Evidence map›Paper›PMID 31136578›Full record

ArticlePLoS genetics2019

Identification and validation of genetic variants predictive of gait in standardbred horses.

Annette M McCoy, Samantha K Beeson, Carl-Johan Rubin, Leif Andersson, Paul Caputo, Sigrid Lykkjen, Alison Moore, Richard J Piercy, James R Mickelson, Molly E McCue

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.5field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Genomic analysis of gaits and racing performance of the French trotter.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2021
    Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 4 countries.

Annette M McCoyDepartment of Veterinary Clinical Medicine, University of Illinois, Urbana, Illinois, United States of America.ORCID 0000-0003-4088-6902
Samantha K BeesonVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota, United States of America.
Carl-Johan RubinDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Leif AnderssonDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-4085-6968
Paul CaputoPaul Caputo, DVM, Pompano Beach, Florida, United States of America.
Sigrid LykkjenFaculty of Veterinary Medicine, Norwegian University of Life Sciences, Oslo, Norway.ORCID 0000-0001-8017-1261
Alison MooreMoore Equine Services, Cambridge, Ontario, Canada.
Richard J PiercyDepartment of Clinical Sciences and Services, Royal Veterinary College, London, United Kingdom.ORCID 0000-0002-4344-6438
James R MickelsonVeterinary and Biomedical Sciences Department, University of Minnesota, St. Paul, Minnesota, United States of America.ORCID 0000-0001-6951-0234
Molly E McCueVeterinary Population Medicine Department, University of Minnesota, St. Paul, Minnesota, United States of America.ORCID 0000-0002-6807-0318
University of Minnesota · USUppsala University · SENorwegian University of Life Sciences · NORoyal Veterinary College · GBUniversity of Illinois Urbana-Champaign · US

Funding

Comparative Medicine and Pathology TrainingT32OD010993 · OD · UNIVERSITY OF MINNESOTA · PI DAVID R BROWN, Cathy S. Carlson · 2012 to 2026
$6.2M
Regulation of Glycogen Metabolism: Insights from Novel Genetic ModelsK08AR055713 · NIAMS · UNIVERSITY OF MINNESOTA · PI MCCUE, MOLLY E · 2009 to 2013
$644k
Genetic bases of exercise induced rhabdomyolysisF30OD023369 · OD · UNIVERSITY OF MINNESOTA · PI BEESON, SAMANTHA K · 2017 to 2020
$181k
NIAMS NIH HHS K08 AR055713NIH HHS F30 OD023369NIH HHS T32 OD010993
6 · The paper itself

Abstract

Several horse breeds have been specifically selected for the ability to exhibit alternative patterns of locomotion, or gaits. A premature stop codon in the gene DMRT3 is permissive for "gaitedness" across breeds. However, this mutation is nearly fixed in both American Standardbred trotters and pacers, which perform a diagonal and lateral gait, respectively, during harness racing. This suggests that modifying alleles must influence the preferred gait at racing speeds in these populations. A genome-wide association analysis for the ability to pace was performed in 542 Standardbred horses (n = 176 pacers, n = 366 trotters) with genotype data imputed to ~74,000 single nucleotide polymorphisms (SNPs). Nineteen SNPs on nine chromosomes (ECA1, 2, 6, 9, 17, 19, 23, 25, 31) reached genome-wide significance (p < 1.44 x 10-6). Variant discovery in regions of interest was carried out via whole-genome sequencing. A set of 303 variants from 22 chromosomes with putative modifying effects on gait was genotyped in 659 Standardbreds (n = 231 pacers, n = 428 trotters) using a high-throughput assay. Random forest classification analysis resulted in an out-of-box error rate of 0.61%. A conditional inference tree algorithm containing seven SNPs predicted status as a pacer or trotter with 99.1% accuracy and subsequently performed with 99.4% accuracy in an independently sampled population of 166 Standardbreds (n = 83 pacers, n = 83 trotters). This highly accurate algorithm could be used by owners/trainers to identify Standardbred horses with the potential to race as pacers or as trotters, according to the genotype identified, prior to initiating training and would enable fine-tuning of breeding programs with designed matings. Additional work is needed to determine both the algorithm's utility in other gaited breeds and whether any of the predictive SNPs play a physiologically functional role in the tendency to pace or tag true functional alleles.

Indexed as

AlgorithmsAllelesAnimalsBiomarkersCodon, NonsenseGaitGene FrequencyGenetic VariationGenome-Wide Association StudyGenotypeHorsesLocomotionMutationPolymorphism, Single NucleotideSelective BreedingTranscription FactorsBiomarkersCodon, NonsenseTranscription Factors

Identifiers

PMID31136578
PMCPMC6555539
OpenAlexW2946933911

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.