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Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells
Mitochondria are highly pleomorphic, undergoing rounds of fission and fusion. Mitochondria are essential for energy conversion, with fusion favouring higher energy demand. Unlike fission, the molecular components involved in mitochondrial fusion in plants are unknown. Here, we show a role for the GT...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125145/ https://www.ncbi.nlm.nih.gov/pubmed/32246085 http://dx.doi.org/10.1038/s42003-020-0872-x |
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author | White, Rhiannon R. Lin, Congping Leaves, Ian Castro, Inês G. Metz, Jeremy Bateman, Benji C. Botchway, Stanley W. Ward, Andrew D. Ashwin, Peter Sparkes, Imogen |
author_facet | White, Rhiannon R. Lin, Congping Leaves, Ian Castro, Inês G. Metz, Jeremy Bateman, Benji C. Botchway, Stanley W. Ward, Andrew D. Ashwin, Peter Sparkes, Imogen |
author_sort | White, Rhiannon R. |
collection | PubMed |
description | Mitochondria are highly pleomorphic, undergoing rounds of fission and fusion. Mitochondria are essential for energy conversion, with fusion favouring higher energy demand. Unlike fission, the molecular components involved in mitochondrial fusion in plants are unknown. Here, we show a role for the GTPase Miro2 in mitochondria interaction with the ER and its impacts on mitochondria fusion and motility. Mutations in AtMiro2’s GTPase domain indicate that the active variant results in larger, fewer mitochondria which are attached more readily to the ER when compared with the inactive variant. These results are contrary to those in metazoans where Miro predominantly controls mitochondrial motility, with additional GTPases affecting fusion. Synthetically controlling mitochondrial fusion rates could fundamentally change plant physiology by altering the energy status of the cell. Furthermore, altering tethering to the ER could have profound effects on subcellular communication through altering the exchange required for pathogen defence. |
format | Online Article Text |
id | pubmed-7125145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71251452020-04-13 Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells White, Rhiannon R. Lin, Congping Leaves, Ian Castro, Inês G. Metz, Jeremy Bateman, Benji C. Botchway, Stanley W. Ward, Andrew D. Ashwin, Peter Sparkes, Imogen Commun Biol Article Mitochondria are highly pleomorphic, undergoing rounds of fission and fusion. Mitochondria are essential for energy conversion, with fusion favouring higher energy demand. Unlike fission, the molecular components involved in mitochondrial fusion in plants are unknown. Here, we show a role for the GTPase Miro2 in mitochondria interaction with the ER and its impacts on mitochondria fusion and motility. Mutations in AtMiro2’s GTPase domain indicate that the active variant results in larger, fewer mitochondria which are attached more readily to the ER when compared with the inactive variant. These results are contrary to those in metazoans where Miro predominantly controls mitochondrial motility, with additional GTPases affecting fusion. Synthetically controlling mitochondrial fusion rates could fundamentally change plant physiology by altering the energy status of the cell. Furthermore, altering tethering to the ER could have profound effects on subcellular communication through altering the exchange required for pathogen defence. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125145/ /pubmed/32246085 http://dx.doi.org/10.1038/s42003-020-0872-x Text en © The Author(s) 2020 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 White, Rhiannon R. Lin, Congping Leaves, Ian Castro, Inês G. Metz, Jeremy Bateman, Benji C. Botchway, Stanley W. Ward, Andrew D. Ashwin, Peter Sparkes, Imogen Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title | Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title_full | Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title_fullStr | Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title_full_unstemmed | Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title_short | Miro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
title_sort | miro2 tethers the er to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125145/ https://www.ncbi.nlm.nih.gov/pubmed/32246085 http://dx.doi.org/10.1038/s42003-020-0872-x |
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