CASZ1 regulates the maturation of outer hair cells and is required for hearing in mice

The transcription factor ATOH1 is a master regulator of mechanosensory hair-cell (HC) development in the ear. Here, we report that its target gene Casz1 regulates the maturation of outer HCs (OHCs). Genetic deletion of Casz1 during (but not after) cochlear development in the mouse caused: hearing loss; disorganization of mechanosensory stereocilia bundles in OHCs; reduced F-actin density in OHC cuticular plates; progressive OHC loss; and mild morphological alterations in inner HCs. This deletion also altered gene expression, delaying downregulation of genes expressed in immature OHCs, including the actin regulator-encoding gene Coro2a , and accelerating upregulation of genes expressed in mature OHCs. Deleting Coro2a in Casz1 mutant mice restored F-actin density in cuticular plates but increased stereocilia bundle disorganization and hearing thresholds, revealing that CORO2A provides an overall beneficial effect. Our data indicate that CASZ1 regulates transcriptional and morphological maturation of OHCs, and that CASZ1 in maturing HCs is necessary for hearing.

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Publication Details

Journal
iScience
Published
2026-08-27
DOI
https://doi.org/10.1016/j.isci.2026.117341
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00

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article

CASZ1 regulates the maturation of outer hair cells and is required for hearing in mice

Robert J. Morell, Chantal Allamargot, Susan Wiechert, Braulio Peguero et al.
iScience
Hearing, Cochlea, Tinnitus, Genetics
article

CASZ1 regulates the maturation of outer hair cells and is required for hearing in mice

Robert J. Morell, Chantal Allamargot, Susan Wiechert, Braulio Peguero, Botond Bánfi, Angelika Doetzlhofer, Yoko Nakano, Matthew W. Kelley, Rebecca Hipp, Ning Hu, Erich T. Boger, Elizabeth C. Driver, Steven H. Green
article en

Abstract

The transcription factor ATOH1 is a master regulator of mechanosensory hair-cell (HC) development in the ear. Here, we report that its target gene Casz1 regulates the maturation of outer HCs (OHCs). Genetic deletion of Casz1 during (but not after) cochlear development in the mouse caused: hearing loss; disorganization of mechanosensory stereocilia bundles in OHCs; reduced F-actin density in OHC cuticular plates; progressive OHC loss; and mild morphological alterations in inner HCs. This deletion also altered gene expression, delaying downregulation of genes expressed in immature OHCs, including the actin regulator-encoding gene Coro2a , and accelerating upregulation of genes expressed in mature OHCs. Deleting Coro2a in Casz1 mutant mice restored F-actin density in cuticular plates but increased stereocilia bundle disorganization and hearing thresholds, revealing that CORO2A provides an overall beneficial effect. Our data indicate that CASZ1 regulates transcriptional and morphological maturation of OHCs, and that CASZ1 in maturing HCs is necessary for hearing.

iScienceVol. 29(9)
University of Iowa (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Cochlear (United States) (US), National Institute on Deafness and Other Communication Disorders (US)
National Institute on Deafness and Other Communication Disorders
Gender equality
Openalex Percentile: Top 13%
Hearing, Cochlea, Tinnitus, Genetics
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