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Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse
Variation in the myostatin (MSTN) gene has been reported to be associated with race distance, body composition and skeletal muscle fibre composition in the horse. The aim of the present study was to test the hypothesis that MSTN variation influences mitochondrial phenotypes in equine skeletal muscle...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708611/ https://www.ncbi.nlm.nih.gov/pubmed/29190290 http://dx.doi.org/10.1371/journal.pone.0186247 |
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author | Rooney, Mary F. Porter, Richard K. Katz, Lisa M. Hill, Emmeline W. |
author_facet | Rooney, Mary F. Porter, Richard K. Katz, Lisa M. Hill, Emmeline W. |
author_sort | Rooney, Mary F. |
collection | PubMed |
description | Variation in the myostatin (MSTN) gene has been reported to be associated with race distance, body composition and skeletal muscle fibre composition in the horse. The aim of the present study was to test the hypothesis that MSTN variation influences mitochondrial phenotypes in equine skeletal muscle. Mitochondrial abundance and skeletal muscle fibre types were measured in whole muscle biopsies from the gluteus medius of n = 82 untrained (21 ± 3 months) Thoroughbred horses. Skeletal muscle fibre type proportions were significantly (p < 0.01) different among the three MSTN genotypes and mitochondrial content was significantly (p < 0.01) lower in the combined presence of the C-allele of SNP g.66493737C>T (C) and the SINE insertion 227 bp polymorphism (I). Evaluation of mitochondrial complex activities indicated higher combined mitochondrial complex I+III and II+III activities in the presence of the C-allele / I allele (p ≤ 0.05). The restoration of complex I+III and complex II+III activities following addition of exogenous coenzyme Q(1) (ubiquinone(1)) (CoQ(1)) in vitro in the TT/NN (homozygous T allele/homozygous no insertion) cohort indicated decreased coenzyme Q in these animals. In addition, decreased gene expression in two coenzyme Q (CoQ) biosynthesis pathway genes (COQ4, p ≤ 0.05; ADCK3, p ≤ 0.01) in the TT/NN horses was observed. This study has identified several mitochondrial phenotypes associated with MSTN genotype in untrained Thoroughbred horses and in addition, our findings suggest that nutritional supplementation with CoQ may aid to restore coenzyme Q activity in TT/NN horses. |
format | Online Article Text |
id | pubmed-5708611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57086112017-12-15 Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse Rooney, Mary F. Porter, Richard K. Katz, Lisa M. Hill, Emmeline W. PLoS One Research Article Variation in the myostatin (MSTN) gene has been reported to be associated with race distance, body composition and skeletal muscle fibre composition in the horse. The aim of the present study was to test the hypothesis that MSTN variation influences mitochondrial phenotypes in equine skeletal muscle. Mitochondrial abundance and skeletal muscle fibre types were measured in whole muscle biopsies from the gluteus medius of n = 82 untrained (21 ± 3 months) Thoroughbred horses. Skeletal muscle fibre type proportions were significantly (p < 0.01) different among the three MSTN genotypes and mitochondrial content was significantly (p < 0.01) lower in the combined presence of the C-allele of SNP g.66493737C>T (C) and the SINE insertion 227 bp polymorphism (I). Evaluation of mitochondrial complex activities indicated higher combined mitochondrial complex I+III and II+III activities in the presence of the C-allele / I allele (p ≤ 0.05). The restoration of complex I+III and complex II+III activities following addition of exogenous coenzyme Q(1) (ubiquinone(1)) (CoQ(1)) in vitro in the TT/NN (homozygous T allele/homozygous no insertion) cohort indicated decreased coenzyme Q in these animals. In addition, decreased gene expression in two coenzyme Q (CoQ) biosynthesis pathway genes (COQ4, p ≤ 0.05; ADCK3, p ≤ 0.01) in the TT/NN horses was observed. This study has identified several mitochondrial phenotypes associated with MSTN genotype in untrained Thoroughbred horses and in addition, our findings suggest that nutritional supplementation with CoQ may aid to restore coenzyme Q activity in TT/NN horses. Public Library of Science 2017-11-30 /pmc/articles/PMC5708611/ /pubmed/29190290 http://dx.doi.org/10.1371/journal.pone.0186247 Text en © 2017 Rooney et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Rooney, Mary F. Porter, Richard K. Katz, Lisa M. Hill, Emmeline W. Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title | Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title_full | Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title_fullStr | Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title_full_unstemmed | Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title_short | Skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the Thoroughbred horse |
title_sort | skeletal muscle mitochondrial bioenergetics and associations with myostatin genotypes in the thoroughbred horse |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708611/ https://www.ncbi.nlm.nih.gov/pubmed/29190290 http://dx.doi.org/10.1371/journal.pone.0186247 |
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