Abstract
The transfer of the vesicular stomatitis virus-encoded glycoprotein (G protein) between Golgi populations in fused cells (Rothman, J. E., L. J. Urbani, and R. Brands. 1984. J. Cell Biol. 99:248-259) is exploited here to study and to help define the compartmental organization of the Golgi stack and to characterize the mechanism of intercompartmental transport. We find that G protein that has just received its peripheral N-acetylglucosamine in the Golgi complex of one cell is efficiently transferred to the Golgi complex of another cell to receive galactose (Gal). Remarkably, this transport occurs at the same rate between these two compartments whether they are present in the same or different Golgi populations. Therefore, a dissociative (presumably vesicular) transport step moves G protein from one part of the Golgi in which N-acetylglucosamine is added to another in which Gal is added. Minutes later, upon receiving Gal, the same G protein molecules are very poorly transferred to an exogenous Golgi population after cell fusion. Therefore, once this intercompartmental transfer has already taken place (before fusion), it cannot take place again (after fusion); i.e., transport across the compartment boundary in the Golgi complex that separates the sites of N-acetylglucosamine and Gal incorporation is a vectorial process. We conclude that transfers between Golgi cisternae occur by a stochastic process in which transport vesicles budding from cisternae dissociate, can diffuse away, and then attach to and fuse with the appropriate target cisterna residing in the same or in a different stack, based on a biochemical pairing after a random encounter. Under these circumstances, a transported protein would almost always randomize among stacks with each intercisternal transfer; it would not progress systematically through a single stack. Altogether, our studies define three sequential compartments in the Golgi stack.
MeSH Terms
Acetylglucosamine/metabolism
Ammonium Chloride/pharmacology
Animals
Cell Compartmentation
Cell Fusion
Cell Line
Cricetinae
Cricetulus
Cycloheximide/pharmacology
Female
Glucosamine/metabolism
Golgi Apparatus/metabolism
Kinetics
Lectins/metabolism
Membrane Glycoproteins
Membrane Proteins/metabolism
Ovary/ultrastructure
Plant Lectins
Viral Envelope Proteins
Viral Proteins/metabolism
Chemicals
G protein, vesicular stomatitis virus
Lectins
Membrane Glycoproteins
Membrane Proteins
Plant Lectins
Ricinus communis agglutinin-1
Viral Envelope Proteins
Viral Proteins
Ammonium Chloride
Cycloheximide
Glucosamine
Acetylglucosamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rothman J E
Miller R L
Urbani L J
References (26)
26 references, click to expand
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
Nature. 1970 Aug 15;227(5259):680-5
PMID: 5432063
-
Intracellular aspects of the process of protein synthesis.
Science. 1975 Aug 1;189(4200):347-58
PMID: 1096303
-
Isolation of wheat germ agglutinin-resistant clones of Chinese hamster ovary cells deficient in membrane sialic acid and galactose.
J Biol Chem. 1977 Feb 10;252(3):1107-16
PMID: 320201
-
Oligosaccharide chains are trimmed during synthesis of the envelope glycoprotein of vesicular stomatitis virus.
Proc Natl Acad Sci U S A. 1978 Feb;75(2):754-8
PMID: 204932
-
Carbohydrate structure of vesicular stomatitis virus glycoprotein.
J Biol Chem. 1978 Aug 25;253(16):5600-12
PMID: 209045
-
Structure of the altered oligosaccharide present in glycoproteins from a clone of Chinese hamster ovary cells deficient in N-acetylglucosaminyltransferase activity.
J Biol Chem. 1978 Sep 25;253(18):6426-31
PMID: 681360
-
Structural determinants of Ricinus communis agglutinin and toxin specificity for oligosaccharides.
J Biol Chem. 1979 Oct 10;254(19):9795-9
PMID: 489569
-
The Golgi complex: crossroads for vesicular traffic.
Int Rev Exp Pathol. 1980;22:227-51
PMID: 7005145
-
The golgi apparatus: two organelles in tandem.
Science. 1981 Sep 11;213(4513):1212-9
PMID: 7268428
-
Synthesis and processing of asparagine-linked oligosaccharides.
Annu Rev Biochem. 1981;50:555-83
PMID: 7023366
-
Transient activity of Golgi-like membranes as donors of vesicular stomatitis viral glycoprotein in vitro.
J Cell Biol. 1981 Sep;90(3):697-704
PMID: 6270159
-
Diffusion of injected macromolecules within the cytoplasm of living cells.
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4407-10
PMID: 6945591
-
The Golgi apparatus (complex)-(1954-1981)-from artifact to center stage.
J Cell Biol. 1981 Dec;91(3 Pt 2):77s-103s
PMID: 7033246
-
Early and late functions associated with the Golgi apparatus reside in distinct compartments.
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7453-7
PMID: 6801652
-
Immunocytochemical localization of galactosyltransferase in HeLa cells: codistribution with thiamine pyrophosphatase in trans-Golgi cisternae.
J Cell Biol. 1982 Apr;93(1):223-9
PMID: 6121819
-
Purification and macromolecular properties of a sialic acid-specific lectin from the slug Limax flavus.
J Biol Chem. 1982 Jul 10;257(13):7574-80
PMID: 7085639
-
Viral membrane proteins acquire galactose in trans Golgi cisternae during intracellular transport.
J Cell Biol. 1982 Dec;95(3):781-92
PMID: 6924936
-
Evidence for extensive subcellular organization of asparagine-linked oligosaccharide processing and lysosomal enzyme phosphorylation.
J Biol Chem. 1983 Mar 10;258(5):3159-65
PMID: 6402509
-
Dissection of the Golgi complex. I. Monensin inhibits the transport of viral membrane proteins from medial to trans Golgi cisternae in baby hamster kidney cells infected with Semliki Forest virus.
J Cell Biol. 1983 Mar;96(3):835-50
PMID: 6682112
-
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus.
J Cell Biol. 1983 Jul;97(1):270-5
PMID: 6223041
-
Immunoelectron microscopic exploration of the Golgi complex.
J Histochem Cytochem. 1983 Aug;31(8):1049-56
PMID: 6863900
-
Application of lectin--gold complexes for electron microscopic localization of glycoconjugates on thin sections.
J Histochem Cytochem. 1983 Aug;31(8):987-99
PMID: 6190857
-
Subfractionation of rat liver Golgi apparatus: separation of enzyme activities involved in the biosynthesis of the phosphomannosyl recognition marker in lysosomal enzymes.
Proc Natl Acad Sci U S A. 1983 Jul;80(13):3938-42
PMID: 6306653
-
Lectin-binding sites as markers of Golgi subcompartments: proximal-to-distal maturation of oligosaccharides.
J Cell Biol. 1983 Oct;97(4):1243-8
PMID: 6194163
-
Selection of lectin-resistant mutants of animal cells.
Methods Enzymol. 1983;96:157-84
PMID: 6656629
-
Transport of protein between cytoplasmic membranes of fused cells: correspondence to processes reconstituted in a cell-free system.
J Cell Biol. 1984 Jul;99(1 Pt 1):248-59
PMID: 6429157