Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1464
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dc.contributor.authorKAMERKAR, SUKRUT C.en_US
dc.contributor.authorKraus, Felixen_US
dc.contributor.authorSharpe, Alice J.en_US
dc.contributor.authorPUCADYIL, THOMAS J.en_US
dc.contributor.authorRyan, Michael T.en_US
dc.date.accessioned2018-12-28T06:58:28Z
dc.date.available2018-12-28T06:58:28Z
dc.date.issued2018-12en_US
dc.identifier.citationNature Communications, Vol. 9en_US
dc.identifier.issn2041-1723en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1464-
dc.identifier.urihttps://doi.org/10.1038/s41467-018-07543-wen_US
dc.description.abstractDynamin-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.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.subjectMembrane fissionen_US
dc.subjectMembrane lipidsen_US
dc.subjectMitochondriaen_US
dc.subjectTOC-DEC-2018en_US
dc.subject2018en_US
dc.titleDynamin-related protein 1 has membrane constricting and severing abilities sufficient for mitochondrial and peroxisomal fissionen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleNature Communicationsen_US
dc.publication.originofpublisherForeignen_US
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