Abstract |
Upon amino acid (AA) starvation and TOR inactivation, plasma-membrane-localized permeases rapidly undergo ubiquitination and internalization via the vacuolar protein sorting/multivesicular body (VPS-MVB) pathway and are degraded in the yeast vacuole. We now show that specific Golgi proteins are also directed to the vacuole under these conditions as part of a Golgi quality-control (GQC) process. The degradation of GQC substrates is dependent upon ubiquitination by the defective-for-SREBP-cleavage (DSC) complex, which was identified via genetic screening and includes the Tul1 E3 ligase. Using a model GQC substrate, GFP-tagged Yif1, we show that vacuolar targeting necessitates upregulation of the VPS pathway via proteasome-mediated degradation of the initial endosomal sorting complex required for transport, ESCRT-0, but not downstream ESCRT components. Thus, early cellular responses to starvation include the targeting of specific Golgi proteins for degradation, a phenomenon reminiscent of the inactivation of BTN1, the yeast Batten disease gene ortholog.
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Authors | Niv Dobzinski, Silvia G Chuartzman, Rachel Kama, Maya Schuldiner, Jeffrey E Gerst |
Journal | Cell reports
(Cell Rep)
Vol. 12
Issue 11
Pg. 1876-86
(Sep 22 2015)
ISSN: 2211-1247 [Electronic] United States |
PMID | 26344761
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Adaptor Proteins, Vesicular Transport
- Endosomal Sorting Complexes Required for Transport
- Saccharomyces cerevisiae Proteins
- YIF1 protein, S cerevisiae
- Ubc4 protein, S cerevisiae
- Ubiquitin-Conjugating Enzymes
- TOR Serine-Threonine Kinases
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Topics |
- Adaptor Proteins, Vesicular Transport
(metabolism)
- Endosomal Sorting Complexes Required for Transport
(genetics, metabolism)
- Golgi Apparatus
(enzymology, metabolism)
- Protein Transport
- Quality Control
- Saccharomyces cerevisiae
(genetics, metabolism)
- Saccharomyces cerevisiae Proteins
(metabolism)
- Signal Transduction
- TOR Serine-Threonine Kinases
(metabolism)
- Ubiquitin-Conjugating Enzymes
(metabolism)
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