Open AccessDoa4 directly binds Snf7 to inhibit the recruitment of ESCRT-III remodeling factors
Author(s) -
Dalton Buysse,
Anna-Katharina Pfitzner,
Matt West,
Aurélien Roux,
Greg Odorizzi
Publication year - 2020
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.241455
Subject(s) - escrt , endosome , biology , saccharomyces cerevisiae , protein subunit , microbiology and biotechnology , biogenesis , transport protein , biochemistry , gene , intracellular
The ESCRT-III protein complex executes reverse-topology membrane scission. The scission mechanism is unclear but is linked to remodeling of ESCRT-III complexes at the membrane surface. At endosomes, ESCRT-III mediates the budding of intralumenal vesicles (ILVs). In Saccharomyces cerevisiae, ESCRT-III activity at endosomes is regulated through an unknown mechanism by Doa4, a ubiquitin hydrolase that deubiquitinates transmembrane proteins sorted into ILVs. We report that the non-catalytic N terminus of Doa4 binds Snf7, the predominant ESCRT-III subunit. Through this interaction, Doa4 overexpression alters Snf7 assembly status and inhibits ILV membrane scission. In vitro, the Doa4 N terminus inhibits Snf7 association with Vps2, which functions with Vps24 to arrest Snf7 polymerization and remodel Snf7 polymer structure. In vivo, Doa4 overexpression inhibits Snf7 interaction with Vps2 and with Vps4, an ATPase recruited by Vps2/Vps24 to remodel ESCRT-III complexes by catalyzing subunit turnover. These data suggest a mechanism by which the deubiquitination machinery regulates ILV biogenesis by interfering with ESCRT-III remodeling.