KU Leuven, Forensic Biomedical Sciences, Department of Imaging & Pathology, Leuven, Belgium.
KU Leuven, Forensic Biomedical Sciences, Department of Imaging & Pathology, Leuven, Belgium.
Forensic Sci Int Genet. 2018 May;34:1-10. doi: 10.1016/j.fsigen.2018.01.005. Epub 2018 Jan 17.
Knowledge of Y-chromosomal short tandem repeat (Y-STR) mutation rates is essential to determine the most recent common ancestor (MRCA) in familial searching or genealogy research. Up to now, locus-specific mutation rates have been extensively examined especially for commercially available forensic Y-STRs, while haplogroup specific mutation rates have not yet been investigated in detail. Through 450 patrilineally related namesakes distributed over 212 deep-rooting genealogies, the individual mutation rates of 42 Y-STR loci were determined, including 27 forensic Y-STR loci from the Yfiler Plus kit and 15 additional Y-STR loci (DYS388, DYS426, DYS442, DYS447, DYS454, DYS455, DYS459a/b, DYS549, DYS607, DYS643, DYS724a/b and YCAIIa/b). At least 726 mutations were observed over 148,596 meiosis and individual Y-STR mutation rates varied from 2.83 × 10 to 1.86 × 10. The mutation rate was significantly correlated with the average allele size, the complexity of the repeat motif sequence and the age of the father. Significant differences in average Y-STR mutations rates were observed when haplogroup 'I & J' (4.03 × 10 mutations/generation) was compared to 'R1b' (5.35 × 10 mutations/generation) and to the overall mutation rate (5.03 × 10 mutations/generation). A difference in allele size distribution was identified as the only cause for these haplogroup specific mutation rates. The haplogroup specific mutation rates were also present within the commercially available Y-STR kits (Yfiler, PowerPlex Y23 System and Yfiler Plus). This observation has consequences for applications where an average Y-STR mutation rate is used, e.g. tMRCA estimations in familial searching and genealogy research.
Y 染色体短串联重复序列(Y-STR)突变率的知识对于确定家族搜索或系谱研究中的最近共同祖先(MRCA)至关重要。到目前为止,已经广泛研究了特定于基因座的突变率,特别是对于商业上可用的法医 Y-STR,而尚未详细研究单倍群特异性突变率。通过分布在 212 个深根系系谱中的 450 个直系同名男性,确定了 42 个 Y-STR 基因座的个体突变率,其中包括来自 Yfiler Plus 试剂盒的 27 个法医 Y-STR 基因座和 15 个额外的 Y-STR 基因座(DYS388、DYS426、DYS442、DYS447、DYS454、DYS455、DYS459a/b、DYS549、DYS607、DYS643、DYS724a/b 和 YCAIIa/b)。在 148596 次减数分裂中观察到至少 726 次突变,个体 Y-STR 突变率从 2.83×10到 1.86×10不等。突变率与平均等位基因大小、重复序列模体序列的复杂性和父亲的年龄显著相关。当 haplogroup 'I & J'(4.03×10 突变/代)与 haplogroup 'R1b'(5.35×10 突变/代)和总体突变率(5.03×10 突变/代)相比时,观察到平均 Y-STR 突变率存在显著差异。发现等位基因大小分布的差异是这些单倍群特异性突变率的唯一原因。这些单倍群特异性突变率也存在于商业上可用的 Y-STR 试剂盒(Yfiler、PowerPlex Y23 系统和 Yfiler Plus)中。这种观察结果对于应用具有平均 Y-STR 突变率的应用具有影响,例如在家族搜索和系谱研究中的 tMRCA 估计。