Department of Neurology, Peking University First Hospital, Beijing, 100034, China.
GrandOmics Biosciences, Beijing, China.
Ann Clin Transl Neurol. 2020 Oct;7(10):2041-2046. doi: 10.1002/acn3.51201. Epub 2020 Sep 20.
The precise genetic diagnosis of dystrophinopathies can be challenging, largely due to rare deep intronic variants and more complex structural variants (SVs). We report on the genetic characterization of a dystrophinopathy patient. He remained without a genetic diagnosis after routine genetic testing, dystrophin protein and mRNA analysis, and short- and long-read whole DMD gene sequencing. We finally identified a novel complex SV in DMD via long-read whole-genome sequencing. The variant consists of a large-scale (~1Mb) inversion/deletion-insertion rearrangement mediated by LINE-1s. Our study shows that long-read whole-genome sequencing can serve as a clinical diagnostic tool for genetically unsolved dystrophinopathies.
肌营养不良蛋白病的精确基因诊断具有挑战性,主要是由于罕见的深内含子变异和更复杂的结构变异(SVs)。我们报告了一例肌营养不良蛋白病患者的基因特征。经过常规基因检测、肌营养不良蛋白和 mRNA 分析以及短读长和长读长全 DMD 基因测序,他仍未得到基因诊断。我们最终通过长读长全基因组测序鉴定了 DMD 中的一种新型复杂 SV。该变异由 LINE-1s 介导的大规模(~1Mb)倒位/缺失-插入重排组成。我们的研究表明,长读长全基因组测序可作为遗传未解决的肌营养不良蛋白病的临床诊断工具。