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Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213

Mysterin (also known as RNF213) is a huge intracellular protein with two AAA+ ATPase modules and a RING finger ubiquitin ligase domain. Mysterin was originally isolated as a significant risk factor for the cryptogenic cerebrovascular disorder moyamoya disease, and was found to be involved in physiol...

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Autores principales: Kotani, Yuri, Morito, Daisuke, Yamazaki, Satoru, Ogino, Kazutoyo, Kawakami, Koichi, Takashima, Seiji, Hirata, Hiromi, Nagata, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632019/
https://www.ncbi.nlm.nih.gov/pubmed/26530008
http://dx.doi.org/10.1038/srep16161
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author Kotani, Yuri
Morito, Daisuke
Yamazaki, Satoru
Ogino, Kazutoyo
Kawakami, Koichi
Takashima, Seiji
Hirata, Hiromi
Nagata, Kazuhiro
author_facet Kotani, Yuri
Morito, Daisuke
Yamazaki, Satoru
Ogino, Kazutoyo
Kawakami, Koichi
Takashima, Seiji
Hirata, Hiromi
Nagata, Kazuhiro
author_sort Kotani, Yuri
collection PubMed
description Mysterin (also known as RNF213) is a huge intracellular protein with two AAA+ ATPase modules and a RING finger ubiquitin ligase domain. Mysterin was originally isolated as a significant risk factor for the cryptogenic cerebrovascular disorder moyamoya disease, and was found to be involved in physiological angiogenesis in zebrafish. However, the function and the physiological significance of mysterin in other than blood vessels remain largely unknown, although mysterin is ubiquitously expressed in animal tissues. In this study, we performed antisense-mediated suppression of a mysterin orthologue in zebrafish larvae and revealed that mysterin-deficient larvae showed significant reduction in fast myofibrils and immature projection of primary motoneurons, leading to severe motor deficits. Fast muscle-specific restoration of mysterin expression cancelled these phenotypes, and interestingly both AAA+ ATPase and ubiquitin ligase activities of mysterin were indispensable for proper fast muscle formation, demonstrating an essential role of mysterin and its enzymatic activities in the neuromuscular regulation in zebrafish.
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spelling pubmed-46320192015-12-07 Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213 Kotani, Yuri Morito, Daisuke Yamazaki, Satoru Ogino, Kazutoyo Kawakami, Koichi Takashima, Seiji Hirata, Hiromi Nagata, Kazuhiro Sci Rep Article Mysterin (also known as RNF213) is a huge intracellular protein with two AAA+ ATPase modules and a RING finger ubiquitin ligase domain. Mysterin was originally isolated as a significant risk factor for the cryptogenic cerebrovascular disorder moyamoya disease, and was found to be involved in physiological angiogenesis in zebrafish. However, the function and the physiological significance of mysterin in other than blood vessels remain largely unknown, although mysterin is ubiquitously expressed in animal tissues. In this study, we performed antisense-mediated suppression of a mysterin orthologue in zebrafish larvae and revealed that mysterin-deficient larvae showed significant reduction in fast myofibrils and immature projection of primary motoneurons, leading to severe motor deficits. Fast muscle-specific restoration of mysterin expression cancelled these phenotypes, and interestingly both AAA+ ATPase and ubiquitin ligase activities of mysterin were indispensable for proper fast muscle formation, demonstrating an essential role of mysterin and its enzymatic activities in the neuromuscular regulation in zebrafish. Nature Publishing Group 2015-11-04 /pmc/articles/PMC4632019/ /pubmed/26530008 http://dx.doi.org/10.1038/srep16161 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kotani, Yuri
Morito, Daisuke
Yamazaki, Satoru
Ogino, Kazutoyo
Kawakami, Koichi
Takashima, Seiji
Hirata, Hiromi
Nagata, Kazuhiro
Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title_full Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title_fullStr Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title_full_unstemmed Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title_short Neuromuscular regulation in zebrafish by a large AAA+ ATPase/ubiquitin ligase, mysterin/RNF213
title_sort neuromuscular regulation in zebrafish by a large aaa+ atpase/ubiquitin ligase, mysterin/rnf213
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632019/
https://www.ncbi.nlm.nih.gov/pubmed/26530008
http://dx.doi.org/10.1038/srep16161
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