Evidence map›Paper›PMID 38678201›Full record

ArticleBMC genomics2024

An autosomal recessive variant in PYGM causes myophosphorylase deficiency in Red Angus composite cattle.

Mackenzie C Batt, Leila G Venzor, Keri Gardner, Rachel R Reith, Kelsey A Roberts, Nicolas J Herrera, Anna M Fuller, Gary A Sullivan, J Travis Mulliniks, Matthew L Spangler and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

13 authors at 2 institutions in 1 country.

Mackenzie C BattDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Leila G VenzorDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Keri GardnerCollege of Veterinary Medicine, Michigan State University, East Lansing, MI, USA.
Rachel R ReithDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Kelsey A RobertsDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Nicolas J HerreraDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Anna M FullerDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Gary A SullivanDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
J Travis MulliniksDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Matthew L SpanglerDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA.
Stephanie J ValbergCollege of Veterinary Medicine, Michigan State University, East Lansing, MI, USA.
David J Steffen *School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE, USA.
Jessica L Petersen *Department of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, USA. jessica.petersen@unl.edu.
University of Nebraska–Lincoln · USMichigan State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBetween 2020 and 2022, eight calves in a Nebraska herd (composite Simmental, Red Angus, Gelbvieh) displayed exercise intolerance during forced activity. In some cases, the calves collapsed and did not recover. Available sire pedigrees contained a paternal ancestor within 2-4 generations in all affected calves. Pedigrees of the calves' dams were unavailable, however, the cows were ranch-raised and retained from prior breeding seasons, where bulls used for breeding occasionally had a common ancestor. Therefore, it was hypothesized that a de novo autosomal recessive variant was causative of exercise intolerance in these calves.

resultsA genome-wide association analysis utilizing SNP data from 6 affected calves and 715 herd mates, followed by whole-genome sequencing of 2 affected calves led to the identification of a variant in the gene PYGM (BTA29:g.42989581G > A). The variant, confirmed to be present in the skeletal muscle transcriptome, was predicted to produce a premature stop codon (p.Arg650*). The protein product of PYGM, myophosphorylase, breaks down glycogen in skeletal muscle. Glycogen concentrations were fluorometrically assayed as glucose residues demonstrating significantly elevated glycogen concentrations in affected calves compared to cattle carrying the variant and to wild-type controls. The absence of the PYGM protein product in skeletal muscle was confirmed by immunohistochemistry and label-free quantitative proteomics analysis; muscle degeneration was confirmed in biopsy and necropsy samples. Elevated skeletal muscle glycogen persisted after harvest, resulting in a high pH and dark-cutting beef, which is negatively perceived by consumers and results in an economic loss to the industry. Carriers of the variant did not exhibit differences in meat quality or any measures of animal well-being.

conclusionsMyophosphorylase deficiency poses welfare concerns for affected animals and negatively impacts the final product. The association of the recessive genotype with dark-cutting beef further demonstrates the importance of genetics to not only animal health but to the quality of their product. Although cattle heterozygous for the variant may not immediately affect the beef industry, identifying carriers will enable selection and breeding strategies to prevent the production of affected calves.

Indexed as

Genome-Wide Association StudyGlycogen Phosphorylase, Muscle FormAnimalsCattleCattle DiseasesFemaleGenes, RecessiveMaleMuscle, SkeletalPedigreePolymorphism, Single NucleotideWhole Genome SequencingGlycogen Phosphorylase, Muscle FormBos taurusDark cutterDe novo variantExercise intoleranceGlycogen storage disease type VLivestock productionMcArdle diseaseMendelian disease

Identifiers

PMID38678201
PMCPMC11055281
OpenAlexW4395703264

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.