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dc.contributor.authorWhite, RR
dc.contributor.authorLin, C
dc.contributor.authorLeaves, I
dc.contributor.authorCastro, I
dc.contributor.authorMetz, J
dc.contributor.authorBateman, B
dc.contributor.authorBotchway, S
dc.contributor.authorWard, A
dc.contributor.authorAshwin, P
dc.contributor.authorSparkes, I
dc.date.accessioned2020-02-26T09:58:04Z
dc.date.issued2020-04-03
dc.description.abstractMitochondria are essential for energy conversion, and metabolic pathways including photorespiration, biosynthesis of coenzymes and vitamins. They are highly pleomorphic undergoing rounds of fission and fusion through processes coupled with the metabolic status of the cell. For example, fusion favours higher energy demand and, 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. Interaction between these two organelles has been inferred from close positioning. 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.en_GB
dc.description.sponsorshipLeverhulme Trusten_GB
dc.description.sponsorshipScience and Technology Facilities Council (STFC)en_GB
dc.identifier.citationVol. 3 (161). Published online 03 April 2020.en_GB
dc.identifier.doi10.1038/s42003-020-0872-x
dc.identifier.grantnumberRPG-2015-106en_GB
dc.identifier.grantnumberPM-1216en_GB
dc.identifier.urihttp://hdl.handle.net/10871/40991
dc.language.isoenen_GB
dc.publisherNature Researchen_GB
dc.rights© 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/.
dc.subjectmitochondriaen_GB
dc.subjectERen_GB
dc.subjectMiroen_GB
dc.subjectplanten_GB
dc.subjecttetheringen_GB
dc.titleMiro2 tethers the ER to mitochondria to promote mitochondrial fusion in tobacco leaf epidermal cellsen_GB
dc.typeArticleen_GB
dc.date.available2020-02-26T09:58:04Z
dc.identifier.issn2399-3642
dc.descriptionThis is the final version. Available from Nature Research via the DOI in this record. en_GB
dc.descriptionData availability: All data generated or analysed during this study are included in this published article (and its supplementary information files).en_GB
dc.identifier.journalCommunications Biologyen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2020-02-25
exeter.funder::Leverhulme Trusten_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2020-02-25
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-02-25T19:35:30Z
refterms.versionFCDAM
refterms.dateFOA2020-04-09T11:05:40Z
refterms.panelBen_GB


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