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Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality
Establishing left–right asymmetry is a fundamental process essential for arrangement of visceral organs during development. In vertebrates, motile cilia-driven fluid flow in the left–right organizer (LRO) is essential for initiating symmetry breaking event. Here, we report that myosin 1d (myo1d) is...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107537/ https://www.ncbi.nlm.nih.gov/pubmed/30139971 http://dx.doi.org/10.1038/s41467-018-05866-2 |
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author | Saydmohammed, Manush Yagi, Hisato Calderon, Michael Clark, Madeline J. Feinstein, Timothy Sun, Ming Stolz, Donna B. Watkins, Simon C. Amack, Jeffrey D. Lo, Cecilia W. Tsang, Michael |
author_facet | Saydmohammed, Manush Yagi, Hisato Calderon, Michael Clark, Madeline J. Feinstein, Timothy Sun, Ming Stolz, Donna B. Watkins, Simon C. Amack, Jeffrey D. Lo, Cecilia W. Tsang, Michael |
author_sort | Saydmohammed, Manush |
collection | PubMed |
description | Establishing left–right asymmetry is a fundamental process essential for arrangement of visceral organs during development. In vertebrates, motile cilia-driven fluid flow in the left–right organizer (LRO) is essential for initiating symmetry breaking event. Here, we report that myosin 1d (myo1d) is essential for establishing left–right asymmetry in zebrafish. Using super-resolution microscopy, we show that the zebrafish LRO, Kupffer’s vesicle (KV), fails to form a spherical lumen and establish proper unidirectional flow in the absence of myo1d. This process requires directed vacuolar trafficking in KV epithelial cells. Interestingly, the vacuole transporting function of zebrafish Myo1d can be substituted by myosin1C derived from an ancient eukaryote, Acanthamoeba castellanii, where it regulates the transport of contractile vacuoles. Our findings reveal an evolutionary conserved role for an unconventional myosin in vacuole trafficking, lumen formation, and determining laterality. |
format | Online Article Text |
id | pubmed-6107537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61075372018-08-27 Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality Saydmohammed, Manush Yagi, Hisato Calderon, Michael Clark, Madeline J. Feinstein, Timothy Sun, Ming Stolz, Donna B. Watkins, Simon C. Amack, Jeffrey D. Lo, Cecilia W. Tsang, Michael Nat Commun Article Establishing left–right asymmetry is a fundamental process essential for arrangement of visceral organs during development. In vertebrates, motile cilia-driven fluid flow in the left–right organizer (LRO) is essential for initiating symmetry breaking event. Here, we report that myosin 1d (myo1d) is essential for establishing left–right asymmetry in zebrafish. Using super-resolution microscopy, we show that the zebrafish LRO, Kupffer’s vesicle (KV), fails to form a spherical lumen and establish proper unidirectional flow in the absence of myo1d. This process requires directed vacuolar trafficking in KV epithelial cells. Interestingly, the vacuole transporting function of zebrafish Myo1d can be substituted by myosin1C derived from an ancient eukaryote, Acanthamoeba castellanii, where it regulates the transport of contractile vacuoles. Our findings reveal an evolutionary conserved role for an unconventional myosin in vacuole trafficking, lumen formation, and determining laterality. Nature Publishing Group UK 2018-08-23 /pmc/articles/PMC6107537/ /pubmed/30139971 http://dx.doi.org/10.1038/s41467-018-05866-2 Text en © The Author(s) 2018 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 Saydmohammed, Manush Yagi, Hisato Calderon, Michael Clark, Madeline J. Feinstein, Timothy Sun, Ming Stolz, Donna B. Watkins, Simon C. Amack, Jeffrey D. Lo, Cecilia W. Tsang, Michael Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title | Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title_full | Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title_fullStr | Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title_full_unstemmed | Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title_short | Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
title_sort | vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107537/ https://www.ncbi.nlm.nih.gov/pubmed/30139971 http://dx.doi.org/10.1038/s41467-018-05866-2 |
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