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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10356771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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