VPS13D interacts with VCP/p97 and negatively regulates endoplasmic reticulum–mitochondria interactions |
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| Authors: | Yuanjiao Du Jingru Wang Juan Xiong Na Fang Wei-Ke Ji |
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| Affiliation: | University of Gothenburg;aDepartment of Biochemistry and Molecular Biology, School of Basic Medicine;bDepartment of Anesthesiology, Tongji Hospital, Tongji Medical College, and;cCell Architecture Research Institute, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China |
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| Abstract: | Membrane contact sites (MCSs) between the endoplasmic reticulum (ER) and mitochondria are emerging as critical hubs for diverse cellular events, and alterations in the extent of these contacts are linked to neurodegenerative diseases. However, the mechanisms that control ER–mitochondria interactions are so far elusive. Here, we demonstrate a key role of vacuolar protein sorting–associated protein 13D (VPS13D) in the negative regulation of ER–mitochondria MCSs. VPS13D suppression results in extensive ER–mitochondria tethering, a phenotype that can be substantially rescued by suppression of the tethering proteins VAPB and PTPIP51. VPS13D interacts with valosin-containing protein (VCP/p97) to control the level of ER-resident VAPB at contacts. VPS13D is required for the stability of p97. Functionally, VPS13D suppression leads to severe defects in mitochondrial morphology, mitochondrial cellular distribution, and mitochondrial DNA synthesis. Together, our results suggest that VPS13D negatively regulates the ER–mitochondria MCSs, partially through its interactions with VCP/p97. |
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