Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease

Neurobiol Aging. 2016 Jan:37:45-46. doi: 10.1016/j.neurobiolaging.2015.09.022. Epub 2015 Oct 9.

Abstract

A proportion of Alzheimer's disease cases displays inclusions of the RNA-binding protein, TDP-43. Considering the pathogenic role of tau mis-splicing, we compared tau isoform expression between Alzheimer's disease cases with or without TDP-43 inclusions. The average ratio of tau isoforms containing or lacking exon 10 (4R/3R ratio) or the total level of tau mRNA was not significantly different between cases with or without TDP-43 pathology in any of the brain regions examined. Although TDP-43 functions may be affected, TDP-43 does not critically regulate expression or splicing of tau in Alzheimer's disease suggesting that TDP-43 contributes to Alzheimer's disease through mechanisms independent of tau.

Keywords: Alzheimer's disease; Splicing; TDP-43; Tau; Tauopathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology
  • Brain / metabolism
  • Brain / pathology
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Exons
  • Gene Expression
  • Genetic Association Studies*
  • Humans
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Splicing / genetics*
  • RNA, Messenger / metabolism
  • tau Proteins / genetics*
  • tau Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • MAPT protein, human
  • Protein Isoforms
  • RNA, Messenger
  • TARDBP protein, human
  • tau Proteins