X-linked cataract and Nance-Horan syndrome are allelic disorders

• Published in: Human molecular genetics Vol. 18; no. 14; pp. 2643 - 2655
• Main Authors: Coccia, Margherita, Brooks, Simon P., Webb, Tom R., Christodoulou, Katja, Wozniak, Izabella O., Murday, Victoria, Balicki, Martha, Yee, Harris A., Wangensteen, Teresia, Riise, Ruth, Saggar, Anand K., Park, Soo-Mi, Kanuga, Naheed, Francis, Peter J., Maher, Eamonn R., Moore, Anthony T., Russell-Eggitt, Isabelle M., Hardcastle, Alison J.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 15.07.2009; Oxford Publishing Limited (England)
• Subjects: Adult; Base Sequence; Biological and medical sciences; Cataract - congenital; Cataract - genetics; Cataract - metabolism; Child; Child, Preschool; Female; Fundamental and applied biological sciences. Psychology; Gene Dosage; Genes, X-Linked; Genetic Diseases, X-Linked - genetics; Genetic Diseases, X-Linked - metabolism; Genetics of eukaryotes. Biological and molecular evolution; Humans; Infant, Newborn; Lens diseases; Male; Medical sciences; Middle Aged; Molecular and cellular biology; Molecular Sequence Data; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Ophthalmology; Pedigree; Young Adult; Sex linked character; Eye disease; Allele; Cataract; Lens disease; Genetics; X-Chromosome; Anterior segment disease; Syndrome
• ISSN: 0964-6906; 1460-2083; 1460-2083
• DOI: 10.1093/hmg/ddp206

Nance-Horan syndrome (NHS) is an X-linked developmental disorder characterized by congenital cataract, dental anomalies, facial dysmorphism and, in some cases, mental retardation. Protein truncation mutations in a novel gene (NHS) have been identified in patients with this syndrome. We previously mapped X-linked congenital cataract (CXN) in one family to an interval on chromosome Xp22.13 which encompasses the NHS locus; however, no mutations were identified in the NHS gene. In this study, we show that NHS and X-linked cataract are allelic diseases. Two CXN families, which were negative for mutations in the NHS gene, were further analysed using array comparative genomic hybridization. CXN was found to be caused by novel copy number variations: a complex duplication–triplication re-arrangement and an intragenic deletion, predicted to result in altered transcriptional regulation of the NHS gene. Furthermore, we also describe the clinical and molecular analysis of seven families diagnosed with NHS, identifying four novel protein truncation mutations and a novel large deletion encompassing the majority of the NHS gene, all leading to no functional protein. We therefore show that different mechanisms, aberrant transcription of the NHS gene or no functional NHS protein, lead to different diseases. Our data highlight the importance of copy number variation and non-recurrent re-arrangements leading to different severity of disease and describe the potential mechanisms involved.