Neurodegeneration. C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits

Science. 2015 Jun 5;348(6239):1151-4. doi: 10.1126/science.aaa9344. Epub 2015 May 14.

Abstract

The major genetic cause of frontotemporal dementia and amyotrophic lateral sclerosis is a G4C2 repeat expansion in C9ORF72. Efforts to combat neurodegeneration associated with "c9FTD/ALS" are hindered by a lack of animal models recapitulating disease features. We developed a mouse model to mimic both neuropathological and clinical c9FTD/ALS phenotypes. We expressed (G4C2)66 throughout the murine central nervous system by means of somatic brain transgenesis mediated by adeno-associated virus. Brains of 6-month-old mice contained nuclear RNA foci, inclusions of poly(Gly-Pro), poly(Gly-Ala), and poly(Gly-Arg) dipeptide repeat proteins, as well as TDP-43 pathology. These mouse brains also exhibited cortical neuron and cerebellar Purkinje cell loss, astrogliosis, and decreased weight. (G4C2)66 mice also developed behavioral abnormalities similar to clinical symptoms of c9FTD/ALS patients, including hyperactivity, anxiety, antisocial behavior, and motor deficits.

Publication types

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

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Amyotrophic Lateral Sclerosis / pathology
  • Animals
  • Antisocial Personality Disorder / genetics
  • Antisocial Personality Disorder / pathology
  • C9orf72 Protein
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • DNA-Binding Proteins / genetics*
  • Dependovirus
  • Dipeptides / metabolism
  • Disease Models, Animal*
  • Frontotemporal Dementia / genetics*
  • Frontotemporal Dementia / pathology
  • Gene Transfer Techniques
  • HEK293 Cells
  • Humans
  • Mice*
  • Proteins / genetics*
  • Purkinje Cells / metabolism
  • Purkinje Cells / pathology
  • RNA, Nuclear / metabolism

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • DNA-Binding Proteins
  • Dipeptides
  • Proteins
  • RNA, Nuclear
  • glycylproline
  • N-glycylalanine