RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiology

Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) is an inherited late-onset neurological disease caused by bi-allelic AAGGG pentanucleotide expansions within intron 2 of RFC1. Despite extensive studies, the pathophysiological mechanism of these intronic expansions remains elusive. We screened by clinical exome sequencing two unrelated patients presenting with late-onset ataxia. A repeat-primer polymerase chain reaction was used for RFC1 AAGGG intronic expansion identification. RFC1 mRNA expression was assessed by quantitative reverse transcription-polymerase chain reaction. We identified the first two CANVAS affected patients who are compound heterozygous for RFC1 truncating variants (p.Arg388* and c.575delA, respectively) and a pathological AAGGG expansion. RFC1 expression studies in whole blood showed a significant reduction of RFC1 mRNA for both patients compared to three patients with bi-allelic RFC1 expansions. In conclusion, this observation provides clues that suggest bi-allelic RFC1 conditional loss-of-function as the cause of the disease. Benkirane et al. identify two patients with CANVAS harbouring an RFC1 truncating variant and a pathological AAGGG expansion, thereby expanding the spectrum of CANVAS-associated mutations. RFC1 mRNA expression is reduced in both patients, providing clues to the underlying disease pathophysiology.

Automated summary

This study identifies two patients with CANVAS who have a truncating variant in RFC1 along with a pathological expansion. The reduced RFC1 mRNA expression in these patients provides clues to the underlying disease pathophysiology.