An antisense CAG repeat transcript at JPH3 locus mediates expanded polyglutamine protein toxicity in Huntington's disease-like 2 mice

Neuron. 2011 May 12;70(3):427-40. doi: 10.1016/j.neuron.2011.03.021.

Abstract

Huntington's disease-like-2 (HDL2) is a phenocopy of Huntington's disease caused by CTG/CAG repeat expansion at the Junctophilin-3 (JPH3) locus. The mechanisms underlying HDL2 pathogenesis remain unclear. Here we developed a BAC transgenic mouse model of HDL2 (BAC-HDL2) that exhibits progressive motor deficits, selective neurodegenerative pathology, and ubiquitin-positive nuclear inclusions (NIs). Molecular analyses reveal a promoter at the transgene locus driving the expression of a CAG repeat transcript (HDL2-CAG) from the strand antisense to JPH3, which encodes an expanded polyglutamine (polyQ) protein. Importantly, BAC-HDL2 mice, but not control BAC mice, accumulate polyQ-containing NIs in a pattern strikingly similar to those in the patients. Furthermore, BAC mice with genetic silencing of the expanded CUG transcript still express HDL2-CAG transcript and manifest polyQ pathogenesis. Finally, studies of HDL2 mice and patients revealed CBP sequestration into NIs and evidence for interference of CBP-mediated transcriptional activation. These results suggest overlapping polyQ-mediated pathogenic mechanisms in HD and HDL2.

Publication types

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

MeSH terms

  • Age Factors
  • Analysis of Variance
  • Animals
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Chromatin Immunoprecipitation / methods
  • Disease Models, Animal
  • Embryo, Mammalian
  • Gene Expression Regulation / genetics
  • Humans
  • Huntington Disease* / drug therapy
  • Huntington Disease* / genetics
  • Huntington Disease* / physiopathology
  • Intranuclear Inclusion Bodies / metabolism
  • Intranuclear Inclusion Bodies / pathology
  • Membrane Proteins / genetics*
  • Mice
  • Mice, Transgenic
  • Motor Activity / genetics
  • Neurons / metabolism
  • Oligodeoxyribonucleotides, Antisense / metabolism*
  • Organ Size / genetics
  • Peptides / genetics
  • Peptides / toxicity*
  • Time Factors
  • Transfection
  • Trinucleotide Repeat Expansion / genetics*
  • Ubiquitin / metabolism

Substances

  • Membrane Proteins
  • Oligodeoxyribonucleotides, Antisense
  • Peptides
  • Ubiquitin
  • junctophilin
  • polyglutamine