ESCRT‐III and Vps4: a dynamic multipurpose tool for membrane budding and scission. (8th March 2016)

• Record Type: Journal Article
• Authors: Alonso Y Adell, Manuel; Migliano, Simona M.; Teis, David
• Is Part Of: FEBS journal. Volume 283:Number 18(2016)
• Page Start: 3288
• Page End: 3302
• Publication Date: 2016-03-08
• Subjects: adaptors -- ESCRT‐III -- membrane remodelling -- Vps4 AAA‐ATPase; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 572
• DOI: 10.1111/febs.13688
• Languages: English
• ISSNs: 1742-464X

Abstract

Abstract : Complex molecular machineries bud, scission and repair cellular membranes. Components of the multi‐subunit endosomal sorting complex required for transport (ESCRT) machinery are enlisted when multivesicular bodies are generated, extracellular vesicles are formed, the plasma membrane needs to be repaired, enveloped viruses bud out of host cells, defective nuclear pores have to be cleared, the nuclear envelope must be resealed after mitosis and for final midbody abscission during cytokinesis. While some ESCRT components are only required for specific processes, the assembly of ESCRT‐III polymers on target membranes and the action of the AAA‐ATPase Vps4 are mandatory for every process. In this review, we summarize the current knowledge of structural and functional features of ESCRT‐III/Vps4 assemblies in the growing pantheon of ESCRT‐dependent pathways. We describe specific recruitment processes for ESCRT‐III to different membranes, which could be useful to selectively inhibit ESCRT function during specific processes, while not affecting other ESCRT‐dependent processes. Finally, we speculate how ESCRT‐III and Vps4 might function together and highlight how the characterization of their precise spatiotemporal organization will improve our understanding of ESCRT‐mediated membrane budding and scission in vivo . Abstract : We discuss how ESCRT‐III and Vps4 could function together to remodel membranes when multivesicular bodies are generated, extracellular vesicles are formed, the plasma membrane needs to be repaired, enveloped virus bud out of host cells, defective nuclear pores have to be cleared, the nuclear envelope must be resealed after mitosis and during final midbody abscission during cytokinesis.