An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype

Ann Neurol. 2002 Oct;52(4):511-6. doi: 10.1002/ana.10340.


MAPT, the gene encoding tau, was screened for mutations in 96 progressive supranuclear palsy subjects. A point mutation (R5L) was identified in a single progressive supranuclear palsy subject that was not in the other progressive supranuclear palsy subjects or in 96 controls. Functionally, this mutation alters the ability of tau to promote microtubule assembly. Analysis of soluble tau from different brain regions indicates that the mutation does not affect the ratio of tau isoforms synthesized. Aggregated insoluble tau from subcortical regions was predominantly four-repeat tau with no or one amino terminal insert (0N4R and 1N4R). Insoluble tau from cortical regions also contained 1N3R tau. Thus, the R5L mutation causes a progressive supranuclear palsy phenotype, presumably by a gain-of-function mechanism.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Exons / genetics
  • Female
  • Humans
  • Middle Aged
  • Molecular Sequence Data
  • Phenotype
  • Supranuclear Palsy, Progressive / genetics*
  • Tauopathies / genetics*
  • Tauopathies / pathology
  • tau Proteins / genetics*


  • tau Proteins