DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia

Ann Neurol. 2004 Jan;55(1):113-8. doi: 10.1002/ana.10782.

Abstract

Two novel mutations recently have been identified in the DJ-1 gene that cause a new form of autosomal recessive, early-onset parkinsonism. Because the pathological role of this protein is unknown, we examined the issue here and report the colocalization of DJ-1 protein within a subset of pathological tau inclusions in a diverse group of neurodegenerative disorders known as tauopathies. Our study extends the view that different neurodegenerative diseases may have similar pathological mechanisms, and that these processes likely include DJ-1.

Publication types

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

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Brain / metabolism
  • Brain / pathology*
  • COS Cells
  • Chlorocebus aethiops
  • Dementia / metabolism
  • Dementia / pathology*
  • HeLa Cells
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Inclusion Bodies / metabolism*
  • Inclusion Bodies / ultrastructure
  • Intracellular Signaling Peptides and Proteins
  • Middle Aged
  • Neurofibrillary Tangles / metabolism
  • Neurofibrillary Tangles / pathology
  • Oncogene Proteins / genetics
  • Oncogene Proteins / metabolism*
  • Parkinsonian Disorders / metabolism
  • Parkinsonian Disorders / pathology*
  • Protein Deglycase DJ-1
  • Transfection
  • tau Proteins / metabolism*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Oncogene Proteins
  • tau Proteins
  • PARK7 protein, human
  • Protein Deglycase DJ-1