An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors

Membrane contact sites are regulated through the controlled recruitment of constituent proteins. Yeast vacuolar protein sorting 13 (Vps13) dynamically localizes to membrane contact sites at endosomes, vacuoles, mitochondria, and the endoplasmic reticulum under different cellular conditions and is re...

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Main Authors: Samantha K. Dziurdzik, Björn D.M. Bean, Elizabeth Conibear
Format: Article
Language:English
Published: SAGE Publishing 2018-11-01
Series:Contact
Online Access:https://doi.org/10.1177/2515256418814621
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author Samantha K. Dziurdzik
Björn D.M. Bean
Elizabeth Conibear
author_facet Samantha K. Dziurdzik
Björn D.M. Bean
Elizabeth Conibear
author_sort Samantha K. Dziurdzik
collection DOAJ
description Membrane contact sites are regulated through the controlled recruitment of constituent proteins. Yeast vacuolar protein sorting 13 (Vps13) dynamically localizes to membrane contact sites at endosomes, vacuoles, mitochondria, and the endoplasmic reticulum under different cellular conditions and is recruited to the prospore membrane during meiosis. Prior to our recent work, the mechanism for localization at contact sites was largely unknown. We identified Ypt35 as a novel Vps13 adaptor for endosomes and the nucleus-vacuole junction. Furthermore, we discovered a conserved recruitment motif in Ypt35 and found related motifs in the prospore membrane and mitochondrial adaptors, Spo71 and Mcp1, respectively. All three adaptors compete for binding to a six-repeat region of Vps13, suggesting adaptor competition regulates Vps13 localization. Here, we summarize and discuss the implications of our work, highlighting key outstanding questions.
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spelling doaj.art-bb3922f5d3e344c29880a2b560119a982022-12-22T00:54:19ZengSAGE PublishingContact2515-25642018-11-01110.1177/2515256418814621An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific AdaptorsSamantha K. DziurdzikBjörn D.M. BeanElizabeth ConibearMembrane contact sites are regulated through the controlled recruitment of constituent proteins. Yeast vacuolar protein sorting 13 (Vps13) dynamically localizes to membrane contact sites at endosomes, vacuoles, mitochondria, and the endoplasmic reticulum under different cellular conditions and is recruited to the prospore membrane during meiosis. Prior to our recent work, the mechanism for localization at contact sites was largely unknown. We identified Ypt35 as a novel Vps13 adaptor for endosomes and the nucleus-vacuole junction. Furthermore, we discovered a conserved recruitment motif in Ypt35 and found related motifs in the prospore membrane and mitochondrial adaptors, Spo71 and Mcp1, respectively. All three adaptors compete for binding to a six-repeat region of Vps13, suggesting adaptor competition regulates Vps13 localization. Here, we summarize and discuss the implications of our work, highlighting key outstanding questions.https://doi.org/10.1177/2515256418814621
spellingShingle Samantha K. Dziurdzik
Björn D.M. Bean
Elizabeth Conibear
An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
Contact
title An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
title_full An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
title_fullStr An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
title_full_unstemmed An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
title_short An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
title_sort interorganellar bidding war vps13 localization by competitive organelle specific adaptors
url https://doi.org/10.1177/2515256418814621
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