ZBTB20 is essential for cochlear maturation and hearing in mice

Author:

Xie Zhifang12ORCID,Ma Xian-Hua2ORCID,Bai Qiu-Fang3ORCID,Tang Jie4ORCID,Sun Jian-He5,Jiang Fei1ORCID,Guo Wei5ORCID,Wang Chen-Ma3ORCID,Yang Rui2,Wen Yin-Chuan4,Wang Fang-Yuan5,Chen Yu-Xia2ORCID,Zhang Hai2,He David Z.6ORCID,Kelley Matthew W.7,Yang Shiming5ORCID,Zhang Weiping J.23ORCID

Affiliation:

1. Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Institute of Early Life Health, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092, China

2. Department of Pathophysiology, Naval Medical University, Shanghai 200433, China

3. NHC Key Laboratory of Hormones and Development, Chu Hsien-I Memorial Hospital and Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China

4. Department of Physiology, Southern Medical University, Guangzhou, Guangdong 510515, China

5. Senior Department of Otolaryngology-Head and Neck Surgery, National Clinical Research Center for Otolaryngologic Diseases, the Sixth Medical Center of PLA General Hospital, Beijing 100141, China

6. Department of Biomedical Sciences, Creighton University School of Medicine, Omaha, NE 68178

7. NIDCD, Porter Neuroscience Research Center, Bethesda, MD 20892

Abstract

The mammalian cochlear epithelium undergoes substantial remodeling and maturation before the onset of hearing. However, very little is known about the transcriptional network governing cochlear late-stage maturation and particularly the differentiation of its lateral nonsensory region. Here, we establish ZBTB20 as an essential transcription factor required for cochlear terminal differentiation and maturation and hearing. ZBTB20 is abundantly expressed in the developing and mature cochlear nonsensory epithelial cells, with transient expression in immature hair cells and spiral ganglion neurons. Otocyst-specific deletion of Zbtb20 causes profound deafness with reduced endolymph potential in mice. The subtypes of cochlear epithelial cells are normally generated, but their postnatal development is arrested in the absence of ZBTB20, as manifested by an immature appearance of the organ of Corti, malformation of tectorial membrane (TM), a flattened spiral prominence (SP), and a lack of identifiable Boettcher cells. Furthermore, these defects are related with a failure in the terminal differentiation of the nonsensory epithelium covering the outer border Claudius cells, outer sulcus root cells, and SP epithelial cells. Transcriptome analysis shows that ZBTB20 regulates genes encoding for TM proteins in the greater epithelial ridge, and those preferentially expressed in root cells and SP epithelium. Our results point to ZBTB20 as an essential regulator for postnatal cochlear maturation and particularly for the terminal differentiation of cochlear lateral nonsensory domain.

Funder

Ministry of Science and Technology of the People's Republic of China

MOST | National Natural Science Foundation of China

Shanghai Municipal Health Commission of Chian

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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