Literature DB >> 11709001

A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.

P K Panegyres1, K Toufexis, B A Kakulas, L Cernevakova, P Brown, B Ghetti, P Piccardo, S R Dlouhy.   

Abstract

BACKGROUND: Gerstmann-Sträussler-Scheinker disease is a rare form of prion disease.
OBJECTIVE: To determine the prion mutation in a 51-year-old man without a family history of neurologic disease who died from Gerstmann-Sträussler-Scheinker disease. PATIENT AND METHODS: The patient was a 51-year-old man who died after a 9-year illness characterized by dementia and eventually ataxia. Neuropathologic studies were performed, the results of which revealed abundant prion protein-immunopositive amyloid plaques in the cerebellum without spongiform degeneration.
RESULTS: Genetic analysis of the prion protein gene showed a novel mutation at codon 131 that caused a valine-for-glycine substitution (G131V) and homozygosity at codon 129 (129M). Proteinase K-resistant prion protein was detected by Western blot analysis.
CONCLUSIONS: This is the first mutation described in the short, antiparallel beta-sheet domain of the prion protein. This report highlights the importance of genetic analysis of patients with atypical dementia even in the absence of a family history.

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Year:  2001        PMID: 11709001     DOI: 10.1001/archneur.58.11.1899

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  23 in total

Review 1.  Genetic PrP Prion Diseases.

Authors:  Mee-Ohk Kim; Leonel T Takada; Katherine Wong; Sven A Forner; Michael D Geschwind
Journal:  Cold Spring Harb Perspect Biol       Date:  2018-05-01       Impact factor: 10.005

2.  Squirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathology.

Authors:  P Piccardo; J Cervenak; O Yakovleva; L Gregori; K Pomeroy; A Cook; F S Muhammad; T Seuberlich; L Cervenakova; D M Asher
Journal:  J Comp Pathol       Date:  2011-10-20       Impact factor: 1.311

3.  Clinical characterization of a kindred with a novel 12-octapeptide repeat insertion in the prion protein gene.

Authors:  Neeraj Kumar; Bradley F Boeve; Brendon P Boot; Carolyn F Orr; Joseph Duffy; Bryan K Woodruff; Anil K Nair; Jay Ellison; Karen Kuntz; Kejal Kantarci; Clifford R Jack; Barbara F Westmoreland; Julie A Fields; Matthew Baker; Rosa Rademakers; Joseph E Parisi; Dennis W Dickson
Journal:  Arch Neurol       Date:  2011-09

Review 4.  Hereditary Human Prion Diseases: an Update.

Authors:  Matthias Schmitz; Kathrin Dittmar; Franc Llorens; Ellen Gelpi; Isidre Ferrer; Walter J Schulz-Schaeffer; Inga Zerr
Journal:  Mol Neurobiol       Date:  2016-06-20       Impact factor: 5.590

5.  Conservation of a glycine-rich region in the prion protein is required for uptake of prion infectivity.

Authors:  Christopher F Harrison; Victoria A Lawson; Bradley M Coleman; Yong-Sun Kim; Colin L Masters; Roberto Cappai; Kevin J Barnham; Andrew F Hill
Journal:  J Biol Chem       Date:  2010-03-31       Impact factor: 5.157

6.  Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.

Authors:  P Piccardo; J J Liepnieks; A William; S R Dlouhy; M R Farlow; K Young; D Nochlin; T D Bird; R R Nixon; M J Ball; C DeCarli; O Bugiani; F Tagliavini; M D Benson; B Ghetti
Journal:  Am J Pathol       Date:  2001-06       Impact factor: 4.307

Review 7.  Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.

Authors:  Leonel T Takada; Mee-Ohk Kim; Ross W Cleveland; Katherine Wong; Sven A Forner; Ignacio Illán Gala; Jamie C Fong; Michael D Geschwind
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-01       Impact factor: 3.568

8.  Systematic investigation of predicted effect of nonsynonymous SNPs in human prion protein gene: a molecular modeling and molecular dynamics study.

Authors:  Samad Jahandideh; Degui Zhi
Journal:  J Biomol Struct Dyn       Date:  2013-03-25

9.  Signal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion protein.

Authors:  Neena S Rane; Oishee Chakrabarti; Lionel Feigenbaum; Ramanujan S Hegde
Journal:  J Cell Biol       Date:  2010-02-15       Impact factor: 10.539

10.  Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan.

Authors:  Nai-Fang Chi; Yi-Chung Lee; Yi-Chun Lu; Hsiu-Mei Wu; Bing-Wen Soong
Journal:  J Neurol       Date:  2009-08-21       Impact factor: 4.849

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