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Numb and Numblike regulate sarcomere assembly and maintenance
A sarcomere is the contractile unit of the myofibril in striated muscles such as cardiac and skeletal muscles. The assembly of sarcomeres depends on multiple molecules that serve as raw materials and participate in the assembly process. However, the mechanism of this critical assembly process remain...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803338/ https://www.ncbi.nlm.nih.gov/pubmed/35104799 http://dx.doi.org/10.1172/JCI139420 |
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author | Wang, Baolei Yang, Min Li, Shujuan |
author_facet | Wang, Baolei Yang, Min Li, Shujuan |
author_sort | Wang, Baolei |
collection | PubMed |
description | A sarcomere is the contractile unit of the myofibril in striated muscles such as cardiac and skeletal muscles. The assembly of sarcomeres depends on multiple molecules that serve as raw materials and participate in the assembly process. However, the mechanism of this critical assembly process remains largely unknown. Here, we found that the cell fate determinant Numb and its homolog Numblike regulated sarcomere assembly and maintenance in striated muscles. We discovered that Numb and Numblike are sarcomeric molecules that were gradually confined to the Z-disc during striated muscle development. Conditional knockout of Numb and Numblike severely compromised sarcomere assembly and its integrity and thus caused organelle dysfunction. Notably, we identified that Numb and Numblike served as sarcomeric α-Actin–binding proteins (ABPs) and shared a conserved domain that can bind to the barbed end of sarcomeric α-Actin. In vitro fluorometric α-Actin polymerization assay showed that Numb and Numblike also played a role in the sarcomeric α-Actin polymerization process. Last, we demonstrate that Numb and Numblike regulate sarcomeric α-Actinin–dependent (ACTN-dependent) Z-disc consolidation in the sarcomere assembly and maintenance. In summary, our studies show that Numb and its homolog Numblike regulate sarcomere assembly and maintenance in striated muscles, and demonstrate a molecular mechanism by which Numb/Numblike, sarcomeric α-Actin, and ACTN cooperate to control thin filament formation and Z-disc consolidation. |
format | Online Article Text |
id | pubmed-8803338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-88033382022-02-04 Numb and Numblike regulate sarcomere assembly and maintenance Wang, Baolei Yang, Min Li, Shujuan J Clin Invest Research Article A sarcomere is the contractile unit of the myofibril in striated muscles such as cardiac and skeletal muscles. The assembly of sarcomeres depends on multiple molecules that serve as raw materials and participate in the assembly process. However, the mechanism of this critical assembly process remains largely unknown. Here, we found that the cell fate determinant Numb and its homolog Numblike regulated sarcomere assembly and maintenance in striated muscles. We discovered that Numb and Numblike are sarcomeric molecules that were gradually confined to the Z-disc during striated muscle development. Conditional knockout of Numb and Numblike severely compromised sarcomere assembly and its integrity and thus caused organelle dysfunction. Notably, we identified that Numb and Numblike served as sarcomeric α-Actin–binding proteins (ABPs) and shared a conserved domain that can bind to the barbed end of sarcomeric α-Actin. In vitro fluorometric α-Actin polymerization assay showed that Numb and Numblike also played a role in the sarcomeric α-Actin polymerization process. Last, we demonstrate that Numb and Numblike regulate sarcomeric α-Actinin–dependent (ACTN-dependent) Z-disc consolidation in the sarcomere assembly and maintenance. In summary, our studies show that Numb and its homolog Numblike regulate sarcomere assembly and maintenance in striated muscles, and demonstrate a molecular mechanism by which Numb/Numblike, sarcomeric α-Actin, and ACTN cooperate to control thin filament formation and Z-disc consolidation. American Society for Clinical Investigation 2022-02-01 2022-02-01 /pmc/articles/PMC8803338/ /pubmed/35104799 http://dx.doi.org/10.1172/JCI139420 Text en © 2022 Wang et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Wang, Baolei Yang, Min Li, Shujuan Numb and Numblike regulate sarcomere assembly and maintenance |
title | Numb and Numblike regulate sarcomere assembly and maintenance |
title_full | Numb and Numblike regulate sarcomere assembly and maintenance |
title_fullStr | Numb and Numblike regulate sarcomere assembly and maintenance |
title_full_unstemmed | Numb and Numblike regulate sarcomere assembly and maintenance |
title_short | Numb and Numblike regulate sarcomere assembly and maintenance |
title_sort | numb and numblike regulate sarcomere assembly and maintenance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803338/ https://www.ncbi.nlm.nih.gov/pubmed/35104799 http://dx.doi.org/10.1172/JCI139420 |
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