10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

      Proceedings of the National Academy of Sciences of the United States of America
      Adult, Alleles, Amino Acid Sequence, Amyloid beta-Protein Precursor, genetics, Animals, Base Sequence, Brain, pathology, Cloning, Molecular, methods, Creutzfeldt-Jakob Syndrome, physiopathology, transmission, Crossing Over, Genetic, Female, Humans, Male, Middle Aged, Molecular Sequence Data, Mutation, Oligodeoxyribonucleotides, Phenotype, Polymerase Chain Reaction, PrPSc Proteins, Primates, Prions, Repetitive Sequences, Nucleic Acid

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The PRNP gene, encoding the amyloid precursor protein that is centrally involved in Creutzfeldt-Jakob disease (CJD), has an unstable region of five variant tandem octapeptide coding repeats between codons 51 and 91. We screened a total of 535 individuals for the presence of extra repeats in this region, including patients with sporadic and familial forms of spongiform encephalopathy, members of their families, other neurological and non-neurological patients, and normal controls. We identified three CJD families (in each of which the proband's disease was neuropathologically confirmed and experimentally transmitted to primates) that were heterozygous for alleles with 10, 12, or 13 repeats, some of which had "wobble" nucleotide substitutions. We also found one individual with 9 repeats and no nucleotide substitutions who had no evidence of neurological disease. These observations, together with data on published British patients with 11 and 14 repeats, strongly suggest that the occurrence of 10 or more octapeptide repeats in the encoded amyloid precursor protein predisposes to CJD.

          Related collections

          Author and article information

          Comments

          Comment on this article