科尔蒂器官
耳蜗
连接蛋白
细胞生物学
抄写(语言学)
转录调控
生物
转录因子
基因
调节器
缝隙连接
听力损失
功能(生物学)
毛细胞
细胞内
核心
耳蜗核
损失函数
基因表达调控
神经科学
内耳
遗传学
遗传筛选
核蛋白
细胞核
串扰
感音神经性聋
基因表达
细胞
转录活性
作者
Xiaozhou Liu,Le Xie,Yuan Jin,S. Chen,Xinyu Shi,Yanjun Zong,Zhengdong Zhao,Weijia Kong,Yu Sun
标识
DOI:10.1002/advs.202514136
摘要
Gap junction Beta 2 Protein (GJB2, Connexin26, Cx26), the primary genetic cause of hereditary hearing loss (25%-50% of cases), has been exclusively regarded as forming an intercellular channel that mediates rapid communication. Here, we redefine its biological role by discovering its nuclear localization and direct transcriptional regulatory function in cochlear structure development. We demonstrate that Cx26 could aggregate in the nucleus of cochlear support cell and cell lines. Cx26 can bind to the promoter transcription start point of genomic DNA and directly regulate gene transcription, thus controlling the structural development of the tunnel of Corti during cochlear development. Further, we provide strategies based on mechanisms to promote the TC development and hearing rescue in Cx26 deficient cochlea, which has important implications for the discovery and development of treatment strategies for hearing loss caused by Cx26 deficiency.
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