Journal Article

Targeted disruption of mouse <i>Pds</i> provides insight about the inner-ear defects encountered in Pendred syndrome

Lorraine A. Everett, Inna A. Belyantseva, Konrad Noben-Trauth, Raquel Cantos, Amy Chen, Sneha I. Thakkar, Shelley L. Hoogstraten-Miller, Bechara Kachar, Doris K. Wu and Eric D. Green

in Human Molecular Genetics

Volume 10, issue 2, pages 153-161
Published in print January 2001 | ISSN: 0964-6906
Published online January 2001 | e-ISSN: 1460-2083 | DOI: http://dx.doi.org/10.1093/hmg/10.2.153
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

Show Summary Details

Preview

Following the positional cloning of PDS, the gene mutated in the deafness/goitre disorder Pendred syndrome (PS), numerous studies have focused on defining the role of PDS in deafness and PS as well as elucidating the function of the PDS-encoded protein (pendrin). To facilitate these efforts and to provide a system for more detailed study of the inner-ear defects that occur in the absence of pendrin, we have generated a Pds-knockout mouse. Pds–/– mice are completely deaf and also display signs of vestibular dysfunction. The inner ears of these mice appear to develop normally until embryonic day 15, after which time severe endolymphatic dilatation occurs, reminiscent of that seen radiologically in deaf individuals with PDS mutations. Additionally, in the second postnatal week, severe degeneration of sensory cells and malformation of otoconia and otoconial membranes occur, as revealed by scanning electron and fluorescence confocal microscopy. The ultrastructural defects seen in the Pds–/– mice provide important clues about the mechanisms responsible for the inner-ear pathology associated with PDS mutations.

Journal Article.  6907 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.