Gil Yongjin, Ryu Jiho, Yang Hayoung, Ma Yechan, Nam Ki-Hoan, Jang Sung-Wuk, Shim Sungbo
Department of Biochemistry, Chungbuk National University, Cheongju 28644, Republic of Korea.
Department of Biochemistry and Molecular Biology, Brain Korea 21 Project, Asan Medical Center, University of Ulsan College of Medicine, Seoul 138-736, Republic of Korea.
Int J Mol Sci. 2024 Nov 26;25(23):12700. doi: 10.3390/ijms252312700.
The inner ear is one of the sensory organs of vertebrates and is largely composed of the vestibule, which controls balance, and the cochlea, which is responsible for hearing. In particular, a problem in cochlear development can lead to hearing loss. Although numerous studies have been conducted on genes involved in the development of the cochlea, many areas still need to be discovered regarding factors that control the patterning of the early cochlear duct. Herein, based on the dynamic expression pattern of FOXG1 in the apical and basal regions of the E13.5 cochlear duct, we identified detailed expression regions through an open-source analysis of single-cell RNA analysis data and demonstrated a clinical correlation with hearing loss. The distinct expression patterns of FOXG1 and GATA3 during the patterning process of the cochlear duct provide important clues to understanding how the fates of the apical and basal regions are divided. These results are expected to be extremely important not only for understanding the molecular mechanisms involved in the early development of the cochlear duct, but also for identifying potential genes that cause hearing loss.
内耳是脊椎动物的感觉器官之一,主要由控制平衡的前庭和负责听力的耳蜗组成。特别是,耳蜗发育问题会导致听力损失。尽管已经对参与耳蜗发育的基因进行了大量研究,但在控制早期耳蜗管模式形成的因素方面,仍有许多领域有待探索。在此,基于FOXG1在E13.5耳蜗管顶端和基部区域的动态表达模式,我们通过对单细胞RNA分析数据的开源分析确定了详细的表达区域,并证明了其与听力损失的临床相关性。FOXG1和GATA3在耳蜗管模式形成过程中的不同表达模式为理解顶端和基部区域的命运如何划分提供了重要线索。这些结果不仅有望对于理解耳蜗管早期发育所涉及的分子机制极其重要,而且对于识别导致听力损失的潜在基因也极其重要。