Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783349982938529792
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
work_keys_str_mv AT saydmohammedmanush vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT yagihisato vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT calderonmichael vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT clarkmadelinej vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT feinsteintimothy vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT sunming vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT stolzdonnab vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT watkinssimonc vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT amackjeffreyd vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT loceciliaw vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality
AT tsangmichael vertebratemyosin1dregulatesleftrightorganizermorphogenesisandlaterality