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http://purl.uniprot.org/citations/22693284http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22693284http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22693284http://www.w3.org/2000/01/rdf-schema#comment"

Background

Non-progressive congenital ataxias (NPCA) with or without intellectual disability (ID) are clinically and genetically heterogeneous conditions. As a consequence, the identification of the genes responsible for these phenotypes remained limited.

Objective

Identification of a new gene responsible for NPCA and ID. Methods Following the discovery of three familial or sporadic cases with an intragenic calmodulin-binding transcription activator 1 (CAMTA1) rearrangement identified by an array-CGH and recruited from a national collaboration, the authors defined the clinical and molecular characteristics of such rearrangements, and searched for patients with point mutations by direct sequencing.

Results

Intragenic copy number variations of CAMTA1 were all located in the CG-1 domain of the gene. It segregated with autosomal dominant ID with non-progressive congenital cerebellar ataxia (NPCA) in two unrelated families, and was de novo deletion located in the same domain in a child presenting with NPCA. In the patients with ID, the deletion led to a frameshift, producing a truncated protein, while this was not the case for the patient with isolated childhood ataxia. Brain MRI of the patients revealed a pattern of progressive atrophy of cerebellum medium lobes and superior vermis, parietal lobes and hippocampi. DNA sequencing of the CG-1 domain in 197 patients with sporadic or familial non-syndromic intellectual deficiency, extended to full DNA sequencing in 50 patients with ID and 47 additional patients with childhood ataxia, identified no pathogenic mutation.

Conclusion

The authors have evidence that loss-of-function of CAMTA1, a brain-specific calcium responsive transcription factor, is responsible for NPCA with or without ID. Accession numbers CAMTA1 reference sequence used was ENST00000303635. Protein sequence was ENSP00000306522."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.org/dc/terms/identifier"doi:10.1136/jmedgenet-2012-100856"xsd:string
http://purl.uniprot.org/citations/22693284http://purl.org/dc/terms/identifier"doi:10.1136/jmedgenet-2012-100856"xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Heron D."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Heron D."xsd:string
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http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Bonnet C."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Bonnet C."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Brice A."xsd:string
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http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Lopez E."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Lopez E."xsd:string
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http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Amiel J."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Amiel J."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Charles P."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Charles P."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Depienne C."xsd:string
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http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Mignot C."xsd:string
http://purl.uniprot.org/citations/22693284http://purl.uniprot.org/core/author"Mignot C."xsd:string
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