Literature DB >> 15571817

Endoplasmic reticulum-associated protein degradation--one model fits all?

Christian Hirsch1, Ernst Jarosch, Thomas Sommer, Dieter H Wolf.   

Abstract

The endoplasmic reticulum (ER) is the eukaryotic organelle where most secretory proteins are folded for subsequent delivery to their site of action. Proper folding of newly synthesized proteins is monitored by a stringent ER quality control system. This system recognizes misfolded or unassembled proteins and prevents them from reaching their final destination. Instead, they are extracted from the ER, polyubiquitinated and degraded by the cytosolic proteasome. With the identification of novel components and substrates, a more and more complex picture of this process emerges in which distinct pathways target different sets of substrates for destruction.

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Year:  2004        PMID: 15571817     DOI: 10.1016/j.bbamcr.2004.10.006

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  22 in total

1.  Newly discovered viral E3 ligase pK3 induces endoplasmic reticulum-associated degradation of class I major histocompatibility proteins and their membrane-bound chaperones.

Authors:  Roger A Herr; Xiaoli Wang; Joy Loh; Herbert W Virgin; Ted H Hansen
Journal:  J Biol Chem       Date:  2012-03-08       Impact factor: 5.157

2.  Membrane and soluble substrates of the Doa10 ubiquitin ligase are degraded by distinct pathways.

Authors:  Tommer Ravid; Stefan G Kreft; Mark Hochstrasser
Journal:  EMBO J       Date:  2006-01-26       Impact factor: 11.598

3.  The cytoplasmic Hsp70 chaperone machinery subjects misfolded and endoplasmic reticulum import-incompetent proteins to degradation via the ubiquitin-proteasome system.

Authors:  Sae-Hun Park; Natalia Bolender; Frederik Eisele; Zlatka Kostova; Junko Takeuchi; Philip Coffino; Dieter H Wolf
Journal:  Mol Biol Cell       Date:  2006-10-25       Impact factor: 4.138

4.  Aggregated myocilin induces russell bodies and causes apoptosis: implications for the pathogenesis of myocilin-caused primary open-angle glaucoma.

Authors:  Gary Hin-Fai Yam; Katarina Gaplovska-Kysela; Christian Zuber; Jürgen Roth
Journal:  Am J Pathol       Date:  2007-01       Impact factor: 4.307

Review 5.  The ubiquitin-proteasome system in myocardial ischaemia and preconditioning.

Authors:  Saul R Powell; Andras Divald
Journal:  Cardiovasc Res       Date:  2009-09-30       Impact factor: 10.787

6.  Lumenal peroxisomal protein aggregates are removed by concerted fission and autophagy events.

Authors:  Selvambigai Manivannan; Rinse de Boer; Marten Veenhuis; Ida J van der Klei
Journal:  Autophagy       Date:  2013-04-09       Impact factor: 16.016

Review 7.  Free N-linked oligosaccharide chains: formation and degradation.

Authors:  Tadashi Suzuki; Yoko Funakoshi
Journal:  Glycoconj J       Date:  2006-07       Impact factor: 2.916

8.  Upregulation of proteasome activity rescues cardiomyocytes following pulse treatment with a proteasome inhibitor.

Authors:  Ping Wang; Justine Calise; Keren Powell; Andras Divald; Saul R Powell
Journal:  Am J Cardiovasc Dis       Date:  2014-01-15

Review 9.  Role of ubiquitin-proteasome system (UPS) in left ventricular hypertrophy (LVH).

Authors:  Federico Cacciapuoti
Journal:  Am J Cardiovasc Dis       Date:  2014-01-15

10.  Sodium 4-phenylbutyrate ameliorates the effects of cataract-causing mutant gammaD-crystallin in cultured cells.

Authors:  Bo Gong; Li-Yun Zhang; Dennis Shun-Chiu Lam; Chi-Pui Pang; Gary Hin-Fai Yam
Journal:  Mol Vis       Date:  2010-06-04       Impact factor: 2.367

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