Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport

Abstract Co-assembly of the multilayered coat protein complex II (COPII) with the Sar1 GTPase at subdomains of the endoplasmic reticulum (ER) enables secretory cargoes to be concentrated efficiently within nascent transport intermediates, which subsequently deliver their contents to ER-Golgi interme...

Full description

Bibliographic Details
Main Authors: William Kasberg, Peter Luong, Kevin A. Swift, Anjon Audhya
Format: Article
Language:English
Published: Nature Portfolio 2023-12-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-44002-7
_version_ 1797397909412511744
author William Kasberg
Peter Luong
Kevin A. Swift
Anjon Audhya
author_facet William Kasberg
Peter Luong
Kevin A. Swift
Anjon Audhya
author_sort William Kasberg
collection DOAJ
description Abstract Co-assembly of the multilayered coat protein complex II (COPII) with the Sar1 GTPase at subdomains of the endoplasmic reticulum (ER) enables secretory cargoes to be concentrated efficiently within nascent transport intermediates, which subsequently deliver their contents to ER-Golgi intermediate compartments. Here, we define the spatiotemporal accumulation of native COPII subunits and secretory cargoes at ER subdomains under differing nutrient availability conditions using a combination of CRISPR/Cas9-mediated genome editing and live cell imaging. Our findings demonstrate that the rate of inner COPII coat recruitment serves as a determinant for the pace of cargo export, irrespective of COPII subunit expression levels. Moreover, increasing inner COPII coat recruitment kinetics is sufficient to rescue cargo trafficking deficits caused by acute nutrient limitation. Our findings are consistent with a model in which the rate of inner COPII coat addition acts as an important control point to regulate cargo export from the ER.
first_indexed 2024-03-09T01:18:01Z
format Article
id doaj.art-d87785dbd50f41fd890b1ed16e6baf04
institution Directory Open Access Journal
issn 2041-1723
language English
last_indexed 2024-03-09T01:18:01Z
publishDate 2023-12-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj.art-d87785dbd50f41fd890b1ed16e6baf042023-12-10T12:24:12ZengNature PortfolioNature Communications2041-17232023-12-0114111310.1038/s41467-023-44002-7Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transportWilliam Kasberg0Peter Luong1Kevin A. Swift2Anjon Audhya3Department of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public HealthDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public HealthDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public HealthDepartment of Biomolecular Chemistry, University of Wisconsin School of Medicine and Public HealthAbstract Co-assembly of the multilayered coat protein complex II (COPII) with the Sar1 GTPase at subdomains of the endoplasmic reticulum (ER) enables secretory cargoes to be concentrated efficiently within nascent transport intermediates, which subsequently deliver their contents to ER-Golgi intermediate compartments. Here, we define the spatiotemporal accumulation of native COPII subunits and secretory cargoes at ER subdomains under differing nutrient availability conditions using a combination of CRISPR/Cas9-mediated genome editing and live cell imaging. Our findings demonstrate that the rate of inner COPII coat recruitment serves as a determinant for the pace of cargo export, irrespective of COPII subunit expression levels. Moreover, increasing inner COPII coat recruitment kinetics is sufficient to rescue cargo trafficking deficits caused by acute nutrient limitation. Our findings are consistent with a model in which the rate of inner COPII coat addition acts as an important control point to regulate cargo export from the ER.https://doi.org/10.1038/s41467-023-44002-7
spellingShingle William Kasberg
Peter Luong
Kevin A. Swift
Anjon Audhya
Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
Nature Communications
title Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
title_full Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
title_fullStr Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
title_full_unstemmed Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
title_short Nutrient deprivation alters the rate of COPII subunit recruitment at ER subdomains to tune secretory protein transport
title_sort nutrient deprivation alters the rate of copii subunit recruitment at er subdomains to tune secretory protein transport
url https://doi.org/10.1038/s41467-023-44002-7
work_keys_str_mv AT williamkasberg nutrientdeprivationalterstherateofcopiisubunitrecruitmentatersubdomainstotunesecretoryproteintransport
AT peterluong nutrientdeprivationalterstherateofcopiisubunitrecruitmentatersubdomainstotunesecretoryproteintransport
AT kevinaswift nutrientdeprivationalterstherateofcopiisubunitrecruitmentatersubdomainstotunesecretoryproteintransport
AT anjonaudhya nutrientdeprivationalterstherateofcopiisubunitrecruitmentatersubdomainstotunesecretoryproteintransport