%0 Journal Article %A Vincent Anton %A Ira Buntenbroich %A Ramona Schuster %A Felix Babatz %A Tânia Simões %A Selver Altin %A Gaetano Calabrese %A Jan Riemer %A Astrid Schauss %A Mafalda Escobar-Henriques %T Plasticity in salt bridge allows fusion-competent ubiquitylation of mitofusins and Cdc48 recognition %D 2019 %R 10.26508/lsa.201900491 %J Life Science Alliance %P e201900491 %V 2 %N 6 %X Mitofusins are dynamin-related GTPases that drive mitochondrial fusion by sequential events of oligomerization and GTP hydrolysis, followed by their ubiquitylation. Here, we show that fusion requires a trilateral salt bridge at a hinge point of the yeast mitofusin Fzo1, alternatingly forming before and after GTP hydrolysis. Mutations causative of Charcot–Marie–Tooth disease massively map to this hinge point site, underlining the disease relevance of the trilateral salt bridge. A triple charge swap rescues the activity of Fzo1, emphasizing the close coordination of the hinge residues with GTP hydrolysis. Subsequently, ubiquitylation of Fzo1 allows the AAA-ATPase ubiquitin-chaperone Cdc48 to resolve Fzo1 clusters, releasing the dynamin for the next fusion round. Furthermore, cross-complementation within the oligomer unexpectedly revealed ubiquitylated but fusion-incompetent Fzo1 intermediates. However, Cdc48 did not affect the ubiquitylated but fusion-incompetent variants, indicating that Fzo1 ubiquitylation is only controlled after membrane merging. Together, we present an integrated model on how mitochondrial outer membranes fuse, a critical process for their respiratory function but also putatively relevant for therapeutic interventions. %U https://www.life-science-alliance.org/content/lsa/2/6/e201900491.full.pdf