一个新型的COCH p.D544Vfs*3 与DFNA9相关的变体 感神经听力损失 导致病态多重体科克林形成
Yingqiu Peng1,2, Mengya Xiang1,2, Ting Fan1,2
1ENT Institute and Department of Otorhinolaryngology, EYE & ENT Hospital, Fudan University, Shanghai 200031, China.
Life (Basel, Switzerland)
|January 23, 2024
概括
在COCH基因的新奇突变导致听力损失通过增加可林多元化. 这一发现扩大了对DFNA9的理解,将COCH变体与感应神经神经听力损失与最小的前庭问题联系起来.
科学领域:
- 遗传学 是一个遗传学.
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 分子生物学分子生物学
背景情况:
- 自体主导非综合征性听力损失通常与COCH基因的突变有关.
- DFNA9的特征是渐进的听力损失和可变的前庭功能障碍,与COCH变体相关.
研究的目的:
- 在一个听力障碍的中国家庭中识别和描述一种新的COCH变异.
- 调查鉴定变种影响可林功能的分子机制,并对DFNA9.9作出贡献.
主要方法:
- 对受影响的家庭成员进行了全面的听力测试和前庭功能测试.
- 使用下一代测序和桑格测序来识别和确认COCH变种.
- 进行了分子建模和基于细胞的过度表达研究 (HEK 293T细胞),以分析该变体对可克林的影响.
主要成果:
- 一种新的COCH变体 (c.1687delA,p.D544Vfs*3) 被确定并与家族中的听力损伤隔离.
- 该变种位于vWFA2域外,预计会破坏林后翻译裂变.
- 过度表达的研究表明,p.D544Vfs*3变体导致多重体林的形成增加.
结论:
- 新的COCH变异p.D544Vfs*3扩大了已知的DFNA9引起突变的范围.
- 导致可克林多元化的变种可能与DFNA9中的感觉神经听力损失有关,可能与较不严重的前庭症状有关.
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