Campus Units

Biomedical Sciences

Document Type

Article

Publication Version

Accepted Manuscript

Publication Date

1-22-2020

Journal or Book Title

Cell Stress and Chaperones

DOI

10.1007/s12192-019-01062-3

Abstract

Coat protein complex II (COPII) plays an essential role in the export of cargo molecules such as secretory proteins, membrane proteins, and lipids from the endoplasmic reticulum (ER). In yeast, the COPII machinery is critical for cell viability as most COPII knockout mutants fail to survive. In mice and fish, homozygous knockout mutants of most COPII genes are embryonic lethal, reflecting the essentiality of the COPII machinery in the early stages of vertebrate development. In humans, COPII mutations, which are often hypomorphic, cause diseases having distinct clinical features. This is interesting as the fundamental cellular defect of these diseases, that is, failure of ER export, is similar. Analyses of humans and animals carrying COPII mutations have revealed clues to why a similar ER export defect can cause such different diseases. Previous reviews have focused mainly on the deficit of secretory or membrane proteins in the final destinations because of an ER export block. In this review, we also underscore the other consequence of the ER export block, namely ER stress triggered by the accumulation of cargo proteins in the ER.

Comments

This is a post-peer-review, pre-copyedit version of an article published in Cell Stress and Chaperones. The final authenticated version is available online at DOI: 10.1007/s12192-019-01062-3. Posted with permission.

Copyright Owner

Springer Nature

Language

en

File Format

application/pdf

Available for download on Friday, January 22, 2021

Published Version

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