Literature DB >> 8930893

Uptake and incorporation of an epitope-tagged sialic acid donor into intact rat liver Golgi compartments. Functional localization of sialyltransferase overlaps with beta-galactosyltransferase but not with sialic acid O-acetyltransferase.

R Chammas1, J M McCaffery, A Klein, Y Ito, L Saucan, G Palade, M G Farquhar, A Varki.   

Abstract

The transfer of sialic acids (Sia) from CMP-sialic acid (CMP-Sia) to N-linked sugar chains is thought to occur as a final step in their biosynthesis in the trans portion of the Golgi apparatus. In some cell types such Sia residues can have O-acetyl groups added to them. We demonstrate here that rat hepatocytes express 9-O-acetylated Sias mainly at the plasma membranes of both apical (bile canalicular) and basolateral (sinusoidal) domains. Golgi fractions also contain 9-O-acetylated Sias on similar N-linked glycoproteins, indicating that O-acetylation may take place in the Golgi. We show here that CMP-Sia-FITC (with a fluorescein group attached to the Sia) is taken up by isolated intact Golgi compartments. In these preparations, Sia-FITC is transferred to endogenous glycoprotein acceptors and can be immunochemically detected in situ. Addition of unlabeled UDP-Gal enhances Sia-FITC incorporation, indicating a substantial overlap of beta-galactosyltransferase and sialyltransferase machineries. Moreover, the same glycoproteins that incorporate Sia-FITC also accept [3H]galactose from the donor UDP-[3H]Gal. In contrast, we demonstrate with three different approaches (double-labeling, immunoelectron microscopy, and addition of a diffusible exogenous acceptor) that sialyltransferase and O-acetyltransferase machineries are much more separated from one another. Thus, 9-O-acetylation occurs after the last point of Sia addition in the trans-Golgi network. Indeed, we show that 9-O-acetylated sialoglycoproteins are preferentially segregated into a subset of vesicular carriers that concentrate membrane-bound, but not secretory, proteins.

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Year:  1996        PMID: 8930893      PMCID: PMC276019          DOI: 10.1091/mbc.7.11.1691

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  57 in total

1.  Attachment of terminal N-acetylglucosamine to asparagine-linked oligosaccharides occurs in central cisternae of the Golgi stack.

Authors:  W G Dunphy; R Brands; J E Rothman
Journal:  Cell       Date:  1985-02       Impact factor: 41.582

Review 2.  Compartmental organization of the Golgi stack.

Authors:  W G Dunphy; J E Rothman
Journal:  Cell       Date:  1985-08       Impact factor: 41.582

3.  O-acetylation of disialoganglioside GD3 by human melanoma cells creates a unique antigenic determinant.

Authors:  D A Cheresh; R A Reisfeld; A P Varki
Journal:  Science       Date:  1984-08-24       Impact factor: 47.728

4.  Evidence for extensive subcellular organization of asparagine-linked oligosaccharide processing and lysosomal enzyme phosphorylation.

Authors:  D E Goldberg; S Kornfeld
Journal:  J Biol Chem       Date:  1983-03-10       Impact factor: 5.157

5.  Sialylation of glycoprotein oligosaccharides with N-acetyl-, N-glycolyl-, and N-O-diacetylneuraminic acids.

Authors:  H H Higa; J C Paulson
Journal:  J Biol Chem       Date:  1985-07-25       Impact factor: 5.157

6.  Purification and characterization of a rat liver Golgi alpha-mannosidase capable of processing asparagine-linked oligosaccharides.

Authors:  I Tabas; S Kornfeld
Journal:  J Biol Chem       Date:  1979-11-25       Impact factor: 5.157

7.  Distribution of organelles and membranes between hepatocytes and nonhepatocytes in the rat liver parenchyma. A stereological study.

Authors:  A Blouin; R P Bolender; E R Weibel
Journal:  J Cell Biol       Date:  1977-02       Impact factor: 10.539

8.  Galactose transfer to endogenous acceptors within Golgi fractions of rat liver.

Authors:  J J Bergeron; R A Rachubinski; R A Sikstrom; B I Posner; J Paiement
Journal:  J Cell Biol       Date:  1982-01       Impact factor: 10.539

9.  An autosomal dominant gene regulates the extent of 9-O-acetylation of murine erythrocyte sialic acids. A probable explanation for the variation in capacity to activate the human alternate complement pathway.

Authors:  A Varki; S Kornfeld
Journal:  J Exp Med       Date:  1980-09-01       Impact factor: 14.307

10.  Dissection of the Golgi complex. II. Density separation of specific Golgi functions in virally infected cells treated with monensin.

Authors:  P Quinn; G Griffiths; G Warren
Journal:  J Cell Biol       Date:  1983-03       Impact factor: 10.539

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  4 in total

Review 1.  Harnessing cancer cell metabolism for theranostic applications using metabolic glycoengineering of sialic acid in breast cancer as a pioneering example.

Authors:  Haitham A Badr; Dina M M AlSadek; Motawa E El-Houseini; Christopher T Saeui; Mohit P Mathew; Kevin J Yarema; Hafiz Ahmed
Journal:  Biomaterials       Date:  2016-11-25       Impact factor: 12.479

2.  Enzymatic 4-O-acetylation of N-acetylneuraminic acid in guinea-pig liver.

Authors:  M Iwersen; V Vandamme-Feldhaus; R Schauer
Journal:  Glycoconj J       Date:  1998-09       Impact factor: 2.916

3.  Sialylation of beta1 integrins blocks cell adhesion to galectin-3 and protects cells against galectin-3-induced apoptosis.

Authors:  Ya Zhuo; Roger Chammas; Susan L Bellis
Journal:  J Biol Chem       Date:  2008-08-08       Impact factor: 5.157

Review 4.  Exploration of the Sialic Acid World.

Authors:  Roland Schauer; Johannis P Kamerling
Journal:  Adv Carbohydr Chem Biochem       Date:  2018-11-28       Impact factor: 12.200

  4 in total

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