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PMID: 10995433 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Exclusion of golgi residents from transport vesicles budding from Golgi cisternae in intact cells.

The Journal of cell biology ·Vol. 150 ·No. 6 ·2000-09-18 ·Pages 1263-70

Orci L, Amherdt M, Ravazzola M, Perrelet A, Rothman JE

Abstract

A central feature of cisternal progression/maturation models for anterograde transport across the Golgi stack is the requirement that the entire population of steady-state residents of this organelle be continuously transported backward to earlier cisternae to avoid loss of these residents as the membrane of the oldest (trans-most) cisterna departs the stack. For this to occur, resident proteins must be packaged into retrograde-directed transport vesicles, and to occur at the rate of anterograde transport, resident proteins must be present in vesicles at a higher concentration than in cisternal membranes. We have tested this prediction by localizing two steady-state residents of medial Golgi cisternae (mannosidase II and N-acetylglucosaminyl transferase I) at the electron microscopic level in intact cells. In both cases, these abundant cisternal constituents were strongly excluded from buds and vesicles. This result suggests that cisternal progression takes place substantially more slowly than most protein transport and therefore is unlikely to be the predominant mechanism of anterograde movement.

MeSH Terms
Arabidopsis Proteins Carrier Proteins/metabolism Cytoplasmic Granules/enzymology,ultrastructure Golgi Apparatus/enzymology,ultrastructure HeLa Cells Humans Immunohistochemistry Intracellular Membranes/enzymology,ultrastructure Islets of Langerhans/metabolism,ultrastructure Mannosidases/metabolism Microscopy, Immunoelectron N-Acetylglucosaminyltransferases/metabolism Plant Proteins/metabolism Ubiquitin-Protein Ligases
Chemicals
Arabidopsis Proteins Carrier Proteins Plant Proteins AT2G32950 protein, Arabidopsis Ubiquitin-Protein Ligases N-Acetylglucosaminyltransferases alpha-1,3-mannosyl-glycoprotein beta-1,2-N-acetylglucosaminyltransferase I Mannosidases mannosyl-oligosaccharide 1,3 - 1,6-alpha-mannosidase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Orci L
Department of Morphology, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
Amherdt M
Ravazzola M
Perrelet A
Rothman J E
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
2000-09-18
Pages
1263-70
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2150693
Subset
IM
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