Electromotility is a unique characteristic of the outer hair cells (OHC) of the mammalian cochlea. This electromotility is thought to underlie the exquisite frequency selectivity and sensitivity of mammalian hearing. Recently, we cloned the gene for the protein prestin, and have determined that prestin is the key molecule responsible for OHC electromotility. However, other proteins have been shown to modify prestin's activity, thereby affecting hearing function. Currently, the precise identities of these prestin-associated proteins (PAPs) are unknown, and the interactions between prestin and PAPs have not been described at the molecular level. Thus, the overall aim of our proposed research is to identify PAPs and to characterize their function. First, we propose to identify PAPs using a newly developed membrane-based yeast two-hybrid selective method (Aim I). An OHC-cDNA library suitable for that method will be built to increase the sensitivity and to decrease the false positive clones of library screening. Then, using prestin as """"""""bait,"""""""" we will use the yeast two-hybrid method to identify PAPs. Because of its highly sensitive nature, the yeast two-hybrid method is able to identify PAPs that can not be recognized by other methods. Second, we propose to identify PAPs using a second method: combined mass spectrometry analysis with prestin coimmunoprecipitation (Aim II). The major advantage of this method is its ability to identify physiologically relevant Prestin-PAP interactions that exist in vivo. Finally, after PAPs have been identified using either the two complementary methods or from other sources, we will determine whether those PAPs reside in OHCs in vivo, and will characterize the mechanisms by which PAPs modify prestin's function (Aim III). Taken together, these experiments will further our understanding of the molecular basis of OHC-based cochlear amplification, and potentially lead to identification of PAP-related deafness genes. This knowledge may make it possible to manipulate OHC function for therapeutic purposes.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC006412-02
Application #
7020704
Study Section
Special Emphasis Panel (ZRG1-IFCN-A (93))
Program Officer
Watson, Bracie
Project Start
2005-04-01
Project End
2008-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
2
Fiscal Year
2006
Total Cost
$289,395
Indirect Cost
Name
Northwestern University at Chicago
Department
Other Health Professions
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Zheng, Jing; Miller, Katharine K; Yang, Tao et al. (2011) Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4). Proc Natl Acad Sci U S A 108:4218-23
Sengupta, Soma; Miller, Katharine K; Homma, Kazuaki et al. (2010) Interaction between the motor protein prestin and the transporter protein VAPA. Biochim Biophys Acta 1803:796-804
Zheng, Lili; Zheng, Jing; Whitlon, Donna S et al. (2010) Targeting of the hair cell proteins cadherin 23, harmonin, myosin XVa, espin, and prestin in an epithelial cell model. J Neurosci 30:7187-201
Homma, Kazuaki; Miller, Katharine K; Anderson, Charles T et al. (2010) Interaction between CFTR and prestin (SLC26A5). Biochim Biophys Acta 1798:1029-40
Zheng, Jing; Anderson, Charles T; Miller, Katharine K et al. (2009) Identifying components of the hair-cell interactome involved in cochlear amplification. BMC Genomics 10:127
Sengupta, Soma; George, Manju; Miller, Katharine K et al. (2009) EHD4 and CDH23 are interacting partners in cochlear hair cells. J Biol Chem 284:20121-9
Dallos, Peter; Wu, Xudong; Cheatham, Mary Ann et al. (2008) Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron 58:333-9
Wu, Xudong; Wang, Xiang; Gao, Jiangang et al. (2008) Glucose transporter 5 is undetectable in outer hair cells and does not contribute to cochlear amplification. Brain Res 1210:20-8
Anderson, Charles T; Zheng, Jing (2007) Isolation of outer hair cells from the cochlear sensory epithelium in whole-mount preparation using laser capture microdissection. J Neurosci Methods 162:229-36
Zheng, Jing; Du, Guo-Guang; Anderson, Charles T et al. (2006) Analysis of the oligomeric structure of the motor protein prestin. J Biol Chem 281:19916-24

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