Usher syndrome (USH) is an autosomal recessive disorder characterized by progressive retinitis pigmentosa (RP) and moderate to profound sensorineural hearing loss. USH is the leading cause of combined deafness and blindness in the world and about 50% of all cases of combined deafness and blindness in the United States are due to Usher syndrome. The three major clinical subtypes (USH type I, USH type II and USH type III) are distinguished by severity of hearing loss and by the presence or absence of vestibular dysfunction. USH type I is genetically heterogeneous and the phenotype is the most severe of the three types of USH. Seven genetic loci have been mapped for USH1 and genes for five of them have been identified. At least three more genes for USH type I remain to be identified. In collaborations with scientists around the world, Dr. Friedman's lab has an unprecedented genetic resource to identify and study the genes involved in nonsyndromic as well as syndromic hearing impairment. From this resource, 1 have developed a unique collection of USH type I families with no mutations in the known USH genes and are either linked to USH1H locus or unlinked to known USH1 loci. As the Principal Investigator, my goal is to use these USH type I families forthe mapping and identification of new USH1 genes, including USH1H. My publication record on USH is indicative of my abilities to successfully conduct this research. My career goals are to understand the genetic and molecular basis of hearing processes through the identification and functional dissection of the genes involved in deafness. There are three specific aims of this proposal: 1) enrollment of additional families with an USHI phenotype and mutational screening of known USH loci, 2) linkage analyses to map the loci for USH1, and 3) positionally cloning of USHI H and additional USHI genes. Identification and characterization of these genes will enhance diagnostic accuracy and improve genetic counseling. Molecular dissection of USH will reveal important new information about the developmental, metabolic and/or regulatory pathways common to norma! retinal and auditory function.

Public Health Relevance

The knowledge gained from this study will improve our understanding of the biology and pathophysiology of the hearing and visual systems. A better understanding of the underlying causes of USH is a critical first step towards the development of effective therapies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Transition Award (R00)
Project #
5R00DC009287-04
Application #
8117800
Study Section
Special Emphasis Panel (NSS)
Program Officer
Sklare, Dan
Project Start
2007-11-14
Project End
2012-07-31
Budget Start
2011-08-01
Budget End
2012-07-31
Support Year
4
Fiscal Year
2011
Total Cost
$236,105
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
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Jaworek, Thomas J; Bhatti, Rashid; Latief, Noreen et al. (2012) USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1. J Hum Genet 57:633-7
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