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Auto-regulation of Secretory Flux by Sensing and Responding to the Folded Cargo Protein Load in the Endoplasmic Reticulum
Author(s) -
Advait Subramanian,
Anita Capalbo,
Namrata Ravi Iyengar,
Riccardo Rizzo,
Antonella Di Campli,
Rosaria Di Martino,
Matteo Lo Monte,
Andrea R. Beccari,
Amol Yerudkar,
Carmen Del Vecchio,
Luigi Glielmo,
Gabriele Turacchio,
Marinella Pirozzi,
Sang Geon Kim,
Petra Henklein,
Jorge Cancino,
Seetharaman Parashuraman,
Dario Diviani,
Francesca Fanelli,
Michele Sallese,
Alberto Luini
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.01.035
Subject(s) - endoplasmic reticulum , microbiology and biotechnology , copii , biology , secretory pathway , secretory protein , guanine nucleotide exchange factor , secretion , flux (metallurgy) , signal transduction , golgi apparatus , biochemistry , chemistry , organic chemistry
Maintaining the optimal performance of cell processes and organelles is the task of auto-regulatory systems. Here we describe an auto-regulatory device that helps to maintain homeostasis of the endoplasmic reticulum (ER) by adjusting the secretory flux to the cargo load. The cargo-recruiting subunit of the coatomer protein II (COPII) coat, Sec24, doubles as a sensor of folded cargo and, upon cargo binding, acts as a guanine nucleotide exchange factor to activate the signaling protein Gα12 at the ER exit sites (ERESs). This step, in turn, activates a complex signaling network that activates and coordinates the ER export machinery and attenuates proteins synthesis, thus preventing large fluctuations of folded and potentially active cargo that could be harmful to the cell or the organism. We call this mechanism AREX (autoregulation of ER export) and expect that its identification will aid our understanding of human physiology and diseases that develop from secretory dysfunction.

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