Literature DB >> 15112051

Role of N-linked polymannose oligosaccharides in targeting glycoproteins for endoplasmic reticulum-associated degradation.

R G Spiro1.   

Abstract

Misfolded or incompletely assembled multisubunit glycoproteins undergo endoplasmic reticulum-associated degradation (ERAD) regulated in large measure by their N-linked polymannose oligosaccharides. In this quality control system lectin interaction with Glc(3)Man(9)GlcNAc(2) glycans after trimming with endoplasmic reticulum (ER) alpha-glucosidases and alpha-mannosidases sorts out persistently unfolded glycoproteins for N-deglycosylation and proteolytic degradation. Monoglucosylated (Glc(1)Man(9)GlcNAc(2)) glycoproteins take part in the calnexin/calreticulin glucosylation-deglucosylation cycle, while the Man(8)GlcNAc(2) isomer B product of ER mannosidase I interacts with EDEM. Proteasomal degradation requires retrotranslocation into the cytosol through a Sec61 channel and deglycosylation by peptide: N-glycosidase (PNGase); in alternate models both PNGase and proteasomes may be either free in the cytosol or ER membrane-imbedded/attached. Numerous proteins appear to undergo nonproteasomal degradation in which deglycosylation and proteolysis take place in the ER lumen. The released free oligosaccharides (OS) are transported to the cytosol as OS-GlcNAc(2) along with similar components produced by the hydrolytic action of the oligosaccharyltransferase, where they together with OS from the proteasomal pathway are trimmed to Man(5)GlcNAc(1) by the action of cytosolic endo-beta- N-acetylglucosaminidase and alpha-mannosidase before entering the lysosomes. Some misfolded glycoproteins can recycle between the ER, intermediate and Golgi compartments, where they are further processed before ERAD. Moreover, properly folded glycoproteins with mannose-trimmed glycans can be deglucosylated in the Golgi by endomannosidase, thereby releasing calreticulin and permitting formation of complex OS. A number of regulatory controls have been described, including the glucosidase-glucosyltransferase shuttle, which controls the level of Glc(3)Man(9)GlcNAc(2)-P-P-Dol, and the unfolded protein response, which enhances synthesis of components of the quality control system.

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Year:  2004        PMID: 15112051     DOI: 10.1007/s00018-004-4037-8

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  32 in total

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Review 3.  Free N-linked oligosaccharide chains: formation and degradation.

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4.  Novel mannosidase inhibitors probe glycoprotein degradation pathways in cells.

Authors:  Terry D Butters; Dominic S Alonzi; Nikolay V Kukushkin; Yuan Ren; Yves Blériot
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5.  Synthesis of fluorine substituted oligosaccharide analogues of monoglucosylated glycan chain, a proposed ligand of lectin-chaperone calreticulin and calnexin.

Authors:  Yukishige Ito; Shinya Hagihara; Midori A Arai; Ichiro Matsuo; Maki Takatani
Journal:  Glycoconj J       Date:  2004       Impact factor: 2.916

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8.  Identification of roles for peptide: N-glycanase and endo-beta-N-acetylglucosaminidase (Engase1p) during protein N-glycosylation in human HepG2 cells.

Authors:  Isabelle Chantret; Magali Fasseu; Karim Zaoui; Christiane Le Bizec; Hassane Sadou Yayé; Thierry Dupré; Stuart E H Moore
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9.  Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.

Authors:  Markus Damme; Willy Morelle; Bernhard Schmidt; Claes Andersson; Jens Fogh; Jean-Claude Michalski; Torben Lübke
Journal:  Mol Cell Biol       Date:  2010-01       Impact factor: 4.272

10.  A complex between peptide:N-glycanase and two proteasome-linked proteins suggests a mechanism for the degradation of misfolded glycoproteins.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-09       Impact factor: 11.205

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