期刊论文详细信息
Molecular Genetics & Genomic Medicine
Whole exome sequencing is an alternative method in the diagnosis of mitochondrial DNA diseases
Ruiguo Chen1  Yanyun Ma1  Shengyang Wu1  Junwu Liu1  Yuezhen Li1  Zhulin Yuan1  Jiasen Wang1  Chong Sun2 
[1] Berry Genomics Co., Ltd Beijing China;Department of Neurology, Huashan Hospital Fudan University Shanghai China;
关键词: genetic diagnosis;    mitochondrial disease;    next generation sequencing;    whole exome sequencing;   
DOI  :  10.1002/mgg3.1943
来源: DOAJ
【 摘 要 】

Abstract Background Mitochondrial disease (MD) is genetically a heterogeneous group of disorders with impairment in respiratory chain complexes or pathways associated with the mitochondrial function. Nowadays, it is still a challenge for the genetic screening of MD due to heteroplasmy of mitochondrial genome and the complex model of inheritance. This study was designed to investigate the feasibility of whole exome sequencing (WES)‐based testing as an alternative option for the diagnosis of MD. Methods A Chinese Han cohort of 48 patients with suspect MD features was tested using nanoWES, which was a self‐designed WES technique that covered the complete mtDNA genome and 21,019 nuclear genes. Fourteen patients were identified with a single genetic variant and three with single deletion in mtDNA. Results The heteroplasmy levels of variants in mitochondrial genome range from 11% to 100%. NanoWES failed to identify multiple deletions in mtDNA compared with long range PCR and massively parallel sequencing (LR‐PCR/MPS). However, our testing showed obvious advantages in identifying variations in nuclear DNA. Based on nanoWES, we identified two patients with nuclear DNA variation. One of them showed Xp22.33‐q28 duplication, which indicated a possibility of Klinefelter syndrome. Conclusion NanoWES yielded a diagnostic rate of 35.4% for MD. With the rapid advances of next generation sequencing technique and decrease in cost, we recommend the usage of nanoWES as a first‐line method in clinical diagnosis.

【 授权许可】

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