Kohrman Laboratory

The Kohrman Laboratory is interested in understanding the critical molecules required for development and function of the auditory and vestibular systems, the interactions between these molecules and the regulatory programs that control their expression. One of the lab's primary approaches is to identify genes that, when mutated, cause inherited inner ear disorders in the laboratory mouse. The mouse provides a well-characterized genetic system and a large collection of mutants that exhibit defects in hearing and balance. Identification of the defective genes in these mutants, along with analysis of their pathophysiology, will help researchers to understand gene function in the normal inner ear. Unraveling the genetic basis of inner ear disorders will also provide insight into the critical mechanisms that are required for development and function of this complex sense organ. Finally, these studies will accelerate the development of clinical interventions useful for treatment of hearing loss and vestibular dysfunction in humans.

Molecular analysis of mouse deafness mutants is providing access to critical components involved in a wide range of processes in the inner ear, including development, homeostasis, and neural signaling. Using a positional cloning strategy, the Kohrman Laboratory has identified the genes that underlie congenital deafness and vestibular dysfunction in two mouse mutants, 'pirouette' and 'spinner.' Based on evidence from pathology present in the mutants, these genes are required for the normal maturation of stereocilia, the specialized actin-filled structures on the surface of inner ear sensory cells that play a key role in mechanotransduction. The Kohrman Laboratory is using a variety of cell, molecular and genetic approaches to analyze the function of these genes, including expression of fluorescent hybrid proteins in explant cultures of the inner ear and the development of additional, transgenic mouse models. The lab is also investigating other mouse strains with hearing and balance defects, and collaborating with clinical geneticists to determine the role of the human versions of these mouse genes in hereditary hearing loss. The lab has helped to identify several mutations in the human spinner gene (TMIE) in individuals with early onset, profound hearing loss due to defects at the DFNB6 locus. As an initial step toward clinical therapies, the Kohrman Laboratory is currently developing gene therapy protocols to ameliorate hearing loss in our mouse model systems.