genetics? Equine Vet J, 30(1), 13-17. https://doi.org/10.1111/j.2042-3306.1998.tb04083.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 30
Issue: 1
Pages: 13-17

Researcher Affiliations

Marti, E
  • Institute for Animal Breeding, University of Berne, Switzerland.
Binns, M

    MeSH Terms

    • Animals
    • Chromosome Mapping / methods
    • Chromosome Mapping / veterinary
    • Genetic Diseases, Inborn / genetics
    • Genetic Diseases, Inborn / veterinary
    • Genetic Markers / genetics
    • Genome
    • Horses / genetics
    • Pedigree

    Citations

    This article has been cited 1 times.
    1. Chowdhary BP, Raudsepp T. The horse genome derby: racing from map to whole genome sequence. Chromosome Res 2008;16(1):109-27.
      doi: 10.1007/s10577-008-1204-zpubmed: 18274866google scholar: lookup