A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy

Exp Neurol. 2003 Nov;184(1):131-40. doi: 10.1016/s0014-4886(03)00393-5.

Abstract

A novel mutation in exon 9 of tau, I260V, is associated with a clinical syndrome consistent with frontotemporal dementia with extensive tau pathology; however, neurofibrillary tangles and Pick bodies are absent. Significantly, Sarkosyl-insoluble tau extracted from affected brain tissue consisted almost exclusively of four-repeat isoforms. Consistent with these findings, in vitro biochemical assays demonstrated that the I260V mutation causes a selective increase in tau aggregation and a decrease in tau-induced microtubule assembly with four-repeat isoforms only. The contrasting pathology and biochemical effects of this mutation suggest a different disease mechanism from the other exon 9 mutations and demonstrates the critical role for the first microtubule-binding domain in tau-promoted microtubule assembly and the pathogenic aggregation of tau.

Publication types

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

MeSH terms

  • Aged
  • Amino Acid Sequence
  • DNA / genetics
  • Dementia / genetics*
  • Dementia / pathology*
  • Exons / genetics
  • Frontal Lobe / pathology*
  • Heparin / pharmacology
  • Humans
  • Immunohistochemistry
  • Microtubules / ultrastructure
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed / genetics
  • Mutation / genetics*
  • Phenotype
  • Reverse Transcriptase Polymerase Chain Reaction
  • Temporal Lobe / pathology*
  • tau Proteins / genetics*

Substances

  • tau Proteins
  • Heparin
  • DNA