Journal Article

Nance–Horan syndrome protein, NHS, associates with epithelial cell junctions

Shiwani Sharma, Sharyn L. Ang, Marie Shaw, David A. Mackey, Jozef Gécz, John W. McAvoy and Jamie E. Craig

in Human Molecular Genetics

Volume 15, issue 12, pages 1972-1983
Published in print June 2006 | ISSN: 0964-6906
Published online May 2006 | e-ISSN: 1460-2083 | DOI: http://dx.doi.org/10.1093/hmg/ddl120
Nance–Horan syndrome protein, NHS, associates with epithelial cell junctions

Show Summary Details

Preview

Nance–Horan syndrome, characterized by congenital cataracts, craniofacial, dental abnormalities and mental disturbances, is an X-linked disorder with significant phenotypic heterogeneity. Affected individuals have mutations in the NHS (Nance–Horan syndrome) gene typically resulting in premature truncation of the protein. This report underlines the complexity of the regulation of the NHS gene that transcribes several isoforms. We demonstrate the differential expression of the two NHS isoforms, NHS-A and NHS-1A, and differences in the subcellular localization of the proteins encoded by these isoforms. This may in part explain the pleiotropic features of the syndrome. We show that the endogenous and exogenous NHS-A isoform localizes to the cell membrane of mammalian cells in a cell-type-dependent manner and that it co-localizes with the tight junction (TJ) protein ZO-1 in the apical aspect of cell membrane in epithelial cells. We also show that the NHS-1A isoform is a cytoplasmic protein. In the developing mammalian lens, we found continuous expression of NHS that became restricted to the lens epithelium in pre- and postnatal lens. Consistent with the in vitro findings, the NHS-A isoform associates with the apical cell membrane in the lens epithelium. This study suggests that disturbances in intercellular contacts underlie cataractogenesis in the Nance–Horan syndrome. NHS is the first gene localized at TJs that has been implicated in congenital cataracts.

Journal Article.  7612 words.  Illustrated.

Subjects: Genetics and Genomics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.