Cargo selection and export from the endoplasmic reticulum is mediated by the COPII coat machinery that includes the small GTPase Sar1 and the Sec23/24 and Sec13/31 complexes. We have analyzed the sequential events regulated by purified Sar1 and COPII coat complexes during synchronized export of cargo from the ER in vitro. We find that activation of Sar1 alone, in the absence of other cytosolic components, leads to the formation of ER-derived tubular domains that resemble ER transitional elements that initiate cargo selection. These Sar1-generated tubular domains were shown to be transient, functional intermediates in ER to Golgi transport in vitro. By following cargo export in live cells, we show that ER export in vivo is also characterized by the formation of dynamic tubular structures. Our results demonstrate an unanticipated and novel role for Sar1 in linking cargo selection with ER morphogenesis through the generation of transitional tubular ER export sites.
The Sar1 Gtpase Coordinates Biosynthetic Cargo Selection with Endoplasmic Reticulum Export Site Assembly
The online version of this article contains supplemental material.
Dr. Aridor's current address is Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, 3500 Terrace Street, BST South 362, Pittsburgh, PA 15251.
Abbreviations used in this paper: BIP, immunoglobulin binding protein; DIC, differential interference contrast; DTSSP, 3′-dithiobissulfosuccimidylpropionate; GFP, green fluorescent protein; GST, glutathione-S-transferase; Man II, 1,2-mannosidase II; MT, microtubule; NRK, normal rat kidney; VTC, vesicular tubular cluster.
Meir Aridor, Kenneth N. Fish, Sergei Bannykh, Jacques Weissman, Theresa H. Roberts, Jennifer Lippincott-Schwartz, William E. Balch; The Sar1 Gtpase Coordinates Biosynthetic Cargo Selection with Endoplasmic Reticulum Export Site Assembly. J Cell Biol 8 January 2001; 152 (1): 213–230. doi: https://doi.org/10.1083/jcb.152.1.213
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