Acylation – A New Means to Control Traffic Through the Golgi

The Golgi is well known to act as center for modification and sorting of proteins for secretion and delivery to other organelles. A key sorting step occurs at the trans-Golgi network and is mediated by protein adapters. However, recent data indicate that sorting also occurs much earlier, at the cis-...

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Main Authors: Andreas M. Ernst, Derek Toomre, Jonathan S. Bogan
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fcell.2019.00109/full
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spelling doaj-ef727070745c42caaf7997f5f0652e482020-11-25T01:28:15ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2019-06-01710.3389/fcell.2019.00109465300Acylation – A New Means to Control Traffic Through the GolgiAndreas M. Ernst0Derek Toomre1Jonathan S. Bogan2Jonathan S. Bogan3Department of Cell Biology, Yale School of Medicine, Yale University, New Haven, CT, United StatesDepartment of Cell Biology, Yale School of Medicine, Yale University, New Haven, CT, United StatesDepartment of Cell Biology, Yale School of Medicine, Yale University, New Haven, CT, United StatesSection of Endocrinology and Metabolism, Department of Internal Medicine, Yale School of Medicine, Yale University, New Haven, CT, United StatesThe Golgi is well known to act as center for modification and sorting of proteins for secretion and delivery to other organelles. A key sorting step occurs at the trans-Golgi network and is mediated by protein adapters. However, recent data indicate that sorting also occurs much earlier, at the cis-Golgi, and uses lipid acylation as a novel means to regulate anterograde flux. Here, we examine an emerging role of S-palmitoylation/acylation as a mechanism to regulate anterograde routing. We discuss the critical Golgi-localized DHHC S-palmitoyltransferase enzymes that orchestrate this lipid modification, as well as their diverse protein clients (e.g., MAP6, SNAP25, CSP, LAT, β-adrenergic receptors, GABA receptors, and GLUT4 glucose transporters). Critically, for integral membrane proteins, S-acylation can act as new a “self-sorting” signal to concentrate these cargoes in rims of Golgi cisternae, and to promote their rapid traffic through the Golgi or, potentially, to bypass the Golgi. We discuss this mechanism and examine its potential relevance to human physiology and disease, including diabetes and neurodegenerative diseases.https://www.frontiersin.org/article/10.3389/fcell.2019.00109/fullGolgipalmitoylationacylationanterograde transportGolgi bypassmembrane traffic
collection DOAJ
language English
format Article
sources DOAJ
author Andreas M. Ernst
Derek Toomre
Jonathan S. Bogan
Jonathan S. Bogan
spellingShingle Andreas M. Ernst
Derek Toomre
Jonathan S. Bogan
Jonathan S. Bogan
Acylation – A New Means to Control Traffic Through the Golgi
Frontiers in Cell and Developmental Biology
Golgi
palmitoylation
acylation
anterograde transport
Golgi bypass
membrane traffic
author_facet Andreas M. Ernst
Derek Toomre
Jonathan S. Bogan
Jonathan S. Bogan
author_sort Andreas M. Ernst
title Acylation – A New Means to Control Traffic Through the Golgi
title_short Acylation – A New Means to Control Traffic Through the Golgi
title_full Acylation – A New Means to Control Traffic Through the Golgi
title_fullStr Acylation – A New Means to Control Traffic Through the Golgi
title_full_unstemmed Acylation – A New Means to Control Traffic Through the Golgi
title_sort acylation – a new means to control traffic through the golgi
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2019-06-01
description The Golgi is well known to act as center for modification and sorting of proteins for secretion and delivery to other organelles. A key sorting step occurs at the trans-Golgi network and is mediated by protein adapters. However, recent data indicate that sorting also occurs much earlier, at the cis-Golgi, and uses lipid acylation as a novel means to regulate anterograde flux. Here, we examine an emerging role of S-palmitoylation/acylation as a mechanism to regulate anterograde routing. We discuss the critical Golgi-localized DHHC S-palmitoyltransferase enzymes that orchestrate this lipid modification, as well as their diverse protein clients (e.g., MAP6, SNAP25, CSP, LAT, β-adrenergic receptors, GABA receptors, and GLUT4 glucose transporters). Critically, for integral membrane proteins, S-acylation can act as new a “self-sorting” signal to concentrate these cargoes in rims of Golgi cisternae, and to promote their rapid traffic through the Golgi or, potentially, to bypass the Golgi. We discuss this mechanism and examine its potential relevance to human physiology and disease, including diabetes and neurodegenerative diseases.
topic Golgi
palmitoylation
acylation
anterograde transport
Golgi bypass
membrane traffic
url https://www.frontiersin.org/article/10.3389/fcell.2019.00109/full
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