Literature DB >> 10597633

ER protein quality control and proteasome-mediated protein degradation.

J L Brodsky1, A A McCracken.   

Abstract

A variety of mutant polypeptides that are associated with human disease are targeted for degradation by an endoplasmic reticulum (ER) quality control system. In addition, physiological signals and viral gene products can target the degradation of several ER resident proteins and secreted proteins passing through the ER. Although the mechanism of protein quality control and the site of degradation were obscure, recent data indicate that degradation requires the cytosolic proteasome. Biochemical and genetic analyses have indicated that both lumenal and integral membrane proteins are selected for proteolysis and exported to the cytosol by a process that in several cases requires ER associated molecular chaperones.

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Year:  1999        PMID: 10597633     DOI: 10.1006/scdb.1999.0321

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  96 in total

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Review 7.  Lessons from viral manipulation of protein disposal pathways.

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Review 8.  Progress in focus: recent advances in histochemistry and cell biology.

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9.  Assembly, secretion, and vacuolar delivery of a hybrid immunoglobulin in plants.

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10.  Hsp70 molecular chaperone facilitates endoplasmic reticulum-associated protein degradation of cystic fibrosis transmembrane conductance regulator in yeast.

Authors:  Y Zhang; G Nijbroek; M L Sullivan; A A McCracken; S C Watkins; S Michaelis; J L Brodsky
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