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Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration

Fundamental aspects underlying downstream processes of skeletal muscle regeneration, such as myonuclear positioning and transcription are poorly understood. This investigation begins to address deficiencies in knowledge by examining the kinetics of myonuclear accretion, positioning, and global trans...

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Autores principales: Buckley, Kole H., Nestor-Kalinoski, Andrea L., Pizza, Francis X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040890/
https://www.ncbi.nlm.nih.gov/pubmed/35492593
http://dx.doi.org/10.3389/fphys.2022.845504
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author Buckley, Kole H.
Nestor-Kalinoski, Andrea L.
Pizza, Francis X.
author_facet Buckley, Kole H.
Nestor-Kalinoski, Andrea L.
Pizza, Francis X.
author_sort Buckley, Kole H.
collection PubMed
description Fundamental aspects underlying downstream processes of skeletal muscle regeneration, such as myonuclear positioning and transcription are poorly understood. This investigation begins to address deficiencies in knowledge by examining the kinetics of myonuclear accretion, positioning, and global transcription during injury-induced muscle regeneration in mice. We demonstrate that myonuclear accretion plateaus within 7 days of an injury and that the majority (∼70%) of myonuclei are centrally aligned in linear arrays (nuclear chains) throughout the course of regeneration. Relatively few myonuclei were found in a peripheral position (∼20%) or clustered (∼10%) together during regeneration. Importantly, transcriptional activity of individual myonuclei in nuclear chains was high, and greater than that of peripheral or clustered myonuclei. Transcription occurring primarily in nuclear chains elevated the collective transcriptional activity of regenerating myofibers during the later stage of regeneration. Importantly, the number of myonuclei in chains and their transcriptional activity were statistically correlated with an increase in myofiber size during regeneration. Our findings demonstrate the positional context of transcription during regeneration and highlight the importance of centralized nuclear chains in facilitating hypertrophy of regenerating myofibers after injury.
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spelling pubmed-90408902022-04-27 Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration Buckley, Kole H. Nestor-Kalinoski, Andrea L. Pizza, Francis X. Front Physiol Physiology Fundamental aspects underlying downstream processes of skeletal muscle regeneration, such as myonuclear positioning and transcription are poorly understood. This investigation begins to address deficiencies in knowledge by examining the kinetics of myonuclear accretion, positioning, and global transcription during injury-induced muscle regeneration in mice. We demonstrate that myonuclear accretion plateaus within 7 days of an injury and that the majority (∼70%) of myonuclei are centrally aligned in linear arrays (nuclear chains) throughout the course of regeneration. Relatively few myonuclei were found in a peripheral position (∼20%) or clustered (∼10%) together during regeneration. Importantly, transcriptional activity of individual myonuclei in nuclear chains was high, and greater than that of peripheral or clustered myonuclei. Transcription occurring primarily in nuclear chains elevated the collective transcriptional activity of regenerating myofibers during the later stage of regeneration. Importantly, the number of myonuclei in chains and their transcriptional activity were statistically correlated with an increase in myofiber size during regeneration. Our findings demonstrate the positional context of transcription during regeneration and highlight the importance of centralized nuclear chains in facilitating hypertrophy of regenerating myofibers after injury. Frontiers Media S.A. 2022-03-23 /pmc/articles/PMC9040890/ /pubmed/35492593 http://dx.doi.org/10.3389/fphys.2022.845504 Text en Copyright © 2022 Buckley, Nestor-Kalinoski and Pizza. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Buckley, Kole H.
Nestor-Kalinoski, Andrea L.
Pizza, Francis X.
Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title_full Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title_fullStr Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title_full_unstemmed Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title_short Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
title_sort positional context of myonuclear transcription during injury-induced muscle regeneration
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040890/
https://www.ncbi.nlm.nih.gov/pubmed/35492593
http://dx.doi.org/10.3389/fphys.2022.845504
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