Analyze Diet
Animal genetics2019; 50(4); 347-357; doi: 10.1111/age.12798

A genomic prediction model for racecourse starts in the Thoroughbred horse.

Abstract: Durability traits in Thoroughbred horses are heritable, economically valuable and may affect horse welfare. The aims of this study were to test the hypotheses that (i) durability traits are heritable and (ii) genetic data may be used to predict a horse's potential to have a racecourse start. Heritability for the phenotype 'number of 2- and 3-year-old starts' was estimated to be  = 0.11 ± 0.02 (n = 4499). A genome-wide association study identified SNP contributions to the trait. The neurotrimin (NTM), opioid-binding protein/cell adhesion molecule like (OPCML) and prolylcarboxypeptidase (PRCP) genes were identified as candidate genes associated with the trait. NTM functions in brain development and has been shown to have been selected during the domestication of the horse. PRCP is an established expression quantitative trait locus involved in the interaction between voluntary exercise and body composition in mice. We hypothesise that variation at these loci contributes to the motivation of the horse to exercise, which may influence its response to the demands of the training and racing environment. A random forest with mixed effects (RFME) model identified a set of SNPs that contributed to 24.7% of the heritable variation in the trait. In an independent validation set (n = 528 horses), the cohort with high genetic potential for a racecourse start had significantly fewer unraced horses (16% unraced) than did low (27% unraced) potential horses and had more favourable race outcomes among those that raced. Therefore, the information from SNPs included in the model may be used to predict horses with a greater chance of a racecourse start.
Publication Date: 2019-07-01 PubMed ID: 31257665DOI: 10.1111/age.12798Google 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 research paper discusses the development of a genetic prediction model to ascertain the potential for Thoroughbred horses to start in races. The study proves the hypothesis that traits of durability are inheritable while also exploring specific genes associated with this trait.

Heritability of Durability Traits

  • The research group put forward two hypotheses: durability traits in Thoroughbred horses are heritable and genetic data could predict a horse’s potential to start a race.
  • ‘Number of 2- and 3-year-old starts’ was selected as the phenotype; the heritability of this characteristic was measured and found to be 0.11 ± 0.02, indicating notable inherited traits. This was based on data from 4,499 horses.

Genomewide Association Study

  • The researchers conducted a genome-wide association study to determine which Single Nucleotide Polymorphisms (SNPs) contributed to the trait.
  • The study identified certain genes associated with the trait – the neurotrimin (NTM), opioid-binding protein/cell adhesion molecule like (OPCML), and prolylcarboxypeptidase (PRCP).
  • NTM is involved in brain development and was shown to have an influential role during the domestication of the horse.
  • PRCP has been identified experimentally as an expression quantitative trait locus that mediates the interaction between voluntary exercise and body composition in mice.
  • The researchers proposed that the variation in these genes contributes to a horse’s motivation to exercise, affecting their response to training and racing.

Development and Validation of Prediction Model

  • The research team designed a Random Forest with Mixed Effects (RFME) model, identifying a set of SNPs that contributed to 24.7% of the heritable variation in the trait.
  • The model was validated using an independent validation set consisting of 528 horses.
  • Data analysis revealed that groups with a high genetic potential for racing had a significantly smaller percentage of unraced horses (16%) as compared to groups with a low genetic potential for racing (27%).
  • Additionally, the group with a high genetic potential for racing demonstrated better racing outcomes than the lower potential group amongst those that raced.
  • The research thus concludes that the information from the SNPs included in the model can be used to predict the horses with a greater chance of starting at a racecourse effectively.

Cite This Article

APA
McGivney BA, Hernandez B, Katz LM, MacHugh DE, McGovern SP, Parnell AC, Wiencko HL, Hill EW. (2019). A genomic prediction model for racecourse starts in the Thoroughbred horse. Anim Genet, 50(4), 347-357. https://doi.org/10.1111/age.12798

Publication

ISSN: 1365-2052
NlmUniqueID: 8605704
Country: England
Language: English
Volume: 50
Issue: 4
Pages: 347-357

