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Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle
Complex animals build specialised muscles to match specific biomechanical and energetic needs. Hence, composition and architecture of sarcomeres and mitochondria are muscle type specific. However, mechanisms coordinating mitochondria with sarcomere morphogenesis are elusive. Here we use Drosophila m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027795/ https://www.ncbi.nlm.nih.gov/pubmed/33828099 http://dx.doi.org/10.1038/s41467-021-22058-7 |
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author | Avellaneda, Jerome Rodier, Clement Daian, Fabrice Brouilly, Nicolas Rival, Thomas Luis, Nuno Miguel Schnorrer, Frank |
author_facet | Avellaneda, Jerome Rodier, Clement Daian, Fabrice Brouilly, Nicolas Rival, Thomas Luis, Nuno Miguel Schnorrer, Frank |
author_sort | Avellaneda, Jerome |
collection | PubMed |
description | Complex animals build specialised muscles to match specific biomechanical and energetic needs. Hence, composition and architecture of sarcomeres and mitochondria are muscle type specific. However, mechanisms coordinating mitochondria with sarcomere morphogenesis are elusive. Here we use Drosophila muscles to demonstrate that myofibril and mitochondria morphogenesis are intimately linked. In flight muscles, the muscle selector spalt instructs mitochondria to intercalate between myofibrils, which in turn mechanically constrain mitochondria into elongated shapes. Conversely in cross-striated leg muscles, mitochondria networks surround myofibril bundles, contacting myofibrils only with thin extensions. To investigate the mechanism causing these differences, we manipulated mitochondrial dynamics and found that increased mitochondrial fusion during myofibril assembly prevents mitochondrial intercalation in flight muscles. Strikingly, this causes the expression of cross-striated muscle specific sarcomeric proteins. Consequently, flight muscle myofibrils convert towards a partially cross-striated architecture. Together, these data suggest a biomechanical feedback mechanism downstream of spalt synchronizing mitochondria with myofibril morphogenesis. |
format | Online Article Text |
id | pubmed-8027795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80277952021-04-30 Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle Avellaneda, Jerome Rodier, Clement Daian, Fabrice Brouilly, Nicolas Rival, Thomas Luis, Nuno Miguel Schnorrer, Frank Nat Commun Article Complex animals build specialised muscles to match specific biomechanical and energetic needs. Hence, composition and architecture of sarcomeres and mitochondria are muscle type specific. However, mechanisms coordinating mitochondria with sarcomere morphogenesis are elusive. Here we use Drosophila muscles to demonstrate that myofibril and mitochondria morphogenesis are intimately linked. In flight muscles, the muscle selector spalt instructs mitochondria to intercalate between myofibrils, which in turn mechanically constrain mitochondria into elongated shapes. Conversely in cross-striated leg muscles, mitochondria networks surround myofibril bundles, contacting myofibrils only with thin extensions. To investigate the mechanism causing these differences, we manipulated mitochondrial dynamics and found that increased mitochondrial fusion during myofibril assembly prevents mitochondrial intercalation in flight muscles. Strikingly, this causes the expression of cross-striated muscle specific sarcomeric proteins. Consequently, flight muscle myofibrils convert towards a partially cross-striated architecture. Together, these data suggest a biomechanical feedback mechanism downstream of spalt synchronizing mitochondria with myofibril morphogenesis. Nature Publishing Group UK 2021-04-07 /pmc/articles/PMC8027795/ /pubmed/33828099 http://dx.doi.org/10.1038/s41467-021-22058-7 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Avellaneda, Jerome Rodier, Clement Daian, Fabrice Brouilly, Nicolas Rival, Thomas Luis, Nuno Miguel Schnorrer, Frank Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title | Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title_full | Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title_fullStr | Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title_full_unstemmed | Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title_short | Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
title_sort | myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027795/ https://www.ncbi.nlm.nih.gov/pubmed/33828099 http://dx.doi.org/10.1038/s41467-021-22058-7 |
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