Literature DB >> 10390615

Retrograde protein translocation: ERADication of secretory proteins in health and disease.

R K Plemper1, D H Wolf.   

Abstract

Eukaryotic cells have a complex degradation machinery that eliminates misfolded or unassembled secretory proteins from the endoplasmic reticulum (ER). The proteins are retained in an ER/pre-Golgi compartment and then hydrolysed by the cytosolic ubiquitin-proteasome system. This requires retrograde translocation of proteins from the ER back to the cytoplasm, which is mediated by Sec61, the central component of the ER protein-import channel. This proteolytic pathway prevents a potentially lethal aggregation of secretory proteins; however, several viruses misuse it to escape detection, and bacterial and plant toxins might also exploit it. Underactive or overactive ER degradation machinery contributes to the pathogenesis of several severe human diseases.

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Year:  1999        PMID: 10390615     DOI: 10.1016/s0968-0004(99)01420-6

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  90 in total

1.  Identification of discrete classes of endosome-derived small vesicles as a major cellular pool for recycling membrane proteins.

Authors:  S N Lim; F Bonzelius; S H Low; H Wille; T Weimbs; G A Herman
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

Review 2.  Aggresomes and Russell bodies. Symptoms of cellular indigestion?

Authors:  R R Kopito; R Sitia
Journal:  EMBO Rep       Date:  2000-09       Impact factor: 8.807

3.  Cellular internalization of cytolethal distending toxin from Haemophilus ducreyi.

Authors:  X Cortes-Bratti; E Chaves-Olarte; T Lagergård; M Thelestam
Journal:  Infect Immun       Date:  2000-12       Impact factor: 3.441

Review 4.  Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders.

Authors:  N Gregersen; P Bross; M M Jørgensen; T J Corydon; B S Andresen
Journal:  J Inherit Metab Dis       Date:  2000-07       Impact factor: 4.982

5.  A protein-protein interaction map of the Caenorhabditis elegans 26S proteasome.

Authors:  A Davy; P Bello; N Thierry-Mieg; P Vaglio; J Hitti; L Doucette-Stamm; D Thierry-Mieg; J Reboul; S Boulton; A J Walhout; O Coux; M Vidal
Journal:  EMBO Rep       Date:  2001-09       Impact factor: 8.807

6.  Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation.

Authors:  J Ma; S Lindquist
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-11       Impact factor: 11.205

7.  Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein.

Authors:  Y Yedidia; L Horonchik; S Tzaban; A Yanai; A Taraboulos
Journal:  EMBO J       Date:  2001-10-01       Impact factor: 11.598

8.  Toward development of a screen to identify randomly encoded, foldable sequences.

Authors:  Yoshihisa Hagihara; Peter S Kim
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-07       Impact factor: 11.205

Review 9.  Lessons from viral manipulation of protein disposal pathways.

Authors:  Margo H Furman; Hidde L Ploegh
Journal:  J Clin Invest       Date:  2002-10       Impact factor: 14.808

Review 10.  T-cell control by human T-cell leukemia/lymphoma virus type 1.

Authors:  Genoveffa Franchini; Risaku Fukumoto; Jake R Fullen
Journal:  Int J Hematol       Date:  2003-11       Impact factor: 2.490

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