Xia Xingyu, Jiao Kexin, Hu Chaoping, Cheng Nachuan, Gao Mingshi, Xiong Shiyi, Wang Ningning, Zhu Bochen, Diao Meining, Yue Dongyue, Xi Jianying, Zhao Chongbo, Chen Chengwen, Zhu Wenhua
Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
Huashan Rare Disease Center, Shanghai Medical College, Huashan Hospital, Fudan University, Shanghai, China.
J Hum Genet. 2025 Jun 30. doi: 10.1038/s10038-025-01361-x.
Aberrant inclusion of pseudoexons (PE) in mature mRNA is a rare splicing defect contributing to Duchenne muscular dystrophy (DMD) pathogenesis. In this study, we described two affected males from a Chinese family who presented with progressive muscle weakness, elevated creatine kinase (CK) levels, and dystrophic changes on muscle pathology. Whole-genome sequencing followed by linkage-based filtering identified a shared deep intronic variant in intron 47 of DMD gene (c.6913-4037T>G), which activated a cryptic splice site and resulted in the inclusion of a 72 bp PE between exons 47 and 48. Patient induced pluripotent stem cells (iPSCs)-derived myotubes from the patient confirmed the presence of this PE, with a significant reduction in dystrophin expression compared to controls. Quantitative PCR revealed that aberrant transcripts comprised ~89% of total DMD transcripts in myotubes and ~97% in muscle, correlating with near-complete loss of dystrophin. Functional assays further showed impaired myotube fusion and altered calcium signaling. This study underscores the diagnostic complexity of intronic DMD variants and provides evidence supporting the pathogenicity of c.6913-4037T>G.
成熟mRNA中异常包含假外显子(PE)是一种罕见的剪接缺陷,与杜氏肌营养不良症(DMD)的发病机制有关。在本研究中,我们描述了来自一个中国家庭的两名患病男性,他们表现出进行性肌肉无力、肌酸激酶(CK)水平升高以及肌肉病理学上的营养不良性改变。全基因组测序后基于连锁的筛选在DMD基因第47内含子中鉴定出一个共享的深度内含子变异(c.6913-4037T>G),该变异激活了一个隐蔽剪接位点,导致在第47和48外显子之间包含一个72bp的PE。来自患者的诱导多能干细胞(iPSC)衍生的肌管证实了该PE的存在,与对照组相比,肌营养不良蛋白表达显著降低。定量PCR显示,异常转录本在肌管中占总DMD转录本的约89%,在肌肉中占约97%,这与肌营养不良蛋白几乎完全缺失相关。功能分析进一步表明肌管融合受损和钙信号改变。本研究强调了内含子DMD变异的诊断复杂性,并提供了支持c.6913-4037T>G致病性的证据。