Transgenic and gene targeting studies of hair cell function in mouse inner ear

被引:21
作者
Zuo, J [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
来源
JOURNAL OF NEUROBIOLOGY | 2002年 / 53卷 / 02期
关键词
transgenesis; knock-out; Cre-loxP; CreER; promoter; bacterial artificial chromosome; hair cells; development; acetylcholine receptor; electromotility; mechanotransduction; adaptation; frequency tuning;
D O I
10.1002/neu.10128
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Despite the rapid discovery of a large number of genes in sensory hair cells of the inner ear, the functional roles of these genes in hair cells remain largely undetermined. Recent advances in transgenic and gene targeting technologies in mice have offered unprecedented opportunities to genetically manipulate the expression of these genes and to study their functional roles in hair cells in vivo. Transgenic analyses have revealed the presence of hair-cell-specific promoters in the genes encoding Math1, myosin VIIa, Pou4f3, and the 0 subunit of the acetylcholine receptor (alpha9 AChR). Targeted inactivation using embryonic stem cell technology and transgenic expression studies have revealed the roles of several genes involved in hair cell lineage (Math]), differentiation (Pou4f3), mechanotransduction (Myo1c, and Myo7a), electromotility (Prestin), and efferent modulation (Chrna9, encoding alpha9 AChR). Although many of these genes also play roles in other tissues, inactivation of these genes in hair cells alone will soon be possible by using the Cre-toxP system. Also imminent is the development of genetic methods to inactivate genes specifically in mouse hair cells at a desired time, by using inducible systems established in other types of neurons. Combining these types of manipulation of gene expression will enable hearing researchers to elucidate some of the fundamental and unique features of hair cell function such as mechanotransduction, frequency tuning, active mechanical amplification, and efferent modulation. (C) 2002 Wiley Periodicals, Inc. J Neurobiol 53: 286-305, 2002.
引用
收藏
页码:286 / 305
页数:20
相关论文
共 136 条
[1]   Genes expressed in neurons of adult male Drosophila [J].
Amrein, H ;
Axel, R .
CELL, 1997, 88 (04) :459-469
[2]  
[Anonymous], 1967, ACTA OTO-LARYNGOL
[3]   Functional identification of the mouse circadian Clock gene by transgenic BAC rescue [J].
Antoch, MP ;
Song, EJ ;
Chang, AM ;
Vitaterna, MH ;
Zhao, YL ;
Wilsbacher, LD ;
Sangoram, AM ;
King, DP ;
Pinto, LH ;
Takahashi, JS .
CELL, 1997, 89 (04) :655-667
[4]   A calcium responsive element that regulates expression of two calcium binding proteins in Purkinje cells [J].
Arnold, DB ;
Heintz, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (16) :8842-8847
[5]   Intracellular distributions and putative functions of calcium-binding proteins in the bullfrog vestibular otolith organs [J].
Baird, RA ;
Steyger, PS ;
Schuff, NR .
HEARING RESEARCH, 1997, 103 (1-2) :85-100
[6]  
BALSAMO G, 1969, J EMBRYOL EXP MORPH, V22, P327
[7]   Calcification processes in the chick otoconia and calcium binding proteins: patterns of tetracycline incorporation and calbindin-D28K distribution [J].
Balsamo, G ;
Avallone, B ;
Del Genio, F ;
Trapani, S ;
Marmo, FR .
HEARING RESEARCH, 2000, 148 (1-2) :1-8
[8]  
Beisel KW, 2000, MOL BRAIN RES, V82, P137
[9]  
Belyantseva IA, 2000, J NEUROSCI, V20, part. no.
[10]   Math1 is essential for genesis of cerebellar granule neurons [J].
BenArie, N ;
Bellen, HJ ;
Armstrong, DL ;
McCall, AE ;
Gordadze, PR ;
Guo, QX ;
Matzuk, MM ;
Zoghbi, HY .
NATURE, 1997, 390 (6656) :169-172