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RNA foci in two bi-allelic RFC1 expansion carriers.

Taishi WadaHiroshi DoiMasaki OkuboMikiko TadaNaohisa UedaHidefumi SuzukiWakana TominagaHaruki KoikeHiroyasu KomiyaShun KubotaShunta HashiguchiHaruko NakamuraKeita TakahashiMisako KuniiKenichi TanakaYosuke MiyajiYuichi HigashiyamaEriko KoshimizuSatoko MiyatakeMasahisa KatsunoSatoshi FujiiHidehisa TakahashiNaomichi MatsumotoHideyuki TakeuchiFumiaki Tanaka
Published in: Annals of neurology (2023)
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) is a late-onset, autosomal recessive neurodegenerative disorder caused by biallelic AAGGG/ACAGG repeat expansion (AAGGG-exp/ACAGG-exp) in RFC1. The recent identification of patients with CANVAS exhibiting compound heterozygosity for AAGGG-exp and truncating variants supports the loss-of-function of RFC1 in CANVAS patients. We investigated the pathological changes in two autopsied patients with CANVAS harboring biallelic ACAGG-exp and AAGGG-exp. RNA fluorescence in situ hybridization of the two patients revealed CCTGT- and CCCTT-containing RNA foci, respectively, in neuronal nuclei of tissues with neuronal loss. Our findings suggest that RNA toxicity may be involved in the pathogenesis of CANVAS. This article is protected by copyright. All rights reserved.
Keyphrases
  • late onset
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • early onset
  • prognostic factors
  • intellectual disability
  • oxidative stress
  • nucleic acid
  • copy number
  • subarachnoid hemorrhage