Leverhulme Research Centre for Forensic Science, Fleming Gym Building, University of Dundee, Small's Wynd, Dundee, United Kingdom.
Health Informatics Centre, Division of Population and Health Genomics, School of Medicine, University of Dundee, Dundee, United Kingdom.
Sci Justice. 2024 Sep;64(5):533-542. doi: 10.1016/j.scijus.2024.08.001. Epub 2024 Aug 5.
One of the most challenging issues still present in forensic DNA analysis is identifying individuals in samples containing DNA from multiple contributors. The introduction of novel identification markers may be a useful tool in the deconvolution of such DNA mixtures. In this study, we investigated the potential of alleles from the human leukocyte antigen system (HLA) to aid in identifying individuals in complex, multiple-donor DNA samples. The most advantageous characteristic of the HLA complex is its polymorphism in the human genome. A 22-loci multiplex with HLA markers was designed and applied to two-, three-, and four-person DNA mixtures. The results of the conducted experiments demonstrated that the identification of individuals in multiple contributor samples with the help of HLA markers is possible; however, it is clear that the reliability of the method is heavily dependent on the number of unique alleles for each individual in the analysed mixture. In order to compare this novel approach against the already established process, the same group of reference and multiple-contributor samples was analysed with a commonly used set of STR markers. This proof-of-concept research shows the importance of examining alternative solutions to the current deconvolution challenge in forensic DNA profiling.
在法医 DNA 分析中,仍然存在一个极具挑战性的问题,即识别包含多个供体 DNA 的样本中的个体。引入新的鉴定标记可能是解析此类 DNA 混合物的有用工具。在这项研究中,我们研究了人类白细胞抗原(HLA)系统中的等位基因在辅助识别复杂的多供体 DNA 样本中的个体方面的潜力。HLA 复合体最有利的特征是其在人类基因组中的多态性。设计并应用了一个包含 22 个 HLA 标记的 22 个基因座多重扩增试剂盒,对两人、三人及四人 DNA 混合物进行了分析。实验结果表明,借助 HLA 标记识别多供体样本中的个体是可行的;然而,很明显,该方法的可靠性在很大程度上取决于分析混合物中每个个体的独特等位基因数量。为了将这种新方法与已建立的方法进行比较,使用一组常用的 STR 标记对同一组参考样本和多供体样本进行了分析。这项概念验证研究表明,在法医 DNA 分析中,检查当前混合物解析挑战的替代解决方案非常重要。