Literature DB >> 8294506

Characterization of the budding compartment of mouse hepatitis virus: evidence that transport from the RER to the Golgi complex requires only one vesicular transport step.

J Krijnse-Locker1, M Ericsson, P J Rottier, G Griffiths.   

Abstract

Mouse hepatitis coronavirus (MHV) buds into pleomorphic membrane structures with features expected of the intermediate compartment between the ER and the Golgi complex. Here, we characterize the MHV budding compartment in more detail in mouse L cells using streptolysin O (SLO) permeabilization which allowed us to better visualize the membrane structures at the ER-Golgi boundary. The MHV budding compartment shares membrane continuities with the rough ER as well as with cisternal elements on one side of the Golgi stack. It also labeled with p58 and rab2, two markers of the intermediate compartment, and with PDI, usually considered to be a marker of the rough ER. The membranes of the budding compartment, as well as the budding virions themselves, but not the rough ER, labeled with the N-acetyl-galactosamine (GalNAc)-specific lectin Helix pomatia. When the SLO-permeabilized cells were treated with guanosine 5'-(3-O-thio)triphosphate (GTP gamma S), the budding compartment accumulated a large number of beta-cop-containing buds and vesicular profiles. Complementary biochemical experiments were carried out to determine whether vesicular transport was required for the newly synthesized M protein, that contains only O-linked oligosaccharides, to acquire first, GalNAc and second, the Golgi modifications galactose and sialic acid. The results from both in vivo studies and from the use of SLO-permeabilized cells showed that, while GalNAc addition occurred under conditions which block vesicular transport, both cytosol and ATP were prerequisites for the M protein oligosaccharides to acquire Golgi modifications. Collectively, our data argue that transport from the rough ER to the Golgi complex requires only one vesicular transport step and that the intermediate compartment is a specialized domain of the endoplasmatic reticulum that extends to the first cisterna on the cis side of the Golgi stack.

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Year:  1994        PMID: 8294506      PMCID: PMC2119890          DOI: 10.1083/jcb.124.1.55

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  53 in total

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Authors:  J D Lindsey; M H Ellisman
Journal:  J Neurosci       Date:  1985-12       Impact factor: 6.167

4.  Beta-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the Golgi complex, shows homology to beta-adaptin.

Authors:  R Duden; G Griffiths; R Frank; P Argos; T E Kreis
Journal:  Cell       Date:  1991-02-08       Impact factor: 41.582

5.  SEC21 is a gene required for ER to Golgi protein transport that encodes a subunit of a yeast coatomer.

Authors:  M Hosobuchi; T Kreis; R Schekman
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6.  Localization of binding sites for concanavalin A, Ricinus communis I and Helix pomatia lectin in the Golgi apparatus of rat small intestinal absorptive cells.

Authors:  M Pavelka; A Ellinger
Journal:  J Histochem Cytochem       Date:  1985-09       Impact factor: 2.479

7.  Calcium and GTP: essential components in vesicular trafficking between the endoplasmic reticulum and Golgi apparatus.

Authors:  C J Beckers; W E Balch
Journal:  J Cell Biol       Date:  1989-04       Impact factor: 10.539

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Authors:  J A Den Boon; E J Snijder; J K Locker; M C Horzinek; P J Rottier
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Authors:  J Roth
Journal:  J Cell Biol       Date:  1984-02       Impact factor: 10.539

Review 10.  The Golgi complex: in vitro veritas?

Authors:  I Mellman; K Simons
Journal:  Cell       Date:  1992-03-06       Impact factor: 41.582

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  158 in total

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Review 7.  The molecular biology of coronaviruses.

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9.  Ribonucleocapsid formation of severe acute respiratory syndrome coronavirus through molecular action of the N-terminal domain of N protein.

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