Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

Neurosci Lett. 2001 Oct 5;311(3):145-8. doi: 10.1016/s0304-3940(01)02109-7.


The microtubule associated protein, tau, is found in fibrillar lesions that characterise progressive supranuclear palsy (PSP) and related tauopathies. Mutations in the tau gene in frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) and genetic association of the H1 haplotype of the tau gene with PSP has firmly established a direct role for tau in disease pathogenesis. However, the functional significance of the tau genetic association in PSP is unknown. We analysed the tau gene promoter sequence and identified two novel single nucleotide polymorphisms. Here we report the genetic association of a novel tau promoter haplotype with PSP which may influence tau transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mutational Analysis
  • Gene Frequency / physiology
  • Haplotypes / genetics*
  • Humans
  • Linkage Disequilibrium / physiology
  • Polymorphism, Single Nucleotide / physiology*
  • Promoter Regions, Genetic / physiology*
  • Proto-Oncogene Proteins c-myb / genetics
  • Supranuclear Palsy, Progressive / genetics*
  • tau Proteins / genetics*


  • Proto-Oncogene Proteins c-myb
  • tau Proteins