Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations

Hum Mol Genet. 2015 Jun 15;24(12):3529-44. doi: 10.1093/hmg/ddv104. Epub 2015 Mar 19.

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the loss of motor neuron-like cells. Mutations in the RNA- and DNA-binding proteins, fused in sarcoma (FUS) and transactive response DNA-binding protein 43 kDa (TDP-43), are responsible for 5-10% of familial and 1% of sporadic ALS cases. Importantly, aggregation of misfolded FUS or TDP-43 is also characteristic of several neurodegenerative disorders in addition to ALS, including frontotemporal lobar degeneration. Moreover, splicing deregulation of FUS and TDP-43 target genes as well as mitochondrial abnormalities are associated with disease-causing FUS and TDP-43 mutants. While progress has been made to understand the functions of these proteins, the exact mechanisms by which FUS and TDP-43 cause ALS remain unknown. Recently, we discovered that, in addition to being up-regulated in spinal cords of ALS patients, the novel protein oxidative resistance 1 (Oxr1) protects neurons from oxidative stress-induced apoptosis. To further understand the function of Oxr1, we present here the first interaction study of the protein. We show that Oxr1 binds to Fus and Tdp-43 and that certain ALS-associated mutations in Fus and Tdp-43 affect their Oxr1-binding properties. We further demonstrate that increasing Oxr1 levels in cells expressing specific Fus and Tdp-43 mutants improves the three main cellular features associated with ALS: cytoplasmic mis-localization and aggregation, splicing changes of a mitochondrial gene and mitochondrial defects. Taken together, these findings suggest that OXR1 may have therapeutic benefits for the treatment of ALS and related neurodegenerative disorders with TDP-43 pathology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Amyotrophic Lateral Sclerosis / metabolism*
  • Animals
  • Arginine / metabolism
  • Autophagy / genetics
  • Cytoplasm / metabolism
  • DNA-Binding Proteins / genetics*
  • Humans
  • Methylation
  • Mice
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mutation*
  • Oxidative Stress
  • Proteasome Endopeptidase Complex / metabolism
  • Protein Aggregation, Pathological
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Isoforms
  • Proteins / chemistry
  • Proteins / genetics*
  • Proteins / metabolism*
  • Proteolysis
  • RNA Splicing
  • RNA-Binding Protein FUS / genetics*
  • Transcription, Genetic

Substances

  • DNA-Binding Proteins
  • Mitochondrial Proteins
  • OXR1 protein, human
  • Protein Isoforms
  • Proteins
  • RNA-Binding Protein FUS
  • Arginine
  • Proteasome Endopeptidase Complex