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Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production
Mitochondrial fusion and fission affect the distribution and quality control of mitochondria. We show that Marf (Mitochondrial associated regulatory factor), is required for mitochondrial fusion and transport in long axons. Moreover, loss of Marf leads to a severe depletion of mitochondria in neurom...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215535/ https://www.ncbi.nlm.nih.gov/pubmed/25313867 http://dx.doi.org/10.7554/eLife.03558 |
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author | Sandoval, Hector Yao, Chi-Kuang Chen, Kuchuan Jaiswal, Manish Donti, Taraka Lin, Yong Qi Bayat, Vafa Xiong, Bo Zhang, Ke David, Gabriela Charng, Wu-Lin Yamamoto, Shinya Duraine, Lita Graham, Brett H Bellen, Hugo J |
author_facet | Sandoval, Hector Yao, Chi-Kuang Chen, Kuchuan Jaiswal, Manish Donti, Taraka Lin, Yong Qi Bayat, Vafa Xiong, Bo Zhang, Ke David, Gabriela Charng, Wu-Lin Yamamoto, Shinya Duraine, Lita Graham, Brett H Bellen, Hugo J |
author_sort | Sandoval, Hector |
collection | PubMed |
description | Mitochondrial fusion and fission affect the distribution and quality control of mitochondria. We show that Marf (Mitochondrial associated regulatory factor), is required for mitochondrial fusion and transport in long axons. Moreover, loss of Marf leads to a severe depletion of mitochondria in neuromuscular junctions (NMJs). Marf mutants also fail to maintain proper synaptic transmission at NMJs upon repetitive stimulation, similar to Drp1 fission mutants. However, unlike Drp1, loss of Marf leads to NMJ morphology defects and extended larval lifespan. Marf is required to form contacts between the endoplasmic reticulum and/or lipid droplets (LDs) and for proper storage of cholesterol and ecdysone synthesis in ring glands. Interestingly, human Mitofusin-2 rescues the loss of LD but both Mitofusin-1 and Mitofusin-2 are required for steroid-hormone synthesis. Our data show that Marf and Mitofusins share an evolutionarily conserved role in mitochondrial transport, cholesterol ester storage and steroid-hormone synthesis. DOI: http://dx.doi.org/10.7554/eLife.03558.001 |
format | Online Article Text |
id | pubmed-4215535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42155352014-11-21 Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production Sandoval, Hector Yao, Chi-Kuang Chen, Kuchuan Jaiswal, Manish Donti, Taraka Lin, Yong Qi Bayat, Vafa Xiong, Bo Zhang, Ke David, Gabriela Charng, Wu-Lin Yamamoto, Shinya Duraine, Lita Graham, Brett H Bellen, Hugo J eLife Developmental Biology and Stem Cells Mitochondrial fusion and fission affect the distribution and quality control of mitochondria. We show that Marf (Mitochondrial associated regulatory factor), is required for mitochondrial fusion and transport in long axons. Moreover, loss of Marf leads to a severe depletion of mitochondria in neuromuscular junctions (NMJs). Marf mutants also fail to maintain proper synaptic transmission at NMJs upon repetitive stimulation, similar to Drp1 fission mutants. However, unlike Drp1, loss of Marf leads to NMJ morphology defects and extended larval lifespan. Marf is required to form contacts between the endoplasmic reticulum and/or lipid droplets (LDs) and for proper storage of cholesterol and ecdysone synthesis in ring glands. Interestingly, human Mitofusin-2 rescues the loss of LD but both Mitofusin-1 and Mitofusin-2 are required for steroid-hormone synthesis. Our data show that Marf and Mitofusins share an evolutionarily conserved role in mitochondrial transport, cholesterol ester storage and steroid-hormone synthesis. DOI: http://dx.doi.org/10.7554/eLife.03558.001 eLife Sciences Publications, Ltd 2014-10-14 /pmc/articles/PMC4215535/ /pubmed/25313867 http://dx.doi.org/10.7554/eLife.03558 Text en Copyright © 2014, Sandoval et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Sandoval, Hector Yao, Chi-Kuang Chen, Kuchuan Jaiswal, Manish Donti, Taraka Lin, Yong Qi Bayat, Vafa Xiong, Bo Zhang, Ke David, Gabriela Charng, Wu-Lin Yamamoto, Shinya Duraine, Lita Graham, Brett H Bellen, Hugo J Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title | Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title_full | Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title_fullStr | Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title_full_unstemmed | Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title_short | Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
title_sort | mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215535/ https://www.ncbi.nlm.nih.gov/pubmed/25313867 http://dx.doi.org/10.7554/eLife.03558 |
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