Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis

Growth and maintenance of skeletal muscle fibres depend on coordinated activation and return to quiescence of resident muscle stem cells (MuSCs). The transcription factor Myogenin (Myog) regulates myocyte fusion during development, but its role in adult myogenesis remains unclear. In contrast to mic...

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Main Authors: Massimo Ganassi, Sara Badodi, Kees Wanders, Peter S Zammit, Simon M Hughes
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-10-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/60445
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spelling doaj-c87413b34e054660a1d96d15fa15daa22021-05-05T21:34:21ZengeLife Sciences Publications LtdeLife2050-084X2020-10-01910.7554/eLife.60445Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasisMassimo Ganassi0https://orcid.org/0000-0003-3163-9707Sara Badodi1https://orcid.org/0000-0002-8407-8336Kees Wanders2https://orcid.org/0000-0003-3209-9853Peter S Zammit3https://orcid.org/0000-0001-9562-3072Simon M Hughes4https://orcid.org/0000-0001-8227-9225Randall Centre for Cell and Molecular Biophysics, King’s College London, London, United KingdomBlizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United KingdomRandall Centre for Cell and Molecular Biophysics, King’s College London, London, United KingdomRandall Centre for Cell and Molecular Biophysics, King’s College London, London, United KingdomRandall Centre for Cell and Molecular Biophysics, King’s College London, London, United KingdomGrowth and maintenance of skeletal muscle fibres depend on coordinated activation and return to quiescence of resident muscle stem cells (MuSCs). The transcription factor Myogenin (Myog) regulates myocyte fusion during development, but its role in adult myogenesis remains unclear. In contrast to mice, myog-/-zebrafish are viable, but have hypotrophic muscles. By isolating adult myofibres with associated MuSCs, we found that myog-/- myofibres have severely reduced nuclear number, but increased myonuclear domain size. Expression of fusogenic genes is decreased, Pax7 upregulated, MuSCs are fivefold more numerous and mis-positioned throughout the length of myog-/-myofibres instead of localising at myofibre ends as in wild-type. Loss of Myog dysregulates mTORC1 signalling, resulting in an ‘alerted’ state of MuSCs, which display precocious activation and faster cell cycle entry ex vivo, concomitant with myod upregulation. Thus, beyond controlling myocyte fusion, Myog influences the MuSC:niche relationship, demonstrating a multi-level contribution to muscle homeostasis throughout life.https://elifesciences.org/articles/60445muscle fiberstem cellmyogenincell sizenicheadult
collection DOAJ
language English
format Article
sources DOAJ
author Massimo Ganassi
Sara Badodi
Kees Wanders
Peter S Zammit
Simon M Hughes
spellingShingle Massimo Ganassi
Sara Badodi
Kees Wanders
Peter S Zammit
Simon M Hughes
Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
eLife
muscle fiber
stem cell
myogenin
cell size
niche
adult
author_facet Massimo Ganassi
Sara Badodi
Kees Wanders
Peter S Zammit
Simon M Hughes
author_sort Massimo Ganassi
title Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
title_short Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
title_full Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
title_fullStr Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
title_full_unstemmed Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
title_sort myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-10-01
description Growth and maintenance of skeletal muscle fibres depend on coordinated activation and return to quiescence of resident muscle stem cells (MuSCs). The transcription factor Myogenin (Myog) regulates myocyte fusion during development, but its role in adult myogenesis remains unclear. In contrast to mice, myog-/-zebrafish are viable, but have hypotrophic muscles. By isolating adult myofibres with associated MuSCs, we found that myog-/- myofibres have severely reduced nuclear number, but increased myonuclear domain size. Expression of fusogenic genes is decreased, Pax7 upregulated, MuSCs are fivefold more numerous and mis-positioned throughout the length of myog-/-myofibres instead of localising at myofibre ends as in wild-type. Loss of Myog dysregulates mTORC1 signalling, resulting in an ‘alerted’ state of MuSCs, which display precocious activation and faster cell cycle entry ex vivo, concomitant with myod upregulation. Thus, beyond controlling myocyte fusion, Myog influences the MuSC:niche relationship, demonstrating a multi-level contribution to muscle homeostasis throughout life.
topic muscle fiber
stem cell
myogenin
cell size
niche
adult
url https://elifesciences.org/articles/60445
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