Iwona I. Smaczynska-de Rooij
Phosphorylation Regulates the Endocytic Function of the Yeast Dynamin-Related Protein Vps1
Smaczynska-de Rooij, Iwona I.; Marklew, Christopher J.; Allwood, Ellen G.; Palmer, Sarah E.; Booth, Wesley I.; Mishra, Ritu; Goldberg, Martin W.; Ayscough, Kathryn R.
Authors
Christopher J. Marklew
Ellen G. Allwood
Sarah E. Palmer
Wesley I. Booth
Ritu Mishra
Professor Martin Goldberg m.w.goldberg@durham.ac.uk
Professor
Kathryn R. Ayscough
Abstract
The family of dynamin proteins is known to function in many eukaryotic membrane fusion and fission events. The yeast dynamin-related protein Vps1 functions at several stages of membrane trafficking, including Golgi apparatus to endosome and vacuole, peroxisomal fission, and endocytic scission. We have previously shown that in its endocytic role, Vps1 functions with the amphiphysin heterodimer Rvs161/Rvs167 to facilitate scission and release of vesicles. Phosphoproteome studies of Saccharomyces cerevisiae have identified a phosphorylation site in Vps1 at serine 599. In this study, we confirmed this phosphorylation event, and we reveal that, like Rvs167, Vps1 can be phosphorylated by the yeast cyclin-associated kinase Pho85 in vivo and in vitro. The importance of this posttranslational modification was revealed when mutagenesis of S599 to a phosphomimetic or nonphosphorylatable form caused defects in endocytosis but not in other functions associated with Vps1. Mutation to nonphosphorylatable valine inhibited the Rvs167 interaction, while both S599V and S599D caused defects in vesicle scission, as shown by both live-cell imaging and electron microscopy of endocytic invaginations. Our data support a model in which phosphorylation and dephosphorylation of Vps1 promote distinct interactions and highlight the importance of such regulatory events in facilitating sequential progression of the endocytic process.
Citation
Smaczynska-de Rooij, I. I., Marklew, C. J., Allwood, E. G., Palmer, S. E., Booth, W. I., Mishra, R., …Ayscough, K. R. (2016). Phosphorylation Regulates the Endocytic Function of the Yeast Dynamin-Related Protein Vps1. Molecular and Cellular Biology, 36(5), 742-755. https://doi.org/10.1128/mcb.00833-15
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 10, 2015 |
Online Publication Date | Dec 28, 2015 |
Publication Date | Mar 1, 2016 |
Deposit Date | Jun 23, 2017 |
Publicly Available Date | Jun 23, 2017 |
Journal | Molecular and Cellular Biology |
Print ISSN | 0270-7306 |
Electronic ISSN | 1098-5549 |
Publisher | American Society for Microbiology |
Peer Reviewed | Peer Reviewed |
Volume | 36 |
Issue | 5 |
Pages | 742-755 |
DOI | https://doi.org/10.1128/mcb.00833-15 |
Public URL | https://durham-repository.worktribe.com/output/1384194 |
Files
Published Journal Article
(2.9 Mb)
PDF
Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/
Copyright Statement
Copyright © 2016 Smaczynska-de Rooij et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license.
You might also like
STING nuclear partners contribute to innate immune signaling responses
(2021)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search