Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.

The ovine Callipyge mutation causes postnatal muscle hypertrophy localized to the pelvic limbs and torso, as well as body leanness. The mechanism underpinning enhanced muscle mass is unclear, as is the systemic impact of the mutation. Using muscle fibre typing immunohistochemistry, we confirmed musc...

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Main Authors: Juan Li, Paul L Greenwood, Noelle E Cockett, Tracy S Hadfield, Tony Vuocolo, Keren Byrne, Jason D White, Ross L Tellam, Horst Joachim Schirra
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4061035?pdf=render
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spelling doaj-833ae95d0f2c4c22b221489626d8b5062020-11-25T01:26:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0196e9972610.1371/journal.pone.0099726Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.Juan LiPaul L GreenwoodNoelle E CockettTracy S HadfieldTony VuocoloKeren ByrneJason D WhiteRoss L TellamHorst Joachim SchirraThe ovine Callipyge mutation causes postnatal muscle hypertrophy localized to the pelvic limbs and torso, as well as body leanness. The mechanism underpinning enhanced muscle mass is unclear, as is the systemic impact of the mutation. Using muscle fibre typing immunohistochemistry, we confirmed muscle specific effects and demonstrated that affected muscles had greater prevalence and hypertrophy of type 2X fast twitch glycolytic fibres and decreased representation of types 1, 2C, 2A and/or 2AX fibres. To investigate potential systemic effects of the mutation, proton NMR spectra of plasma taken from lambs at 8 and 12 weeks of age were measured. Multivariate statistical analysis of plasma metabolite profiles demonstrated effects of development and genotype but not gender. Plasma from Callipyge lambs at 12 weeks of age, but not 8 weeks, was characterized by a metabolic profile consistent with contributions from the affected hypertrophic fast twitch glycolytic muscle fibres. Microarray analysis of the perirenal adipose tissue depot did not reveal a transcriptional effect of the mutation in this tissue. We conclude that there is an indirect systemic effect of the Callipyge mutation in skeletal muscle in the form of changes of blood metabolites, which may contribute to secondary phenotypes such as body leanness.http://europepmc.org/articles/PMC4061035?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Juan Li
Paul L Greenwood
Noelle E Cockett
Tracy S Hadfield
Tony Vuocolo
Keren Byrne
Jason D White
Ross L Tellam
Horst Joachim Schirra
spellingShingle Juan Li
Paul L Greenwood
Noelle E Cockett
Tracy S Hadfield
Tony Vuocolo
Keren Byrne
Jason D White
Ross L Tellam
Horst Joachim Schirra
Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
PLoS ONE
author_facet Juan Li
Paul L Greenwood
Noelle E Cockett
Tracy S Hadfield
Tony Vuocolo
Keren Byrne
Jason D White
Ross L Tellam
Horst Joachim Schirra
author_sort Juan Li
title Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
title_short Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
title_full Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
title_fullStr Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
title_full_unstemmed Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
title_sort impacts of the callipyge mutation on ovine plasma metabolites and muscle fibre type.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description The ovine Callipyge mutation causes postnatal muscle hypertrophy localized to the pelvic limbs and torso, as well as body leanness. The mechanism underpinning enhanced muscle mass is unclear, as is the systemic impact of the mutation. Using muscle fibre typing immunohistochemistry, we confirmed muscle specific effects and demonstrated that affected muscles had greater prevalence and hypertrophy of type 2X fast twitch glycolytic fibres and decreased representation of types 1, 2C, 2A and/or 2AX fibres. To investigate potential systemic effects of the mutation, proton NMR spectra of plasma taken from lambs at 8 and 12 weeks of age were measured. Multivariate statistical analysis of plasma metabolite profiles demonstrated effects of development and genotype but not gender. Plasma from Callipyge lambs at 12 weeks of age, but not 8 weeks, was characterized by a metabolic profile consistent with contributions from the affected hypertrophic fast twitch glycolytic muscle fibres. Microarray analysis of the perirenal adipose tissue depot did not reveal a transcriptional effect of the mutation in this tissue. We conclude that there is an indirect systemic effect of the Callipyge mutation in skeletal muscle in the form of changes of blood metabolites, which may contribute to secondary phenotypes such as body leanness.
url http://europepmc.org/articles/PMC4061035?pdf=render
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