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Dynamin-related protein 1 has membrane constricting and severing abilities sufficient for mitochondrial and peroxisomal fission

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dc.contributor.author KAMERKAR, SUKRUT C. en_US
dc.contributor.author Kraus, Felix en_US
dc.contributor.author Sharpe, Alice J. en_US
dc.contributor.author PUCADYIL, THOMAS J. en_US
dc.contributor.author Ryan, Michael T. en_US
dc.date.accessioned 2018-12-28T06:58:28Z
dc.date.available 2018-12-28T06:58:28Z
dc.date.issued 2018-12 en_US
dc.identifier.citation Nature Communications, Vol. 9 en_US
dc.identifier.issn 2041-1723 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1464
dc.identifier.uri https://doi.org/10.1038/s41467-018-07543-w en_US
dc.description.abstract Dynamin-related protein 1 (Drp1) is essential for mitochondrial and peroxisomal fission. Recent studies propose that Drp1 does not sever but rather constricts mitochondrial membranes allowing dynamin 2 (Dnm2) to execute final scission. Here, we report that unlike Drp1, Dnm2 is dispensable for peroxisomal and mitochondrial fission, as these events occurred in Dnm2 knockout cells. Fission events were also observed in mouse embryonic fibroblasts lacking Dnm1, 2 and 3. Using reconstitution experiments on preformed membrane tubes, we show that Drp1 alone both constricts and severs membrane tubes. Scission required the membrane binding, self-assembling and GTPase activities of Drp1 and occurred on tubes up to 250-nm in radius. In contrast, Dnm2 exhibited severely restricted fission capacity with occasional severing of tubes below 50-nm in radius. We conclude that Drp1 has both membrane constricting and severing abilities and is the dominant dynamin performing mitochondrial and peroxisomal fission. en_US
dc.language.iso en en_US
dc.publisher Nature Publishing Group en_US
dc.subject Membrane fission en_US
dc.subject Membrane lipids en_US
dc.subject Mitochondria en_US
dc.subject TOC-DEC-2018 en_US
dc.subject 2018 en_US
dc.title Dynamin-related protein 1 has membrane constricting and severing abilities sufficient for mitochondrial and peroxisomal fission en_US
dc.type Article en_US
dc.contributor.department Dept. of Biology en_US
dc.identifier.sourcetitle Nature Communications en_US
dc.publication.originofpublisher Foreign en_US


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