Literature DB >> 16168372

Yos9 protein is essential for degradation of misfolded glycoproteins and may function as lectin in ERAD.

Reka Szathmary1, Regula Bielmann, Mihai Nita-Lazar, Patricie Burda, Claude A Jakob.   

Abstract

The Htm1/EDEM protein has been proposed to act as a "degradation lectin" for endoplasmic reticulum-associated degradation (ERAD) of misfolded glycoproteins. In this study, we provide genetic and biochemical evidence that Yos9 protein in Saccharomyces cerevisiae is essential for efficient degradation of mutant glycoproteins. Yos9 is a member of the OS-9 protein family, which is conserved among eukaryotes and shows similarities with mannose-6-phosphate receptors (MPRs). We found that amino acids conserved among OS-9 family members and MPRs were essential for Yos9 protein function. Immunoprecipitation showed that Yos9 specifically associated with misfolded carboxypeptidase Y (CPY*), an ERAD substrate, but only when it carried Man8GlcNAc2 or Man5GlcNAc2 N-glycans. Our experiments further suggested that Yos9 acts in the same pathway as Htm1/EDEM. Yos9 protein is important for glycoprotein degradation and may act via its MRH domain as a degradation lectin-like protein in the glycoprotein degradation pathway.

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Year:  2005        PMID: 16168372     DOI: 10.1016/j.molcel.2005.08.015

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  78 in total

Review 1.  GRP94: An HSP90-like protein specialized for protein folding and quality control in the endoplasmic reticulum.

Authors:  Michal Marzec; Davide Eletto; Yair Argon
Journal:  Biochim Biophys Acta       Date:  2011-11-03

2.  Structural and biochemical basis of Yos9 protein dimerization and possible contribution to self-association of 3-hydroxy-3-methylglutaryl-coenzyme A reductase degradation ubiquitin-ligase complex.

Authors:  Jennifer Hanna; Anja Schütz; Franziska Zimmermann; Joachim Behlke; Thomas Sommer; Udo Heinemann
Journal:  J Biol Chem       Date:  2012-01-18       Impact factor: 5.157

3.  OS9 Protein Interacts with Na-K-2Cl Co-transporter (NKCC2) and Targets Its Immature Form for the Endoplasmic Reticulum-associated Degradation Pathway.

Authors:  Elie Seaayfan; Nadia Defontaine; Sylvie Demaretz; Nancy Zaarour; Kamel Laghmani
Journal:  J Biol Chem       Date:  2015-12-31       Impact factor: 5.157

Review 4.  Ubiquitin ligases, critical mediators of endoplasmic reticulum-associated degradation.

Authors:  Zlatka Kostova; Yien Che Tsai; Allan M Weissman
Journal:  Semin Cell Dev Biol       Date:  2007-09-08       Impact factor: 7.727

Review 5.  The recognition and retrotranslocation of misfolded proteins from the endoplasmic reticulum.

Authors:  Kunio Nakatsukasa; Jeffrey L Brodsky
Journal:  Traffic       Date:  2008-02-24       Impact factor: 6.215

6.  Inhibition of p97-dependent protein degradation by Eeyarestatin I.

Authors:  Qiuyan Wang; Lianyun Li; Yihong Ye
Journal:  J Biol Chem       Date:  2008-01-16       Impact factor: 5.157

7.  Adapter-mediated substrate selection for endoplasmic reticulum-associated degradation.

Authors:  Kathleen Corcoran; Xiaoli Wang; Lonnie Lybarger
Journal:  J Biol Chem       Date:  2009-04-14       Impact factor: 5.157

8.  The ER-associated degradation component Der1p and its homolog Dfm1p are contained in complexes with distinct cofactors of the ATPase Cdc48p.

Authors:  Veit Goder; Pedro Carvalho; Tom A Rapoport
Journal:  FEBS Lett       Date:  2008-04-11       Impact factor: 4.124

9.  Htm1p-Pdi1p is a folding-sensitive mannosidase that marks N-glycoproteins for ER-associated protein degradation.

Authors:  Yi-Chang Liu; Danica Galonić Fujimori; Jonathan S Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  2016-06-28       Impact factor: 11.205

10.  Redundant and Antagonistic Roles of XTP3B and OS9 in Decoding Glycan and Non-glycan Degrons in ER-Associated Degradation.

Authors:  Annemieke T van der Goot; Margaret M P Pearce; Dara E Leto; Thomas A Shaler; Ron R Kopito
Journal:  Mol Cell       Date:  2018-04-26       Impact factor: 17.970

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