Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/53874
Type: Journal article
Title: Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
Author: Sharma, S.
Burdon, K.
Dave, A.
Jamieson, R.
Yaron, Y.
Billson, F.
van Maldergem, L.
Lorenz, B.
Gecz, J.
Craig, J.
Citation: Molecular Vision, 2008; 14(219-23):1856-1864
Publisher: Molecular Vision
Issue Date: 2008
ISSN: 1090-0535
1090-0535
Statement of
Responsibility: 
Shiwani Sharma, Kathryn P. Burdon, Alpana Dave, Robyn V. Jamieson, Yuval Yaron, Frank Billson, Lionel Van Maldergem, Birgit Lorenz, Jozef Gécz and Jamie E. Craig
Abstract: PURPOSE: Nance-Horan syndrome is typically characterized by severe bilateral congenital cataracts and dental abnormalities. Truncating mutations in the Nance-Horan syndrome (NHS) gene cause this X-linked genetic disorder. NHS encodes two isoforms, NHS-A and NHS-1A. The ocular lens expresses NHS-A, the epithelial and neuronal cell specific isoform. The NHS-A protein localizes in the lens epithelium at the cellular periphery. The data to date suggest a role for this isoform at cell-cell junctions in epithelial cells. This study aimed to identify the causative mutations in new patients diagnosed with Nance-Horan syndrome and to investigate the effect of mutations on subcellular localization of the NHS-A protein. METHODS: All coding exons of NHS were screened for mutations by polymerase chain reaction (PCR) and sequencing. PCR-based mutagenesis was performed to introduce three independent mutations in the NHS-A cDNA. Expression and localization of the mutant proteins was determined in mammalian epithelial cells. RESULTS: Truncating mutations were found in 6 out of 10 unrelated patients from four countries. Each of four patients carried a novel mutation (R248X, P264fs, K1198fs, and I1302fs), and each of the two other patients carried two previously reported mutations (R373X and R879X). No mutation was found in the gene in four patients. Two disease-causing mutations (R134fs and R901X) and an artificial mutation (T1357fs) resulted in premature truncation of the NHS-A protein. All three mutant proteins failed to localize to the cellular periphery in epithelial cells and instead were found in the cytoplasm. CONCLUSIONS: This study brings the total number of mutations identified in NHS to 18. The mislocalization of the mutant NHS-A protein, revealed by mutation analysis, is expected to adversely affect cell-cell junctions in epithelial cells such as the lens epithelium, which may explain cataractogenesis in Nance-Horan syndrome patients. Mutation analysis also shed light on the significance of NHS-A regions for its localization and, hence, its function at epithelial cell junctions.
Keywords: Cell Line; Animals; Dogs; Humans; Abnormalities, Multiple; Syndrome; Nuclear Proteins; Protein Isoforms; DNA Mutational Analysis; Mutagenesis; Base Sequence; Protein Transport; Mutation; Molecular Sequence Data; Male; Mutant Proteins
RMID: 0020083508
Published version: http://www.molvis.org/molvis/v14/a220/
Appears in Collections:Paediatrics publications

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