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Animal genetics1987; 18(2); 181-186; doi: 10.1111/j.1365-2052.1987.tb00757.x

Frequencies of plasma protease inhibitor alleles in Australian horse breeds and the recognition of two new alleles.

Abstract: Investigation of the plasma protease inhibitor system (Pi) in the Arabian and quarter horse breeds and re-examination of the standardbred breed resulted in the recognition of two new Pi alleles, designated E and L2. PiE is rare and has been found in only three quarter horses. In contrast, PiL2 is relatively common in the standardbred (0.107) and allowed subdivision of PiL into PiL and PiL2. Splitting of PiL resulted in an exclusion probability (PE) of 0.649 for the standardbred Pi system. Frequencies of the Pi genes have now been determined for four breeds (thoroughbred, standardbred, quarter horse and Arabian) of horses in Australia.
Publication Date: 1987-01-01 PubMed ID: 3662117DOI: 10.1111/j.1365-2052.1987.tb00757.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article examines different genetic variants (alleles) of a blood component (plasma protease inhibitor) in various horse breeds in Australia, where two new alleles were discovered.

Understanding the Plasma Protease Inhibitor (Pi) System

  • The plasma protease inhibitor (Pi) system is a genetic system present in horses that influences the blood’s ability to clot in response to injury or disease.
  • The researchers were investigating differences in this system across different breeds of horses, specifically focusing on the Arabian, quarter horse, and standardbred breeds.

Identification of New Pi Alleles

  • Through their investigation, they identified two new alleles, or variants, of the Pi system. These have been named PiE and PiL2.
  • PiE is considered rare, as it has only been found in three quarter horses, while the PiL2 variant was found to be quite common in standardbred horses.
  • The discovery of these new alleles allows for more detailed understanding and categorization of the Pi system across different horse breeds.

Implications for the Standardbred Pi System

  • The identification of the PiL2 allele led to a subdivision of the existing PiL category into PiL and PiL2.
  • This subdivision resulted in an exclusion probability (PE) of 0.649 for the standardbred Pi system, meaning that there’s a 64.9% chance that a randomly selected allele from the population would not be the specific PiL allele. This high exclusion probability indicates a significant level of genetic diversity within the standardbred breed’s Pi system.

Further Pi Gene Frequency Exploration

  • The research extends beyond the initial breeds, with the authors having now determined the frequencies of the Pi genes across four different horse breeds in Australia – thoroughbred, standardbred, quarter horse, and Arabian.
  • Knowing the specific frequency of these genes in each breed provides valuable information about how common specific alleles are, and may aid in breed identification and the understanding of genetic disease risk.

Cite This Article

APA
Patterson SD, Bell K. (1987). Frequencies of plasma protease inhibitor alleles in Australian horse breeds and the recognition of two new alleles. Anim Genet, 18(2), 181-186. https://doi.org/10.1111/j.1365-2052.1987.tb00757.x

Publication

ISSN: 0268-9146
NlmUniqueID: 8605704
Country: England
Language: English
Volume: 18
Issue: 2
Pages: 181-186

Researcher Affiliations

Patterson, S D
  • Department of Physiology and Pharmacology, University of Queensland, St Lucia, Australia.
Bell, K

    MeSH Terms

    • Alleles
    • Animals
    • Australia
    • Crosses, Genetic
    • Female
    • Gene Frequency
    • Horses / genetics
    • Male
    • Protease Inhibitors / blood
    • Protease Inhibitors / genetics
    • Species Specificity

    Citations

    This article has been cited 1 times.
    1. Patterson SD, Bell K, Shaw DC. The equine major plasma serpin multigene family: partial characterization including sequence of the reactive-site regions. Biochem Genet 1991 Oct;29(9-10):477-99.
      doi: 10.1007/BF02399689pubmed: 1772402google scholar: lookup