Obal Marcel, Zupanič Pajnič Irena
Institute of Forensic Medicine, Faculty of Medicine, University of Ljubljana, Korytkova 2, Ljubljana, 1000, Slovenia.
Int J Legal Med. 2025 Sep 15. doi: 10.1007/s00414-025-03603-1.
Rapid technological advancements have significantly enhanced DNA analysis. A key innovation is Next-Generation Sequencing (NGS), also known as Massively Parallel Sequencing (MPS), which followed classic Sanger (CS) sequencing. Compared to CS, NGS offers higher sensitivity, resolution, and throughput, making it particularly valuable for mitochondrial DNA (mtDNA) analysis. The high copy number, matrilineal inheritance, and non-recombining nature of mtDNA, especially its hypervariable regions (HV), make it highly relevant in forensic investigations. NGS has introduced streamlined protocols and improved low-level heteroplasmy detection in mtDNA sequencing. However, with any new technology, its informativeness and authenticity must be evaluated against traditional methods. This study compared mitotypes from degraded WWII skeletal remains recovered from a Slovenian mass grave, using the same DNA extraction method to minimize pre-sequencing variability. Femurs were mechanically and chemically cleaned, pulverized, and fully demineralized. DNA was extracted and purified using EZ1 Advanced XL and quantified with an in-house protocol. CS sequencing was performed using BigDye Terminator Kit v1.1 and ABI PRISM™ 3130 Genetic Analyzer, while NGS was conducted with the Precision ID mtDNA Control Region Panel and Ion GeneStudio™ S5 System. Comparison of mitotypes revealed that NGS identified low-level heteroplasmies undetectable by CS, particularly in length heteroplasmy. However, since Ion Torrent™ Suite 5.10.1 is prone to errors, certain NGS variants had to be disregarded.
快速的技术进步显著提升了DNA分析水平。一项关键创新是下一代测序(NGS),也称为大规模平行测序(MPS),它是在经典桑格(CS)测序之后出现的。与CS相比,NGS具有更高的灵敏度、分辨率和通量,这使其在线粒体DNA(mtDNA)分析中特别有价值。mtDNA的高拷贝数、母系遗传和非重组性质,尤其是其高变区(HV),使其在法医调查中具有高度相关性。NGS在mtDNA测序中引入了简化的方案并改进了低水平异质性检测。然而,对于任何新技术,都必须根据传统方法评估其信息性和真实性。本研究比较了从斯洛文尼亚乱葬岗挖掘出的二战时期降解骨骼遗骸的线粒体类型,使用相同的DNA提取方法以尽量减少测序前的变异性。对股骨进行机械和化学清洁、粉碎并完全脱矿质。使用EZ1 Advanced XL提取和纯化DNA,并采用内部方案进行定量。使用BigDye Terminator Kit v1.1和ABI PRISM™ 3130遗传分析仪进行CS测序,而使用Precision ID mtDNA控制区面板和Ion GeneStudio™ S5系统进行NGS测序。线粒体类型的比较表明,NGS能够识别出CS无法检测到的低水平异质性,尤其是长度异质性。然而,由于Ion Torrent™ Suite 5.10.1容易出错,某些NGS变体不得不被忽略。