Literature DB >> 8475059

Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.

M Rogers1, F Yehiely, M Scott, S B Prusiner.   

Abstract

The only known component of the infectious prion is a posttranslationally modified protein known as the scrapie isoform of the prion protein, PrPSc. Upon limited proteolysis, a protease-resistant fragment designated PrP 27-30 is formed. Using in vitro mutagenesis, we examined the role of the N and C termini in the formation of PrPSc in persistently infected, mouse neuroblastoma (ScN2a) cells. Neither deletion of amino acids 23-88, which are also removed by proteinase K in the formation of PrP 27-30, nor deletion of the five octapeptide repeats within this region altered synthesis of PrPSc. Elongation of PrP with one, two, four, or six octapeptide repeats in addition to the five found in wild-type PrP did not alter the synthesis of PrPSc. Truncation of the C terminus was accomplished by substituting a translation stop codon for the predicted glycosylinositol phospholipid (GPI) anchor-attachment signal corresponding to amino acids 231-254. Expression of this C-terminal PrP mutant in ScN2a cells produced PrPSc that appeared to lack a GPI anchor. We conclude that neither the GPI anchor nor the N-terminal 66 amino acids are required for the synthesis of PrPSc as measured by the acquisition of limited resistance to proteinase K digestion. Whether these truncated or elongated PrP molecules are competent to participate in the formation of infectious prions remains to be established.

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Year:  1993        PMID: 8475059      PMCID: PMC46263          DOI: 10.1073/pnas.90.8.3182

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

1.  Deletion in prion protein gene in a Moroccan family.

Authors:  J L Laplanche; J Chatelain; J M Launay; C Gazengel; M Vidaud
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

2.  Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation.

Authors:  A Taraboulos; M Rogers; D R Borchelt; M P McKinley; M Scott; D Serban; S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

3.  Prion protein gene expression in cultured cells.

Authors:  M R Scott; D A Butler; D E Bredesen; M Wälchli; K K Hsiao; S B Prusiner
Journal:  Protein Eng       Date:  1988-04

4.  An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease.

Authors:  F Owen; M Poulter; T Shah; J Collinge; R Lofthouse; H Baker; R Ridley; J McVey; T J Crow
Journal:  Brain Res Mol Brain Res       Date:  1990-04

5.  Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

Authors:  M Scott; D Foster; C Mirenda; D Serban; F Coufal; M Wälchli; M Torchia; D Groth; G Carlson; S J DeArmond; D Westaway; S B Prusiner
Journal:  Cell       Date:  1989-12-01       Impact factor: 41.582

6.  Spontaneous neurodegeneration in transgenic mice with mutant prion protein.

Authors:  K K Hsiao; M Scott; D Foster; D F Groth; S J DeArmond; S B Prusiner
Journal:  Science       Date:  1990-12-14       Impact factor: 47.728

7.  Prion dementia without characteristic pathology.

Authors:  J Collinge; F Owen; M Poulter; M Leach; T J Crow; M N Rossor; J Hardy; M J Mullan; I Janota; P L Lantos
Journal:  Lancet       Date:  1990-07-07       Impact factor: 79.321

8.  Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

Authors:  S B Prusiner; M Scott; D Foster; K M Pan; D Groth; C Mirenda; M Torchia; S L Yang; D Serban; G A Carlson
Journal:  Cell       Date:  1990-11-16       Impact factor: 41.582

9.  Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.

Authors:  A Taraboulos; D Serban; S B Prusiner
Journal:  J Cell Biol       Date:  1990-06       Impact factor: 10.539

10.  Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.

Authors:  D R Borchelt; M Scott; A Taraboulos; N Stahl; S B Prusiner
Journal:  J Cell Biol       Date:  1990-03       Impact factor: 10.539

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  50 in total

1.  Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state.

Authors:  M Horiuchi; B Caughey
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

2.  Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein.

Authors:  L Zulianello; K Kaneko; M Scott; S Erpel; D Han; F E Cohen; S B Prusiner
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

3.  Glycosylation influences cross-species formation of protease-resistant prion protein.

Authors:  S A Priola; V A Lawson
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

4.  Spontaneous generation of anchorless prions in transgenic mice.

Authors:  Jan Stöhr; Joel C Watts; Giuseppe Legname; Abby Oehler; Azucena Lemus; Hoang-Oanh B Nguyen; Joshua Sussman; Holger Wille; Stephen J DeArmond; Stanley B Prusiner; Kurt Giles
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-12       Impact factor: 11.205

5.  Distance of sequons to the C-terminus influences the cellular N-glycosylation of the prion protein.

Authors:  Adrian R Walmsley; Nigel M Hooper
Journal:  Biochem J       Date:  2003-02-15       Impact factor: 3.857

6.  Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain.

Authors:  S Capellari; P Parchi; C M Russo; J Sanford; M S Sy; P Gambetti; R B Petersen
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

7.  From conversion to aggregation: protofibril formation of the prion protein.

Authors:  Mari L DeMarco; Valerie Daggett
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-24       Impact factor: 11.205

8.  Direct evidence of generation and accumulation of β-sheet-rich prion protein in scrapie-infected neuroblastoma cells with human IgG1 antibody specific for β-form prion protein.

Authors:  Toshiya Kubota; Yuta Hamazoe; Shuhei Hashiguchi; Daisuke Ishibashi; Kazuyuki Akasaka; Noriyuki Nishida; Shigeru Katamine; Suehiro Sakaguchi; Ryota Kuroki; Toshihiro Nakashima; Kazuhisa Sugimura
Journal:  J Biol Chem       Date:  2012-02-22       Impact factor: 5.157

9.  Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein.

Authors:  R A Williamson; D Peretz; N Smorodinsky; R Bastidas; H Serban; I Mehlhorn; S J DeArmond; S B Prusiner; D R Burton
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-09       Impact factor: 11.205

Review 10.  Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.

Authors:  Julie A Moreno; Glenn C Telling
Journal:  Methods Mol Biol       Date:  2017
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