Literature DB >> 30699050

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

Nicolas Michalski1,2,3, Christine Petit1,2,3,4,5.   

Abstract

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.

Entities:  

Keywords:  auditory cortex; auditory hindbrain; cochlea; evolution; gene regulatory networks; hair cell

Mesh:

Substances:

Year:  2019        PMID: 30699050     DOI: 10.1146/annurev-neuro-070918-050428

Source DB:  PubMed          Journal:  Annu Rev Neurosci        ISSN: 0147-006X            Impact factor:   12.449


  7 in total

1.  Impaired Hearing and Altered Subplate Circuits During the First and Second Postnatal Weeks of Otoferlin-Deficient Mice.

Authors:  Didhiti Mukherjee; Xiangying Meng; Joseph P Y Kao; Patrick O Kanold
Journal:  Cereb Cortex       Date:  2022-06-16       Impact factor: 4.861

Review 2.  Central auditory deficits associated with genetic forms of peripheral deafness.

Authors:  Nicolas Michalski; Christine Petit
Journal:  Hum Genet       Date:  2021-08-25       Impact factor: 5.881

3.  Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss.

Authors:  Limei Cui; Jing Zheng; Qiong Zhao; Jia-Rong Chen; Hanqing Liu; Guanghua Peng; Yue Wu; Chao Chen; Qiufen He; Haosong Shi; Shankai Yin; Rick A Friedman; Ye Chen; Min-Xin Guan
Journal:  JCI Insight       Date:  2020-12-03

4.  Overloaded Adeno-Associated Virus as a Novel Gene Therapeutic Tool for Otoferlin-Related Deafness.

Authors:  Vladan Rankovic; Christian Vogl; Nele M Dörje; Iman Bahader; Carlos J Duque-Afonso; Anupriya Thirumalai; Thomas Weber; Kathrin Kusch; Nicola Strenzke; Tobias Moser
Journal:  Front Mol Neurosci       Date:  2021-01-07       Impact factor: 5.639

Review 5.  The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.

Authors:  Sedigheh Delmaghani; Aziz El-Amraoui
Journal:  Hum Genet       Date:  2022-03-30       Impact factor: 5.881

6.  Unexpected Motherhood-Triggered Hearing Loss in the Two-Pore Channel (TPC) Mutant Mouse.

Authors:  Juliette Royer; José-Manuel Cancela; Jean-Marc Edeline
Journal:  Biomedicines       Date:  2022-07-15

7.  Expression pattern of cochlear microRNAs in the mammalian auditory hindbrain.

Authors:  Constanze Krohs; Mor Bordeynik-Cohen; Naama Messika-Gold; Ran Elkon; Karen B Avraham; Hans Gerd Nothwang
Journal:  Cell Tissue Res       Date:  2020-11-06       Impact factor: 5.249

  7 in total

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