TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Science. 2008 Mar 21;319(5870):1668-72. doi: 10.1126/science.1154584. Epub 2008 Feb 28.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder characterized pathologically by ubiquitinated TAR DNA binding protein (TDP-43) inclusions. The function of TDP-43 in the nervous system is uncertain, and a mechanistic role in neurodegeneration remains speculative. We identified neighboring mutations in a highly conserved region of TARDBP in sporadic and familial ALS cases. TARDBPM337V segregated with disease within one kindred and a genome-wide scan confirmed that linkage was restricted to chromosome 1p36, which contains the TARDBP locus. Mutant forms of TDP-43 fragmented in vitro more readily than wild type and, in vivo, caused neural apoptosis and developmental delay in the chick embryo. Our evidence suggests a pathophysiological link between TDP-43 and ALS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Amino Acid Substitution
  • Amyotrophic Lateral Sclerosis / genetics*
  • Animals
  • Apoptosis
  • CHO Cells
  • Chick Embryo
  • Chromosomes, Human, Pair 1 / genetics
  • Cricetinae
  • Cricetulus
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / physiology
  • Embryonic Development
  • Female
  • Humans
  • Male
  • Microsatellite Repeats
  • Middle Aged
  • Molecular Sequence Data
  • Mutant Proteins / chemistry
  • Mutant Proteins / physiology
  • Mutation, Missense*
  • Neurons / cytology
  • Neurons / physiology

Substances

  • DNA-Binding Proteins
  • Mutant Proteins