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. 2020 Nov 3;78(5):1929–1941. doi: 10.1007/s00018-020-03687-5

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — The role of Miro1 in peroxisomal and mitochondrial dynamics. Peroxisomes and mitochondria share a Drp1-dependent fission machinery, with the recruitment of Drp1 to either organelle being negatively regulated by Miro. Conversely, the microtubule-dependent transport of peroxisomes and mitochondria uses different machineries, thus it is currently unclear if the role of Miro1 on these processes is identical. Adaptors—unknown, likely PEX1 for KIFC3, TRAK2 for KIF5 and Pex14 for dynein; receptor—unknown, possibly mitofusins and Armcx1/3