Department of Anesthesiology

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Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.

TitleDynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.
Publication TypeJournal Article
Year of Publication2017
AuthorsMierzwa BE, Chiaruttini N, Redondo-Morata L, von Filseck JMoser, König J, Larios J, Poser I, Müller-Reichert T, Scheuring S, Roux A, Gerlich DW
JournalNat Cell Biol
Volume19
Issue7
Pagination787-798
Date Published2017 Jul
ISSN1476-4679
Abstract

The endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes.

DOI10.1038/ncb3559
Alternate JournalNat. Cell Biol.
PubMed ID28604678
PubMed Central IDPMC5493987