Literature DB >> 15814429

Search and destroy: ER quality control and ER-associated protein degradation.

Ayaz Sayeed1, Davis T W Ng.   

Abstract

Proteins synthesized in the endoplasmic reticulum (ER) encounter quality control checkpoints that verify their fitness to proceed in the secretory pathway. Molecules undergoing folding and assembly are kept out of the exocytic pathway until maturation is complete. Misfolded side products that inevitably form are removed from the mixture of conformers and returned to the cytosol for degradation. How unfolded proteins are recognized and how irreversibly misfolded proteins are sorted to ER-associated degradation pathways was poorly understood. Recent developments from a combination of genetic and biochemical analyses has revealed new insights into these mechanisms. The emerging view shows distinct pathways working in collaboration to filter the diverse range of unfolded proteins from the transport flow and to divert misfolded molecules for destruction.

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Year:  2005        PMID: 15814429     DOI: 10.1080/10409230590918685

Source DB:  PubMed          Journal:  Crit Rev Biochem Mol Biol        ISSN: 1040-9238            Impact factor:   8.250


  32 in total

1.  Transmembrane segments prevent surface expression of sodium channel Nav1.8 and promote calnexin-dependent channel degradation.

Authors:  Qian Li; Yuan-Yuan Su; Hao Wang; Lei Li; Qiong Wang; Lan Bao
Journal:  J Biol Chem       Date:  2010-08-18       Impact factor: 5.157

2.  Intrinsic capacities of molecular sensors of the unfolded protein response to sense alternate forms of endoplasmic reticulum stress.

Authors:  Jenny B DuRose; Arvin B Tam; Maho Niwa
Journal:  Mol Biol Cell       Date:  2006-05-03       Impact factor: 4.138

3.  A bipartite trigger for dislocation directs the proteasomal degradation of an endoplasmic reticulum membrane glycoprotein.

Authors:  Vanessa M Noriega; Domenico Tortorella
Journal:  J Biol Chem       Date:  2007-12-17       Impact factor: 5.157

Review 4.  The protective and destructive roles played by molecular chaperones during ERAD (endoplasmic-reticulum-associated degradation).

Authors:  Jeffrey L Brodsky
Journal:  Biochem J       Date:  2007-06-15       Impact factor: 3.857

Review 5.  The activities and function of molecular chaperones in the endoplasmic reticulum.

Authors:  Teresa M Buck; Christine M Wright; Jeffrey L Brodsky
Journal:  Semin Cell Dev Biol       Date:  2007-09-08       Impact factor: 7.727

Review 6.  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

7.  Degradation of a cytosolic protein requires endoplasmic reticulum-associated degradation machinery.

Authors:  Meredith Boyle Metzger; Matthew J Maurer; Beverley M Dancy; Susan Michaelis
Journal:  J Biol Chem       Date:  2008-09-23       Impact factor: 5.157

8.  Degradation of sterol regulatory element-binding protein precursor requires the endoplasmic reticulum-associated degradation components Ubc7 and Hrd1 in fission yeast.

Authors:  Bridget T Hughes; Christine C Nwosu; Peter J Espenshade
Journal:  J Biol Chem       Date:  2009-06-11       Impact factor: 5.157

9.  Analysis of quality control substrates in distinct cellular compartments reveals a unique role for Rpn4p in tolerating misfolded membrane proteins.

Authors:  Meredith Boyle Metzger; Susan Michaelis
Journal:  Mol Biol Cell       Date:  2008-12-10       Impact factor: 4.138

10.  Cadmium-mediated rescue from ER-associated degradation induces expression of its exporter.

Authors:  David J Adle; Wenzhong Wei; Nathan Smith; Joshua J Bies; Jaekwon Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2009-06-10       Impact factor: 11.205

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