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Hum Mutat. 2015 Aug;36(8):753-7. doi: 10.1002/humu.22797. Epub 2015 Jun 22.

A Gain-of-Function Mutation in NALCN in a Child with Intellectual Disability, Ataxia, and Arthrogryposis.

Author information

1
Department of Biochemistry, Kyorin University School of Medicine, Tokyo, Japan.
2
CHU Sainte-Justine Research Center, Montreal, Canada.
3
Department of Neurosciences, University of Montreal, Montreal, Canada.
4
Department of Pediatrics, University of Montreal, Montreal, Canada.
5
Lunenfeld-Tanenbaum Research Institute and Institute of Medical Science, Department of Molecular Genetics, University of Toronto, Ontario, Canada.
6
Montreal Neurological Institute, McGill University, Montreal, Canada.

Abstract

NALCN and its homologues code for the ion channel responsible for half of background Na(+) -leak conductance in vertebrate and invertebrate neurons. Recessive mutations in human NALCN cause intellectual disability (ID) with hypotonia. Here, we report a de novo heterozygous mutation in NALCN affecting a conserved residue (p.R1181Q) in a girl with ID, episodic and persistent ataxia, and arthrogryposis. Interestingly, her episodes of ataxia were abolished by the administration of acetazolamide, similar to the response observed in episodic ataxia associated with other ion channels. Introducing the analogous mutation in the Caenorhabditis elegans homologue nca-1 induced a coiling locomotion phenotype, identical to that obtained with previously characterized C. elegans gain-of-function nca alleles, suggesting that p.R1181Q confers the same property to NALCN. This observation thus suggests that dominant mutations in NALCN can cause a neurodevelopmental phenotype that overlaps with, while being mostly distinct from that associated with recessive mutations in the same gene.

KEYWORDS:

C. elegans; NALCN; Na+-leak; de novo; gain-of-function

PMID:
25864427
DOI:
10.1002/humu.22797
[Indexed for MEDLINE]

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