Design principles of the ESCRT-III Vps24-Vps2 module

Author:

Banjade Sudeep12ORCID,Shah Yousuf H12,Tang Shaogeng3ORCID,Emr Scott D12ORCID

Affiliation:

1. Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States

2. Department of Molecular Biology and Genetics, Cornell University, Ithaca, United States

3. Department of Biochemistry, Stanford University, Stanford, United States

Abstract

ESCRT-III polymerization is required for all endosomal sorting complex required for transport (ESCRT)-dependent events in the cell. However, the relative contributions of the eight ESCRT-III subunits differ between each process. The minimal features of ESCRT-III proteins necessary for function and the role for the multiple ESCRT-III subunits remain unclear. To identify essential features of ESCRT-III subunits, we previously studied the polymerization mechanisms of two ESCRT-III subunits Snf7 and Vps24, identifying the association of the helix-4 region of Snf7 with the helix-1 region of Vps24 (Banjade et al., 2019a). Here, we find that mutations in the helix-1 region of another ESCRT-III subunit Vps2 can functionally replace Vps24 in Saccharomyces cerevisiae. Engineering and genetic selections revealed the required features of both subunits. Our data allow us to propose three minimal features required for ESCRT-III function – spiral formation, lateral association of the spirals through heteropolymerization, and binding to the AAA + ATPase Vps4 for dynamic remodeling.

Funder

Damon Runyon Cancer Research Foundation

Cornell University

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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