Forensic Research Laboratory, Centre of Excellence in Molecular Biology, University of the Punjab, Lahore 53700, Pakistan.
Centre for Forensic Science, University of Technology Sydney, Sydney 2007, Australia.
Genes (Basel). 2022 May 26;13(6):946. doi: 10.3390/genes13060946.
Rapidly mutating Y-chromosomal short tandem repeats (RM Y STRs) with mutation rates ≥ 10 per locus per generation are valuable for differentiating amongst male paternal relatives where standard Y STRs with mutation rates of ≤10 per locus per generation may not. Although the 13 RM Y STRs commonly found in commercial assays provide higher levels of paternal lineage differentiation than conventional Y STRs, there are many male paternal relatives that still cannot be differentiated. This can be improved by increasing the number of Y STRs or choosing those with high mutation rates. We present a RM Y STR multiplex comprising 19 loci with high mutation rates and its developmental validation (repeatability, sensitivity and male specificity). The multiplex was found to be robust, reproducible, specific and sensitive enough to generate DNA profiles from samples with inhibitors. It was also able to detect all contributor alleles of mixtures in ratios up to 9:1. We provide preliminary evidence for the ability of the multiplex to discriminate between male paternal relatives by analyzing large numbers of male relative pairs (536) separated by one to seven meioses. A total of 96 mutations were observed in 162 meioses of father-son pairs, and other closely related male pairs were able to be differentiated after 1, 2, 3, 4, 5, 6 and 7 meiosis in 44%, 69%, 68%, 85%, 0%, 100% and 100% of cases, respectively. The multiplex offers a noticeable enhancement in the ability to differentiate paternally related males compared with the 13 RM Y STR set. We envision the future application of our 19 RM Yplex in criminal cases for the exclusion of male relatives possessing matching standard Y STR profiles and in familial searching with unknown suspects. It represents a step towards the complete individualization of closely related males.
快速突变的 Y 染色体短串联重复序列(RM Y STR)具有≥10 个每个基因座每代的突变率,对于区分男性父系亲属非常有用,而标准 Y STR 的突变率≤10 个每个基因座每代则可能无法区分。虽然商业检测中常见的 13 个 RM Y STR 提供了比传统 Y STR 更高水平的父系血统分化,但仍有许多男性父系亲属无法区分。通过增加 Y STR 的数量或选择具有高突变率的 Y STR 可以改善这种情况。我们提出了一个包含 19 个高突变率基因座的 RM Y STR 多重扩增试剂盒,并对其进行了开发验证(重复性、灵敏度和雄性特异性)。该多重扩增试剂盒被发现稳健、可重复、特异性和灵敏度都很高,足以从有抑制剂的样本中生成 DNA 图谱。它还能够检测到高达 9:1 比例的混合贡献等位基因。我们通过分析大量通过 1 到 7 次减数分裂分离的男性亲属对(536 对),提供了该多重扩增试剂盒区分男性父系亲属的初步证据。在父亲-儿子对的 162 次减数分裂中观察到了 96 个突变,并且在 44%、69%、68%、85%、0%、100%和 100%的情况下,能够区分其他密切相关的男性对在 1、2、3、4、5、6 和 7 次减数分裂后。与 13 个 RM Y STR 集相比,该多重扩增试剂盒在区分父系亲属方面的能力有明显提高。我们设想未来将我们的 19 个 RM Yplex 应用于刑事案件中,排除具有匹配标准 Y STR 图谱的男性亲属,并用于与未知嫌疑人的家族搜索。这代表着朝着密切相关男性个体完全个体化迈出的一步。