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Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism

Skeletal muscle is composed of both slow-twitch oxidative myofibers and fast-twitch glycolytic myofibers that differentially impact muscle metabolism, function and eventually whole-body physiology. Here we show that the mesodermal transcription factor T-box 15 (Tbx15) is highly and specifically expr...

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Autores principales: Lee, Kevin Y., Singh, Manvendra K., Ussar, Siegfried, Wetzel, Petra, Hirshman, Michael F., Goodyear, Laurie J., Kispert, Andreas, Kahn, C. Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552045/
https://www.ncbi.nlm.nih.gov/pubmed/26299309
http://dx.doi.org/10.1038/ncomms9054
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author Lee, Kevin Y.
Singh, Manvendra K.
Ussar, Siegfried
Wetzel, Petra
Hirshman, Michael F.
Goodyear, Laurie J.
Kispert, Andreas
Kahn, C. Ronald
author_facet Lee, Kevin Y.
Singh, Manvendra K.
Ussar, Siegfried
Wetzel, Petra
Hirshman, Michael F.
Goodyear, Laurie J.
Kispert, Andreas
Kahn, C. Ronald
author_sort Lee, Kevin Y.
collection PubMed
description Skeletal muscle is composed of both slow-twitch oxidative myofibers and fast-twitch glycolytic myofibers that differentially impact muscle metabolism, function and eventually whole-body physiology. Here we show that the mesodermal transcription factor T-box 15 (Tbx15) is highly and specifically expressed in glycolytic myofibers. Ablation of Tbx15 in vivo leads to a decrease in muscle size due to a decrease in the number of glycolytic fibres, associated with a small increase in the number of oxidative fibres. This shift in fibre composition results in muscles with slower myofiber contraction and relaxation, and also decreases whole-body oxygen consumption, reduces spontaneous activity, increases adiposity and glucose intolerance. Mechanistically, ablation of Tbx15 leads to activation of AMPK signalling and a decrease in Igf2 expression. Thus, Tbx15 is one of a limited number of transcription factors to be identified with a critical role in regulating glycolytic fibre identity and muscle metabolism.
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spelling pubmed-45520452015-09-14 Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism Lee, Kevin Y. Singh, Manvendra K. Ussar, Siegfried Wetzel, Petra Hirshman, Michael F. Goodyear, Laurie J. Kispert, Andreas Kahn, C. Ronald Nat Commun Article Skeletal muscle is composed of both slow-twitch oxidative myofibers and fast-twitch glycolytic myofibers that differentially impact muscle metabolism, function and eventually whole-body physiology. Here we show that the mesodermal transcription factor T-box 15 (Tbx15) is highly and specifically expressed in glycolytic myofibers. Ablation of Tbx15 in vivo leads to a decrease in muscle size due to a decrease in the number of glycolytic fibres, associated with a small increase in the number of oxidative fibres. This shift in fibre composition results in muscles with slower myofiber contraction and relaxation, and also decreases whole-body oxygen consumption, reduces spontaneous activity, increases adiposity and glucose intolerance. Mechanistically, ablation of Tbx15 leads to activation of AMPK signalling and a decrease in Igf2 expression. Thus, Tbx15 is one of a limited number of transcription factors to be identified with a critical role in regulating glycolytic fibre identity and muscle metabolism. Nature Pub. Group 2015-08-24 /pmc/articles/PMC4552045/ /pubmed/26299309 http://dx.doi.org/10.1038/ncomms9054 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Kevin Y.
Singh, Manvendra K.
Ussar, Siegfried
Wetzel, Petra
Hirshman, Michael F.
Goodyear, Laurie J.
Kispert, Andreas
Kahn, C. Ronald
Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title_full Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title_fullStr Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title_full_unstemmed Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title_short Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
title_sort tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552045/
https://www.ncbi.nlm.nih.gov/pubmed/26299309
http://dx.doi.org/10.1038/ncomms9054
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