Analyze Diet
The Journal of heredity1987; 78(2); 75-80; doi: 10.1093/oxfordjournals.jhered.a110340

Genetic studies of blood markers in Przewalski’s horses.

Abstract: Ninety-six Przewalski's horses (Equus przewalskii) were blood typed using systems of inherited blood variants known to be highly effective for parentage testing of domestic horses (E. caballus). Sixteen red cell antigenic factors detected using sera prepared by alloimmunization of domestic horses were shown to be inherited in six systems (A, C, D, P, Q, and U) and in the same patterns as domestic horses. Family data confirmed autosomal, codominant inheritance at five loci of serum protein variants (Al, Tf, Xk, Pi, and Es) and three loci of red cell proteins (PGM, PHI, and Hb). One serum protein locus (Gc) and two red cell protein loci (PGD and CA) appeared to be monomorphic. Despite the narrow genetic base and high inbreeding coefficients of captive Przewalski's horses, average heterozygosity calculated over 18 loci was estimated to be 0.320 +/- 0.05, which was similar to that found in five breeds of domestic horses.
Publication Date: 1987-03-01 PubMed ID: 3584938DOI: 10.1093/oxfordjournals.jhered.a110340Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study investigates the genetic aspects of blood markers in the Przewalski’s horse population, using blood typing systems that have been successful in parentage testing of domestic horses. The researchers found that despite the Przewalski’s horses’ limited genetic base and high inbreeding, their average heterozygosity is comparable to that of five domestic horse breeds.

Research Design and Methodology

  • The researchers carried out a blood typing study on a sample size of ninety-six Przewalski’s horses, utilising systems of inherited blood variants that have previously been effective in determining the parentage of domestic horses.
  • They identified sixteen red cell antigenic factors, utilising sera created by alloimmunization (building of immunity) in domestic horses.

Inheritance Patterns

  • The researchers found that these factors were inherited in six systems – A, C, D, P, Q, and U – in similar patterns to those in domestic horses.
  • Analysis of family data showed autosomal and codominant inheritance at eight loci, consisting of five loci of serum protein variants (Al, Tf, Xk, Pi, and Es) and three loci of red cell proteins (PGM, PHI, and Hb).
  • A serum protein locus (Gc) and two red cell protein loci (PGD and CA) seemed to be monomorphic, where they only had one form.

Analysis of Genetic Diversity

  • The researchers analysed the heterozygosity, or genetic diversity, within the Przewalski’s horse population.
  • Despite the small genetic base and high rates of inbreeding of captive populations of these horses, the researchers claim that heterozygosity is relatively high.
  • An average heterozygosity was calculated over eighteen loci, and estimated to be around 0.320 +/- 0.05 – a figure that is comparable to what is found in five different breeds of domestic horses.

Cite This Article

APA
Bowling AT, Ryder OA. (1987). Genetic studies of blood markers in Przewalski’s horses. J Hered, 78(2), 75-80. https://doi.org/10.1093/oxfordjournals.jhered.a110340

Publication

ISSN: 0022-1503
NlmUniqueID: 0375373
Country: United States
Language: English
Volume: 78
Issue: 2
Pages: 75-80

Researcher Affiliations

Bowling, A T
    Ryder, O A

      MeSH Terms

      • Alleles
      • Animals
      • Animals, Wild
      • Blood Group Antigens / genetics
      • Blood Proteins / genetics
      • Erythrocytes / analysis
      • Gene Frequency
      • Horses / blood
      • Horses / genetics
      • Polymorphism, Genetic

      Citations

      This article has been cited 7 times.
      1. Turghan MA, Jiang Z, Niu Z. An Update on Status and Conservation of the Przewalski's Horse (Equus ferus przewalskii): Captive Breeding and Reintroduction Projects. Animals (Basel) 2022 Nov 15;12(22).
        doi: 10.3390/ani12223158pubmed: 36428386google scholar: lookup
      2. Imsland F, McGowan K, Rubin CJ, Henegar C, Sundström E, Berglund J, Schwochow D, Gustafson U, Imsland P, Lindblad-Toh K, Lindgren G, Mikko S, Millon L, Wade C, Schubert M, Orlando L, Penedo MC, Barsh GS, Andersson L. Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses. Nat Genet 2016 Feb;48(2):152-8.
        doi: 10.1038/ng.3475pubmed: 26691985google scholar: lookup
      3. Chen J, Weng Q, Chao J, Hu D, Taya K. Reproduction and Development of the Released Przewalski's Horses (Equus przewalskii) in Xinjiang, China. J Equine Sci 2008;19(1):1-7.
        doi: 10.1294/jes.19.1pubmed: 24833949google scholar: lookup
      4. Gupta AK, Chauhan M, Bhardwaj A. Genetic diversity and bottleneck studies in endangered Bhutia and Manipuri pony breeds. Mol Biol Rep 2013 Dec;40(12):6935-43.
        doi: 10.1007/s11033-013-2813-ypubmed: 24150726google scholar: lookup
      5. Goto H, Ryder OA, Fisher AR, Schultz B, Kosakovsky Pond SL, Nekrutenko A, Makova KD. A massively parallel sequencing approach uncovers ancient origins and high genetic variability of endangered Przewalski's horses. Genome Biol Evol 2011;3:1096-106.
        doi: 10.1093/gbe/evr067pubmed: 21803766google scholar: lookup
      6. Iwańczyk E, Juras R, Cholewiński G, Cothran EG. Genetic structure and phylogenetic relationships of the Polish Heavy horse. J Appl Genet 2006;47(4):353-9.
        doi: 10.1007/BF03194645pubmed: 17132900google scholar: lookup
      7. Hedrick PW, Parker KM, Miller EL, Miller PS. Major histocompatibility complex variation in the endangered Przewalski's horse. Genetics 1999 Aug;152(4):1701-10.
        doi: 10.1093/genetics/152.4.1701pubmed: 10430594google scholar: lookup