King's College London, London 164651, U.K.
Emerg Top Life Sci. 2021 Sep 24;5(3):415-426. doi: 10.1042/ETLS20210204.
Genetic analysis of mitochondrial DNA (mtDNA) has always been a useful tool for forensic geneticists, mainly because of its ubiquitous presence in biological material, even in the absence of nuclear DNA. Sequencing, however, is not a skill that is part of the routine forensic analysis because of the relative rarity of requests, and the need for retention of necessary skill sets and associated accreditation issues. While standard Sanger sequencing may be relatively simple, many requests are made in the face of compromised biological samples. Newer technologies, provided through massively parallel sequencing (MPS), will increase the opportunity for scientists to include this tool in their routine, particularly for missing person investigations. MPS has also enabled a different approach to sequencing that can increase sensitivity in a more targeted approach. In these circumstances it is likely that only a laboratory that specialises in undertaking forensic mtDNA analysis will be able to take these difficult cases forward, more so because reviews of the literature have revealed significantly high levels of typing errors in publications reporting mtDNA sequences. The forensic community has set out important guidelines, not only in the practical aspects of analysis, but also in the interpretation of that sequence to ensure that accurate comparisons can be made. Analysis of low-level, compromised and ancient DNA is not easy, however, as contamination is extremely difficult to eliminate and circumstances leading to sequencing errors are all too easily introduced. These problems, and solutions, are discussed in the article in relation to several historic cases.
线粒体 DNA(mtDNA)的遗传分析一直是法医遗传学家的有用工具,主要是因为它在生物材料中无处不在,即使没有核 DNA 也是如此。然而,由于请求相对较少,并且需要保留必要的技能集和相关的认证问题,因此测序并不是常规法医分析的一部分技能。虽然标准的 Sanger 测序可能相对简单,但面对受损的生物样本,许多请求都会提出。通过大规模平行测序(MPS)提供的新技术将增加科学家将此工具纳入其常规工作的机会,特别是在失踪人员调查中。MPS 还实现了一种不同的测序方法,可以通过更有针对性的方法提高灵敏度。在这些情况下,可能只有专门从事法医 mtDNA 分析的实验室才能处理这些困难的案例,因为对文献的审查表明,在报告 mtDNA 序列的出版物中,类型错误率非常高。法医界不仅在分析的实际方面,而且在解释该序列方面都制定了重要的准则,以确保可以进行准确的比较。然而,分析低水平、受损和古老的 DNA 并不容易,因为污染极难消除,并且测序错误的情况很容易引入。本文讨论了与几个历史案例相关的这些问题及解决方案。