A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease

Ann Neurol. 2002 Mar;51(3):373-6. doi: 10.1002/ana.10140.

Abstract

Mutations in the tau gene cause familial frontotemporal dementia and parkinsonism linked to chromosome 17. In this article, we describe a novel missense mutation, S320F, in the tau gene in a family with presenile dementia. To our knowledge, it is the first mutation to be described in exon 11 of tau. The proband died at age 53 years, after a disease duration of 15 years, and autopsy revealed a neuropathological picture similar to Pick's disease. Recombinant tau protein with the S320F mutation showed a greatly reduced ability to promote microtubule assembly.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology*
  • DNA / genetics
  • Exons / genetics
  • Humans
  • Inclusion Bodies / diagnostic imaging*
  • Male
  • Microscopy, Electron
  • Microtubules / drug effects
  • Microtubules / physiology
  • Mutation, Missense / physiology*
  • Pick Disease of the Brain / pathology*
  • Recombinant Proteins / pharmacology
  • Ultrasonography
  • tau Proteins / genetics*
  • tau Proteins / pharmacology

Substances

  • Recombinant Proteins
  • tau Proteins
  • DNA