Researcher Affiliations

McGivney, B A
  • Plusvital Ltd, The Highline, Dun Laoghaire Industrial Estate, Dun Laoghaire, Dublin, Ireland.
Hernandez, B
  • Prolego Scientific, Nova UCD, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
  • The Irish Longitudinal Study on Aging (TILDA), Trinity College Dublin, Dublin, D02 PN40, Ireland.
Katz, L M
  • UCD School of Veterinary Medicine, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
MacHugh, D E
  • UCD Conway Institute for Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
  • UCD School of Agriculture and Food Science, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
McGovern, S P
  • Plusvital Ltd, The Highline, Dun Laoghaire Industrial Estate, Dun Laoghaire, Dublin, Ireland.
Parnell, A C
  • Prolego Scientific, Nova UCD, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
  • School of Mathematics and Statistics, Insight Centre for Data Analytics, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.
Wiencko, H L
  • Plusvital Ltd, The Highline, Dun Laoghaire Industrial Estate, Dun Laoghaire, Dublin, Ireland.
Hill, E W
  • Plusvital Ltd, The Highline, Dun Laoghaire Industrial Estate, Dun Laoghaire, Dublin, Ireland.
  • UCD School of Agriculture and Food Science, University College Dublin, Belfield, Dublin, D04 V1W8, Ireland.

MeSH Terms

  • Animals
  • Genome-Wide Association Study
  • Horses / genetics
  • Horses / physiology
  • Models, Biological
  • Phenotype
  • Physical Conditioning, Animal
  • Polymorphism, Single Nucleotide

Grant Funding

  • Plusvital Ltd.

Citations

This article has been cited 7 times.
  1. Dementieva N, Nikitkina E, Shcherbakov Y, Nikolaeva O, Mitrofanova O, Ryabova A, Atroshchenko M, Makhmutova O, Zaitsev A. The Genetic Diversity of Stallions of Different Breeds in Russia.. Genes (Basel) 2023 Jul 24;14(7).
    doi: 10.3390/genes14071511pubmed: 37510415google scholar: lookup
  2. Xing J, Qi X, Liu G, Li X, Gao X, Bou G, Bai D, Zhao Y, Du M, Dugarjaviin M, Zhang X. A Transcriptomic Regulatory Network among miRNAs, lncRNAs, circRNAs, and mRNAs Associated with L-leucine-induced Proliferation of Equine Satellite Cells.. Animals (Basel) 2023 Jan 6;13(2).
    doi: 10.3390/ani13020208pubmed: 36670748google scholar: lookup
  3. Kim YM, Ha SJ, Seong HS, Choi JY, Baek HJ, Yang BC, Choi JW, Kim NY. Identification of Copy Number Variations in Four Horse Breed Populations in South Korea.. Animals (Basel) 2022 Dec 12;12(24).
    doi: 10.3390/ani12243501pubmed: 36552421google scholar: lookup
  4. Han H, McGivney BA, Allen L, Bai D, Corduff LR, Davaakhuu G, Davaasambuu J, Dorjgotov D, Hall TJ, Hemmings AJ, Holtby AR, Jambal T, Jargalsaikhan B, Jargalsaikhan U, Kadri NK, MacHugh DE, Pausch H, Readhead C, Warburton D, Dugarjaviin M, Hill EW. Common protein-coding variants influence the racing phenotype in galloping racehorse breeds.. Commun Biol 2022 Dec 13;5(1):1320.
    doi: 10.1038/s42003-022-04206-xpubmed: 36513809google scholar: lookup
  5. Littiere TO, Castro GHF, Rodriguez MDPR, Bonafé CM, Magalhães AFB, Faleiros RR, Vieira JIG, Santos CG, Verardo LL. Identification and Functional Annotation of Genes Related to Horses' Performance: From GWAS to Post-GWAS.. Animals (Basel) 2020 Jul 10;10(7).
    doi: 10.3390/ani10071173pubmed: 32664293google scholar: lookup
  6. Han H, McGivney BA, Farries G, Katz LM, MacHugh DE, Randhawa IAS, Hill EW. Selection in Australian Thoroughbred horses acts on a locus associated with early two-year old speed.. PLoS One 2020;15(2):e0227212.
    doi: 10.1371/journal.pone.0227212pubmed: 32049967google scholar: lookup
  7. McGivney BA, Han H, Corduff LR, Katz LM, Tozaki T, MacHugh DE, Hill EW. Genomic inbreeding trends, influential sire lines and selection in the global Thoroughbred horse population.. Sci Rep 2020 Jan 16;10(1):466.
    doi: 10.1038/s41598-019-57389-5pubmed: 31949252google scholar: lookup