在一个患有综合征性神经发育障碍的家族中识别和功能分析一种新的SMARCC2拼接变异
Ming Li1,2,3, Jingqi Lin1,2,3, Hongjun Fei1,2,3
1The International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030, China.
Orphanet journal of rare diseases
|February 3, 2025
概括
在SMARCC2基因中,一种新的拼接变异在成年男性双胞胎中引起了综合征性神经发育障碍. 与其他变异类型相比,这种SMARCC2变异导致更严重的神经现象.
科学领域:
- 遗传学 遗传学 是一个
- 神经发育障碍 神经发育障碍
- 分子生物学分子生物学
背景情况:
- 神经发育障碍 (NDD) 是一种复杂的遗传疾病.
- 在人类发育中,SMARCC2基因起着至关重要的作用.
- 识别新型变异及其致病机制对于理解NDD至关重要.
研究的目的:
- 为了确定一种新型SMARCC2拼接变异的致病性,该变异在患有NDD的双胞胎中发现.
- 为了研究SMARCC2变种的基因型-表型特征.
主要方法:
- 整体外体测序 (WES) 和桑格测序用于变种识别和验证.
- 反转录PCR (RT-PCR) 和TA-克隆测序用于分析mRNA拼接.
- 临床数据收集和与以前报告的病例进行比较.
主要成果:
- 在患有NDD的单胞胎双胞胎中发现了一种新型异质合体SMARCC2拼接变体 (c.1496+1G>T).
- 这种变异导致异常拼接,导致SMARCC2mRNA中的表子16在框架内插入或删除.
- 结构分析表明,这些变化破坏了蛋白质的二次结构.
- 患有这种框架内变异的患者表现出比患有截断变异的患者更严重的神经现象.
结论:
- 一种新的SMARCC2拼接变体是致病的,在受影响的双胞胎中引起综合征性NDD.
- 在SMARCC2中的误解/框架变异与更严重的神经现象型有关.
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