A large number of genes have recently been identified that are implicated in vestibular disorders and in development of inner ear hair cells. Mouse models in which these genes can be inactivated in a hair cell-specific, temporally controlled manner are crucial to in vivo functional studies of these genes. However, to date there has been no effective method of conditional gene targeting in hair cells in vivo. This proposal seeks to overcome the limitations of traditional transgenic methods by expressing the bacterial recombinase Cre specifically and inducibly in vestibular and cochlear hair cells in transgenic mice. Preliminary studies have succeeded in creating and characterizing transgenic mice in which the reporter gene green fluorescent protein (GFP) is expressed specifically and abundantly in developing and adult hair cells of the vestibular and cochlear sensory epithelia. This success was achieved through the novel approach of modifying a bacterial artificial chromosome (BAC) that contains the alpha-9 AChR gene, which is important to efferent innervation and specific to vestibular and cochlear hair cells.
The specific aims of this proposal are to: 1. Create mice in which Cre is expressed specifically in vestibular and cochlear hair cells. 2. Create mice in which Cre is activated specifically in vestibular and cochlear hair cells only when an exogenous ligand is delivered. The creation and characterization of these Cre-hair cell mice will greatly facilitate studies of gene function in sensory-motor systems responsive to gravity. Ultimately, such studies will also contribute to the understanding, prevention, and treatment of vestibular diseases in humans. All mice made in FVB/N strain will be available to the academic community.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21DC005168-02
Application #
6523514
Study Section
Special Emphasis Panel (ZDC1-SRB-O (21))
Program Officer
Platt, Christopher
Project Start
2001-08-01
Project End
2004-07-30
Budget Start
2002-08-01
Budget End
2003-07-31
Support Year
2
Fiscal Year
2002
Total Cost
$150,000
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Liu, Zhiyong; Owen, Thomas; Fang, Jie et al. (2012) Overactivation of Notch1 signaling induces ectopic hair cells in the mouse inner ear in an age-dependent manner. PLoS One 7:e34123
Kurt, Simone; Sausbier, Matthias; Ruttiger, Lukas et al. (2012) Critical role for cochlear hair cell BK channels for coding the temporal structure and dynamic range of auditory information for central auditory processing. FASEB J 26:3834-43
Liu, Zhiyong; Walters, Brandon J; Owen, Thomas et al. (2012) Regulation of p27Kip1 by Sox2 maintains quiescence of inner pillar cells in the murine auditory sensory epithelium. J Neurosci 32:10530-40
Liu, Zhiyong; Owen, Thomas; Fang, Jie et al. (2012) In vivo Notch reactivation in differentiating cochlear hair cells induces Sox2 and Prox1 expression but does not disrupt hair cell maturation. Dev Dyn 241:684-96
Liu, Zhiyong; Dearman, Jennifer A; Cox, Brandon C et al. (2012) Age-dependent in vivo conversion of mouse cochlear pillar and Deiters' cells to immature hair cells by Atoh1 ectopic expression. J Neurosci 32:6600-10
Caddy, Jacinta; Wilanowski, Tomasz; Darido, Charbel et al. (2010) Epidermal wound repair is regulated by the planar cell polarity signaling pathway. Dev Cell 19:138-47
Liu, Zhiyong; Owen, Thomas; Zhang, Lingli et al. (2010) Dynamic expression pattern of Sonic hedgehog in developing cochlear spiral ganglion neurons. Dev Dyn 239:1674-83
Winter, Harald; Rüttiger, Lukas; Müller, Marcus et al. (2009) Deafness in TRbeta mutants is caused by malformation of the tectorial membrane. J Neurosci 29:2581-7
Yu, Yiling; Zuo, Jian (2009) The practical use of Cre and loxP technologies in mouse auditory research. Methods Mol Biol 493:87-102
Weber, Thomas; Corbett, Mary K; Chow, Lionel M L et al. (2008) Rapid cell-cycle reentry and cell death after acute inactivation of the retinoblastoma gene product in postnatal cochlear hair cells. Proc Natl Acad Sci U S A 105:781-5

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