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Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution

Skeletal muscle fibers express distinct gene programs during development and maturation, but the underlying gene regulatory networks that confer stage-specific myofiber properties remain unknown. To decipher these distinctive gene programs and how they respond to neural activity, we generated a comb...

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Autores principales: Dos Santos, Matthieu, Shah, Akansha M., Zhang, Yichi, Bezprozvannaya, Svetlana, Chen, Kenian, Xu, Lin, Lin, Weichun, McAnally, John R., Bassel-Duby, Rhonda, Liu, Ning, Olson, Eric N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356771/
https://www.ncbi.nlm.nih.gov/pubmed/37468485
http://dx.doi.org/10.1038/s41467-023-40073-8
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author Dos Santos, Matthieu
Shah, Akansha M.
Zhang, Yichi
Bezprozvannaya, Svetlana
Chen, Kenian
Xu, Lin
Lin, Weichun
McAnally, John R.
Bassel-Duby, Rhonda
Liu, Ning
Olson, Eric N.
author_facet Dos Santos, Matthieu
Shah, Akansha M.
Zhang, Yichi
Bezprozvannaya, Svetlana
Chen, Kenian
Xu, Lin
Lin, Weichun
McAnally, John R.
Bassel-Duby, Rhonda
Liu, Ning
Olson, Eric N.
author_sort Dos Santos, Matthieu
collection PubMed
description Skeletal muscle fibers express distinct gene programs during development and maturation, but the underlying gene regulatory networks that confer stage-specific myofiber properties remain unknown. To decipher these distinctive gene programs and how they respond to neural activity, we generated a combined multi-omic single-nucleus RNA-seq and ATAC-seq atlas of mouse skeletal muscle development at multiple stages of embryonic, fetal, and postnatal life. We found that Myogenin, Klf5, and Tead4 form a transcriptional complex that synergistically activates the expression of muscle genes in developing myofibers. During myofiber maturation, the transcription factor Maf acts as a transcriptional switch to activate the mature fast muscle gene program. In skeletal muscles of mutant mice lacking voltage-gated L-type Ca(2+) channels (Cav1.1), Maf expression and myofiber maturation are impaired. These findings provide a transcriptional atlas of muscle development and reveal genetic links between myofiber formation, maturation, and contraction.
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spelling pubmed-103567712023-07-21 Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution Dos Santos, Matthieu Shah, Akansha M. Zhang, Yichi Bezprozvannaya, Svetlana Chen, Kenian Xu, Lin Lin, Weichun McAnally, John R. Bassel-Duby, Rhonda Liu, Ning Olson, Eric N. Nat Commun Article Skeletal muscle fibers express distinct gene programs during development and maturation, but the underlying gene regulatory networks that confer stage-specific myofiber properties remain unknown. To decipher these distinctive gene programs and how they respond to neural activity, we generated a combined multi-omic single-nucleus RNA-seq and ATAC-seq atlas of mouse skeletal muscle development at multiple stages of embryonic, fetal, and postnatal life. We found that Myogenin, Klf5, and Tead4 form a transcriptional complex that synergistically activates the expression of muscle genes in developing myofibers. During myofiber maturation, the transcription factor Maf acts as a transcriptional switch to activate the mature fast muscle gene program. In skeletal muscles of mutant mice lacking voltage-gated L-type Ca(2+) channels (Cav1.1), Maf expression and myofiber maturation are impaired. These findings provide a transcriptional atlas of muscle development and reveal genetic links between myofiber formation, maturation, and contraction. Nature Publishing Group UK 2023-07-19 /pmc/articles/PMC10356771/ /pubmed/37468485 http://dx.doi.org/10.1038/s41467-023-40073-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Dos Santos, Matthieu
Shah, Akansha M.
Zhang, Yichi
Bezprozvannaya, Svetlana
Chen, Kenian
Xu, Lin
Lin, Weichun
McAnally, John R.
Bassel-Duby, Rhonda
Liu, Ning
Olson, Eric N.
Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title_full Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title_fullStr Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title_full_unstemmed Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title_short Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
title_sort opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356771/
https://www.ncbi.nlm.nih.gov/pubmed/37468485
http://dx.doi.org/10.1038/s41467-023-40073-8
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