A native interactor scaffolds and stabilizes toxic ATAXIN-1 oligomers in SCA1

Elife. 2015 May 19;4:e07558. doi: 10.7554/eLife.07558.


Recent studies indicate that soluble oligomers drive pathogenesis in several neurodegenerative proteinopathies, including Alzheimer and Parkinson disease. Curiously, the same conformational antibody recognizes different disease-related oligomers, despite the variations in clinical presentation and brain regions affected, suggesting that the oligomer structure might be responsible for toxicity. We investigated whether polyglutamine-expanded ATAXIN-1, the protein that underlies spinocerebellar ataxia type 1, forms toxic oligomers and, if so, what underlies their toxicity. We found that mutant ATXN1 does form oligomers and that oligomer levels correlate with disease progression in the Atxn1(154Q/+) mice. Moreover, oligomeric toxicity, stabilization and seeding require interaction with Capicua, which is expressed at greater ratios with respect to ATXN1 in the cerebellum than in less vulnerable brain regions. Thus, specific interactors, not merely oligomeric structure, drive pathogenesis and contribute to regional vulnerability. Identifying interactors that stabilize toxic oligomeric complexes could answer longstanding questions about the pathogenesis of other proteinopathies.

Keywords: amyloid oligomers; ataxin-1; mouse; native interactors; neuroscience; proteinopathies.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Animals
  • Ataxin-1 / chemistry*
  • Ataxin-1 / toxicity*
  • Blotting, Western
  • Cerebellum / metabolism*
  • Chromatography, Gel
  • Enzyme-Linked Immunosorbent Assay
  • Immunohistochemistry
  • Immunoprecipitation
  • Mice
  • Peptides / analysis
  • Repressor Proteins / metabolism
  • Rotarod Performance Test
  • Spinocerebellar Ataxias / metabolism*
  • Spinocerebellar Ataxias / physiopathology*
  • Toxicity Tests


  • Ataxin-1
  • Atxn1 protein, mouse
  • Cic protein, mouse
  • Peptides
  • Repressor Proteins
  • polyglutamine