Literature DB >> 19325625

The ubiquitylation machinery of the endoplasmic reticulum.

Christian Hirsch1, Robert Gauss, Sabine C Horn, Oliver Neuber, Thomas Sommer.   

Abstract

As proteins travel through the endoplasmic reticulum (ER), a quality-control system retains newly synthesized polypeptides and supports their maturation. Only properly folded proteins are released to their designated destinations. Proteins that cannot mature are left to accumulate, impairing the function of the ER. To maintain homeostasis, the protein-quality-control system singles out aberrant polypeptides and delivers them to the cytosol, where they are destroyed by the proteasome. The importance of this pathway is evident from the growing list of pathologies associated with quality-control defects in the ER.

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Year:  2009        PMID: 19325625     DOI: 10.1038/nature07962

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  99 in total

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2.  Membrane-bound Ubx2 recruits Cdc48 to ubiquitin ligases and their substrates to ensure efficient ER-associated protein degradation.

Authors:  Christian Schuberth; Alexander Buchberger
Journal:  Nat Cell Biol       Date:  2005-09-18       Impact factor: 28.824

3.  A complex of Yos9p and the HRD ligase integrates endoplasmic reticulum quality control into the degradation machinery.

Authors:  Robert Gauss; Ernst Jarosch; Thomas Sommer; Christian Hirsch
Journal:  Nat Cell Biol       Date:  2006-07-16       Impact factor: 28.824

4.  An adaptable standard for protein export from the endoplasmic reticulum.

Authors:  R Luke Wiseman; Evan T Powers; Joel N Buxbaum; Jeffery W Kelly; William E Balch
Journal:  Cell       Date:  2007-11-16       Impact factor: 41.582

Review 5.  Glycoprotein folding and the role of EDEM1, EDEM2 and EDEM3 in degradation of folding-defective glycoproteins.

Authors:  Silvia Olivari; Maurizio Molinari
Journal:  FEBS Lett       Date:  2007-05-04       Impact factor: 4.124

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Journal:  Nature       Date:  1996-12-05       Impact factor: 49.962

7.  The tumor autocrine motility factor receptor, gp78, is a ubiquitin protein ligase implicated in degradation from the endoplasmic reticulum.

Authors:  S Fang; M Ferrone; C Yang; J P Jensen; S Tiwari; A M Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-27       Impact factor: 11.205

8.  Human HRD1 is an E3 ubiquitin ligase involved in degradation of proteins from the endoplasmic reticulum.

Authors:  Marjolein Kikkert; Ram Doolman; Min Dai; Rachel Avner; Gerco Hassink; Sjaak van Voorden; Swapna Thanedar; Joseph Roitelman; Vincent Chau; Emmanuel Wiertz
Journal:  J Biol Chem       Date:  2003-10-30       Impact factor: 5.157

9.  PNG1, a yeast gene encoding a highly conserved peptide:N-glycanase.

Authors:  T Suzuki; H Park; N M Hollingsworth; R Sternglanz; W J Lennarz
Journal:  J Cell Biol       Date:  2000-05-29       Impact factor: 10.539

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Journal:  Mol Cell       Date:  2008-12-26       Impact factor: 17.970

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  166 in total

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Authors:  Qiuyan Wang; Yanfen Liu; Nia Soetandyo; Kheewoong Baek; Ramanujan Hegde; Yihong Ye
Journal:  Mol Cell       Date:  2011-06-24       Impact factor: 17.970

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

Review 3.  The delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiology.

Authors:  Christopher J Guerriero; Jeffrey L Brodsky
Journal:  Physiol Rev       Date:  2012-04       Impact factor: 37.312

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Journal:  Nat Cell Biol       Date:  2011-09-25       Impact factor: 28.824

Review 5.  Ubiquitin on the move: the ubiquitin modification system plays diverse roles in the regulation of endoplasmic reticulum- and plasma membrane-localized proteins.

Authors:  Damian D Guerra; Judy Callis
Journal:  Plant Physiol       Date:  2012-06-22       Impact factor: 8.340

6.  Type I transglutaminase accumulation in the endoplasmic reticulum may be an underlying cause of autosomal recessive congenital ichthyosis.

Authors:  Haibing Jiang; Ralph Jans; Wen Xu; Ellen A Rorke; Chen-Yong Lin; Ya-Wen Chen; Shengyun Fang; Yongwang Zhong; Richard L Eckert
Journal:  J Biol Chem       Date:  2010-07-27       Impact factor: 5.157

7.  J domain co-chaperone specificity defines the role of BiP during protein translocation.

Authors:  Shruthi S Vembar; Martin C Jonikas; Linda M Hendershot; Jonathan S Weissman; Jeffrey L Brodsky
Journal:  J Biol Chem       Date:  2010-04-29       Impact factor: 5.157

8.  Hepatic gene networks in morbidly obese patients with nonalcoholic fatty liver disease.

Authors:  Samer Gawrieh; Tesfaye M Baye; Melanie Carless; James Wallace; Richard Komorowski; David E Kleiner; Deborah Andris; Bassem Makladi; Regina Cole; Michael Charlton; Joanne Curran; Thomas D Dyer; Jac Charlesworth; Russell Wilke; John Blangero; Ahmed H Kissebah; Michael Olivier
Journal:  Obes Surg       Date:  2010-12       Impact factor: 4.129

Review 9.  Molecular pathogenesis of infections caused by Legionella pneumophila.

Authors:  Hayley J Newton; Desmond K Y Ang; Ian R van Driel; Elizabeth L Hartland
Journal:  Clin Microbiol Rev       Date:  2010-04       Impact factor: 26.132

10.  The UBX protein SAKS1 negatively regulates endoplasmic reticulum-associated degradation and p97-dependent degradation.

Authors:  David P LaLonde; Anthony Bretscher
Journal:  J Biol Chem       Date:  2010-12-06       Impact factor: 5.157

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