ESCRT-mediated vesicle concatenation in plant endosomes

Author:

Buono Rafael Andrade12ORCID,Leier André34ORCID,Paez-Valencia Julio12,Pennington Janice5ORCID,Goodman Kaija12,Miller Nathan1,Ahlquist Paul67859,Marquez-Lago Tatiana T.34,Otegui Marisa S.1210ORCID

Affiliation:

1. Department of Botany, University of Wisconsin-Madison, Madison, WI

2. R.M. Bock Laboratories of Cell and Molecular Biology, University of Wisconsin-Madison, Madison, WI

3. Informatics Institute, School of Medicine, University of Alabama at Birmingham, Birmingham, AL

4. Department of Genetics, School of Medicine, University of Alabama at Birmingham, Birmingham, AL

5. Howard Hughes Medical Institute, Chevy Chase, MD

6. Institute for Molecular Virology, University of Wisconsin-Madison, Madison, WI

7. Departments of Oncology, University of Wisconsin-Madison, Madison, WI

8. Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI

9. Morgridge Institute for Research, Madison, WI

10. Department of Genetics, University of Wisconsin-Madison, Madison, WI

Abstract

Ubiquitinated plasma membrane proteins (cargo) are delivered to endosomes and sorted by endosomal sorting complex required for transport (ESCRT) machinery into endosome intralumenal vesicles (ILVs) for degradation. In contrast to the current model that postulates that ILVs form individually from inward budding of the endosomal limiting membrane, plant ILVs form as networks of concatenated vesicle buds by a novel vesiculation mechanism. We ran computational simulations based on experimentally derived diffusion coefficients of an ESCRT cargo protein and electron tomograms of Arabidopsis thaliana endosomes to measure cargo escape from budding ILVs. We found that 50% of the ESCRT cargo would escape from a single budding profile in 5–20 ms and from three concatenated ILVs in 80–200 ms. These short cargo escape times predict the need for strong diffusion barriers in ILVs. Consistent with a potential role as a diffusion barrier, we find that the ESCRT-III protein SNF7 remains associated with ILVs and is delivered to the vacuole for degradation.

Funder

Howard Hughes Medical Institute

National Science Foundation

University of Wisconsin-Madison

Publisher

Rockefeller University Press

Subject

Cell Biology

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