在COQ4基因中的双变异导致遗传性性,主要的表型
Qiao Wei1, Hao Yu1, Pei-Shan Wang1
1Department of Medical Genetics and Center for Rare Diseases, and Department of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
CNS neuroscience & therapeutics
|November 28, 2023
概括
在遗传性性 (HSP) 患者中发现了COQ4基因的遗传变异. 这一发现扩大了已知的COQ4相关疾病及其相关表型的范围.
科学领域:
- 神经遗传学 神经遗传学
- 线粒体生物学 线粒体生物学
- 神经学 神经学
背景情况:
- 遗传性性 (HSP) 是一种影响上部运动神经元的神经退行性疾病.
- COQ4基因变异与原发性CoQ10缺乏-7 (COQ10D7) 相关,这是一种线粒体疾病.
研究的目的:
- 查COQ4变异在一组患者的基因未确定的HSP.
- 调查COQ4变异在HSP病因学中的作用.
主要方法:
- 在87名HSP指数患者及其家属身上进行了整体外基因组测序 (WES).
- 在患者衍生的纤维细胞系上进行了功能性研究,以评估变体的致病性.
主要成果:
- 在中国的三种高杆菌血统中发现了五种COQ4变异,其中包括两种新型变异 (c.87dupT和c.304C>T).
- 该研究描述了COQ4变体引起的早期发病的纯HSP的第一个病例.
- 功能性研究表明,患者细胞中的细胞CoQ10水平降低,线粒体结构异常.
结论:
- COQ4基因的双边变异可以导致HSP占主导地位的表型.
- 这些发现扩大了COQ4相关疾病的表型谱.
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