Department of Forensic Molecular Biology, Erasmus MC University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands.
Forensic Sci Int Genet. 2012 Mar;6(2):208-18. doi: 10.1016/j.fsigen.2011.04.017. Epub 2011 May 25.
The panels of 9-17 Y-chromosomal short tandem repeats (Y-STRs) currently used in forensic genetics have adequate resolution of different paternal lineages in many human populations, but have lower abilities to separate paternal lineages in populations expressing low Y-chromosome diversity. Moreover, current Y-STR sets usually fail to differentiate between related males who belong to the same paternal lineage and, as a consequence, conclusions cannot be drawn on the individual level as is desirable for forensic interpretations. Recently, we identified a new panel of rapidly mutating (RM) Y-STRs, composed of 13 markers with mutation rates above 1 × 10(-2), whereas most Y-STRs, including all currently used in forensics, have mutation rates in the order of 1 × 10(-3) or lower. In the present study, we demonstrate in 604 unrelated males sampled from 51 worldwide populations (HGDP-CEPH) that the RM Y-STRs provide substantially higher haplotype diversity and haplotype discrimination capacity (with only 3 haplotypes shared between 8 of the 604 worldwide males), than obtained with the largest set of 17 currently used Y-STRs (Yfiler) in the same samples (33 haplotypes shared between 85 males). Hence, RM Y-STRs yield high-resolution paternal lineage differentiation and provide a considerable improvement compared to Yfiler. We also find in this worldwide dataset substantially less genetic population substructure within and between geographic regions with RM Y-STRs than with Yfiler Y-STRs. Furthermore, with the present study we provide enhanced data evidence that the RM Y-STR panel is extremely successful in differentiating between closely and distantly related males. Among 305 male relatives, paternally connected by 1-20 meiotic transfers in 127 independent pedigrees, we show that 66% were separated by mutation events with the RM Y-STR panel whereas only 15% were with Yfiler; hence, RM Y-STRs provide a statistically significant 4.4-fold increase of average male relative differentiation relative to Yfiler. The RM Y-STR panel is powerful enough to separate closely related males; nearly 50% of the father and sons, and 60% of brothers could be distinguished with RM Y-STRs, whereas only 7.7% and 8%, respectively, with Yfiler. Thus, by introducing RM Y-STRs to the forensic genetic community we provide important solutions to several of the current limitations of Y chromosome analysis in forensic genetics.
目前在法医遗传学中使用的 9-17 个 Y 染色体短串联重复序列(Y-STRs)面板在许多人群中具有足够的分辨率,可以区分不同的父系血统,但在表达低 Y 染色体多样性的人群中,其分离父系血统的能力较低。此外,目前的 Y-STR 组通常无法区分属于同一父系血统的相关男性,因此,无法像法医解释所期望的那样在个体水平上得出结论。最近,我们鉴定了一组新的快速突变(RM)Y-STRs,由 13 个突变率高于 1×10(-2)的标记组成,而大多数 Y-STRs,包括目前在法医中使用的所有 Y-STRs,其突变率都在 1×10(-3)或更低。在本研究中,我们在来自 51 个世界人群(HGDP-CEPH)的 604 个无关男性中证明,RM Y-STRs 提供了更高的单倍型多样性和单倍型区分能力(在 604 个世界男性中,只有 3 个单倍型在 8 个男性中共享),而在相同样本中使用的最大一组 17 个当前使用的 Y-STRs(Yfiler)获得的单倍型多样性和单倍型区分能力(在 85 个男性中共享 33 个单倍型)要高得多。因此,RM Y-STRs 可实现高分辨率的父系血统分化,与 Yfiler 相比有了很大的改进。我们还在这个全球数据集内发现,使用 RM Y-STRs 的遗传群体结构比使用 Yfiler Y-STRs 的遗传群体结构要少得多,而且在地理区域之间也是如此。此外,通过本研究,我们提供了增强的数据证据,证明 RM Y-STR 面板在区分密切和遥远相关的男性方面非常成功。在 305 名男性亲属中,通过 127 个独立谱系中的 1-20 次减数分裂连接,我们发现,66%的男性通过 RM Y-STR 面板的突变事件得以区分,而只有 15%的男性通过 Yfiler 得以区分;因此,RM Y-STRs 提供了 4.4 倍的男性亲属平均分化的统计学显著增加,相对于 Yfiler。RM Y-STR 面板功能强大,足以区分密切相关的男性;近 50%的父子和 60%的兄弟可以用 RM Y-STRs 区分,而只有 Yfiler 分别为 7.7%和 8%。因此,通过向法医遗传学界引入 RM Y-STRs,我们为法医遗传学中 Y 染色体分析的当前几个局限性提供了重要的解决方案。