Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17

Science. 1998 Dec 4;282(5395):1914-7. doi: 10.1126/science.282.5395.1914.

Abstract

Tau proteins aggregate as cytoplasmic inclusions in a number of neurodegenerative diseases, including Alzheimer's disease and hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Over 10 exonic and intronic mutations in the tau gene have been identified in about 20 FTDP-17 families. Analyses of soluble and insoluble tau proteins from brains of FTDP-17 patients indicated that different pathogenic mutations differentially altered distinct biochemical properties and stoichiometry of brain tau isoforms. Functional assays of recombinant tau proteins with different FTDP-17 missense mutations implicated all but one of these mutations in disease pathogenesis by reducing the ability of tau to bind microtubules and promote microtubule assembly.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alternative Splicing
  • Brain / metabolism*
  • Cerebellum / metabolism
  • Chromosomes, Human, Pair 17
  • Dementia / genetics*
  • Dementia / metabolism
  • Frontal Lobe / metabolism
  • Humans
  • Microtubules / metabolism*
  • Mutation
  • Mutation, Missense
  • Parkinson Disease, Secondary / genetics*
  • Parkinson Disease, Secondary / metabolism
  • Phosphorylation
  • Protein Isoforms / chemistry
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Recombinant Proteins / metabolism
  • Solubility
  • Syndrome
  • tau Proteins / chemistry
  • tau Proteins / genetics*
  • tau Proteins / metabolism*

Substances

  • Protein Isoforms
  • Recombinant Proteins
  • tau Proteins