Volume 11 Issue 217
Published - 14:00 UTC 08:00 EST 21-Aug-2009 
Next Update - 14:00 UC 08:00 EST 22-Aug-2009

Editor: Susan K. Boyer, RN
Vidyya.
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Gene discovery reveals a critical protein's function in hearing

(21 August 2009: VIDYYA MEDICAL NEWS SERVICE) -- Discovery of a deafness-causing gene defect in mice has helped identify a new protein that protects sensory cells in the ear, according to a study led by University of Iowa researchers. The findings, which also involved Kansas State University, appear in the Aug. 21 issue of the open-access journal PLoS Genetics.

In humans, hereditary deafness is one of the most common birth defects, yet most genes involved in hearing are unidentified. Mice are used as research models because mouse and human auditory genetics are very similar.

Using a deaf mouse model generated at The Jackson Laboratory, the team identified the deafness-causing defect in the claudin-9 gene. The mutated gene fails to produce normal claudin-9 protein, which, the University of Iowa team showed, is needed to maintain the proper distribution of potassium in the inner ear.

"Genes in the claudin family number at least 24 and produce proteins that prevent ions, including potassium, from moving between cells," said the paper's senior author Botond Banfi, M.D., Ph.D., assistant professor of anatomy and cell biology in the University of Iowa Carver College of Medicine. "Sensory cells in the hearing organ are bathed in a high potassium solution on one side and in a low potassium solution on the other side. We found that claudin-9 is very important in keeping the amount of potassium on the two sides separate. This separation protects sensory cells from potassium intoxication."

When claudin-9 is mutated, potassium floods the wrong part of the sensory cells, killing most and leaving the remaining ones functionally defective.

In follow-up efforts, Banfi and colleagues, including the study's first author Yoko Nakano, Ph.D., University of Iowa assistant research scientist in anatomy and cell biology, are screening people with hearing impairment to see if some of them have a mutation in claudin-9.

http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000610

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