Genes Involved in the Development and Physiology of Both the Peripheral and Central Auditory Systems

被引:25
|
作者
Michalski, Nicolas [1 ,2 ,3 ]
Petit, Christine [1 ,2 ,3 ,4 ,5 ]
机构
[1] Inst Pasteur, Unite Genet & Physiol Audit, F-75015 Paris, France
[2] INSERM, UMRS 1120, F-75015 Paris, France
[3] Sorbonne Univ, F-75005 Paris, France
[4] Inst Vis, Syndrome Usher & Autres Atteintes Retino Cochleai, F-75012 Paris, France
[5] Coll France, F-75005 Paris, France
来源
基金
欧洲研究理事会;
关键词
hair cell; cochlea; auditory hindbrain; auditory cortex; evolution; gene regulatory networks; HAIR-CELL-DIFFERENTIATION; ANKLE-LINK COMPLEX; INNER-EAR; BRAIN-STEM; VESTIBULAR FUNCTION; SPIRAL GANGLION; RIBBON SYNAPSE; HEARING-LOSS; MOUSE MODEL; DEAFNESS;
D O I
10.1146/annurev-neuro-070918-050428
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The genetic approach, based on the study of inherited forms of deafness, has proven to be particularly effective for deciphering the molecular mechanisms underlying the development of the peripheral auditory system, the cochlea and its afferent auditory neurons, and how this system extracts the physical parameters of sound. Although this genetic dissection has provided little information about the central auditory system, scattered data suggest that some genes may have a critical role in both the peripheral and central auditory systems. Here, we review the genes controlling the development and function of the peripheral and central auditory systems, focusing on those with demonstrated intrinsic roles in both systems and highlighting the current underappreciation of these genes. Their encoded products are diverse, from transcription factors to ion channels, as are their roles in the central auditory system, mostly evaluated in brainstem nuclei. We examine the ontogenetic and evolutionary mechanisms that may underlie their expression at different sites.
引用
收藏
页码:67 / 86
页数:20
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