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Genome1990; 33(5); 679-682; doi: 10.1139/g90-101

Two autosomal trisomies in the horse: 64,XX,-26,+t(26q26q) and 65,XX,+30.

Abstract: The phenotypic effects in a yearling Arab filly of a newly described equine autosomal trisomy syndrome for chromosome 30 (65,XX,+30) consisted of small size and severe angular deviation of front legs accompanied by mild polydactyly, but no mental dullness. This case was associated with advanced maternal age. Additional banding studies of a second trisomy case confirmed the assignment to chromosome 26 (64,XX,-26,+t(26q26q)) and evidence of her fertility was presented.
Publication Date: 1990-10-01 PubMed ID: 2262139DOI: 10.1139/g90-101Google Scholar: Lookup
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Summary

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This study examines two new equine chromosomal disorders in horses. A syndrome related to the trisomy (an extra chromosome) of chromosome 30 caused small size and abnormal leg formation in a young Arab filly, while another trisomy relating to chromosome 26 was evidenced in a different horse.

Understanding the Research Abstract

  • The research revolves around two newly discovered equine chromosomal disorders found in horses. The conditions are related to a phenomenon known as trisomy, which happens when an organism has three rather than the usual two copies of a particular chromosome.
  • The first condition, identified as an autosomal trisomy for chromosome 30 (65,XX,+30) in a yearling (one-year-old) Arab filly, led to the horse being smaller than average and having severe angular deviations in the front legs, along with mild polydactyly (having more than the normal number of toes). Interestingly, there was no evidence of cognitive impairment or mental dullness in the horse. It was also observed that this case was associated with the mother of the horse being of advanced age.
  • The second case of trisomy related to chromosome 26 (64,XX,-26,+t(26q26q)) was confirmed through additional banding studies, a technique used for identifying chromosomes. The research presents evidence of the horse’s fertility despite this trisomy.

Implications of the Research

  • The findings enhance our understanding of equine genetics and the impact of chromosomal disorders on physical characteristics and health in horses. Though the identified syndromes have different effects, they could both significantly impact a horse’s health, physical development, and reproductive capabilities.
  • These findings could also lead to more thorough genetic screening practices in breeding horses, allowing breeders to identify and manage these conditions at their onset.
  • While chromosomal disorders are common in many organisms, not much is known about these conditions in horses. By studying these trisomy cases, researchers can learn more about equine genetics, potentially leading to better treatment options for these and similar conditions.

Cite This Article

APA
Bowling AT, Millon LV. (1990). Two autosomal trisomies in the horse: 64,XX,-26,+t(26q26q) and 65,XX,+30. Genome, 33(5), 679-682. https://doi.org/10.1139/g90-101

Publication

ISSN: 0831-2796
NlmUniqueID: 8704544
Country: Canada
Language: English
Volume: 33
Issue: 5
Pages: 679-682

Researcher Affiliations

Bowling, A T
  • Serology Laboratory, University of California, School of Veterinary Medicine, Davis 95616.
Millon, L V

    MeSH Terms

    • Animals
    • Chromosome Aberrations
    • Chromosome Banding
    • Female
    • Horses / genetics
    • Karyotyping
    • Phenotype
    • Trisomy

    Citations

    This article has been cited 7 times.
    1. Ghosh S, Kjöllerström J, Metcalfe L, Reed S, Juras R, Raudsepp T. The Second Case of Non-Mosaic Trisomy of Chromosome 26 with Homologous Fusion 26q;26q in the Horse. Animals (Basel) 2022 Mar 22;12(7).
      doi: 10.3390/ani12070803pubmed: 35405793google scholar: lookup
    2. Bugno-Poniewierska M, Raudsepp T. Horse Clinical Cytogenetics: Recurrent Themes and Novel Findings. Animals (Basel) 2021 Mar 16;11(3).
      doi: 10.3390/ani11030831pubmed: 33809432google scholar: lookup
    3. Shilton CA, Kahler A, Davis BW, Crabtree JR, Crowhurst J, McGladdery AJ, Wathes DC, Raudsepp T, de Mestre AM. Whole genome analysis reveals aneuploidies in early pregnancy loss in the horse. Sci Rep 2020 Aug 7;10(1):13314.
      doi: 10.1038/s41598-020-69967-zpubmed: 32769994google scholar: lookup
    4. Bowling AT, Breen M, Chowdhary BP, Hirota K, Lear T, Millon LV, Ponce de Leon FA, Raudsepp T, Stranzinger G. International system for cytogenetic nomenclature of the domestic horse. Report of the Third International Committee for the Standardization of the domestic horse karyotype, Davis, CA, USA, 1996. Chromosome Res 1997 Nov;5(7):433-43.
      doi: 10.1023/a:1018408811881pubmed: 9421259google scholar: lookup
    5. Bowling AT, Millon LV, Dileanis S. Physical mapping of genetic markers to chromosome 30 using a trisomic horse and evidence for maternal origin of the extra chromosome. Chromosome Res 1997 Sep;5(6):429-31.
      doi: 10.1023/a:1018456727811pubmed: 9364945google scholar: lookup
    6. Ryan CA, Berry DP, Bugno-Poniewierska M, Burke MK, Raudsepp T, Egan S, Doyle JL. Two Cases of Chromosome 27 Trisomy in Horses Detected Using Illumina BeadChip Genotyping. Animals (Basel) 2025 Jun 22;15(13).
      doi: 10.3390/ani15131842pubmed: 40646741google scholar: lookup
    7. Baville E, Carstanjen B, Thomas-Cancian A, Calgaro A, Bonnet N, Tiret L, Gache V, Abitbol M. Inherited non-syndromic polydactyly in a Berber and Arabian-Berber horse family. Equine Vet J 2025 Nov;57(6):1511-1519.
      doi: 10.1111/evj.14472pubmed: 39853805google scholar: lookup