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RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiology.
Benkirane, Mehdi; Da Cunha, Dylan; Marelli, Cecilia; Larrieu, Lise; Renaud, Mathilde; Varilh, Jessica; Pointaux, Morgane; Baux, David; Ardouin, Olivier; Vangoethem, Charles; Taulan, Magali; Daumas Duport, Benjamin; Bergougnoux, Anne; Corbillé, Anne-Gaelle; Cossée, Mireille; Juntas Morales, Raul; Tuffery-Giraud, Sylvie; Koenig, Michel; Isidor, Bertrand; Vincent, Marie-Claire.
Afiliação
  • Benkirane M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Da Cunha D; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Marelli C; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Larrieu L; Department of Neurology, Montpellier Hospital, Montpellier, France.
  • Renaud M; Molecular Mechanisms of Neurodegenerative Dementia (MMDN), EPHE University of Montpellier, INSERM, Montpellier, France.
  • Varilh J; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Pointaux M; Department of Medical Genetics, Nancy Hospital, Nancy, France.
  • Baux D; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Ardouin O; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Vangoethem C; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Taulan M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Daumas Duport B; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Bergougnoux A; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Corbillé AG; Department of Radiology, Nantes Hospital, Nantes, France.
  • Cossée M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Juntas Morales R; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Tuffery-Giraud S; Department of Neurology, Nantes Hospital, Nantes, France.
  • Koenig M; Department of Molecular Genetics, Institut Universitaire de Recherche Clinique (IURC), Montpellier Hospital, Montpellier, France.
  • Isidor B; Genetics and Pathophysiology of NeuroMuscular Disorders, PhyMedExp Research Unit, CNRS, INSERM, University of Montpellier, Montpellier, France.
  • Vincent MC; Department of Neurology, Montpellier Hospital, Montpellier, France.
Brain ; 145(11): 3770-3775, 2022 11 21.
Article em En | MEDLINE | ID: mdl-35883251
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Doenças do Sistema Nervoso Periférico / Proteína de Replicação C / Vestibulopatia Bilateral Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Doenças do Sistema Nervoso Periférico / Proteína de Replicação C / Vestibulopatia Bilateral Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article