Department of Forensic Molecular Biology, Erasmus University Medical Center Rotterdam, The Netherlands.
Am J Hum Genet. 2010 Sep 10;87(3):341-53. doi: 10.1016/j.ajhg.2010.08.006.
Nonrecombining Y-chromosomal microsatellites (Y-STRs) are widely used to infer population histories, discover genealogical relationships, and identify males for criminal justice purposes. Although a key requirement for their application is reliable mutability knowledge, empirical data are only available for a small number of Y-STRs thus far. To rectify this, we analyzed a large number of 186 Y-STR markers in nearly 2000 DNA-confirmed father-son pairs, covering an overall number of 352,999 meiotic transfers. Following confirmation by DNA sequence analysis, the retrieved mutation data were modeled via a Bayesian approach, resulting in mutation rates from 3.78 × 10(-4) (95% credible interval [CI], 1.38 × 10(-5) - 2.02 × 10(-3)) to 7.44 × 10(-2) (95% CI, 6.51 × 10(-2) - 9.09 × 10(-2)) per marker per generation. With the 924 mutations at 120 Y-STR markers, a nonsignificant excess of repeat losses versus gains (1.16:1), as well as a strong and significant excess of single-repeat versus multirepeat changes (25.23:1), was observed. Although the total repeat number influenced Y-STR locus mutability most strongly, repeat complexity, the length in base pairs of the repeated motif, and the father's age also contributed to Y-STR mutability. To exemplify how to practically utilize this knowledge, we analyzed the 13 most mutable Y-STRs in an independent sample set and empirically proved their suitability for distinguishing close and distantly related males. This finding is expected to revolutionize Y-chromosomal applications in forensic biology, from previous male lineage differentiation toward future male individual identification.
非重组 Y 染色体微卫星(Y-STR)广泛用于推断种群历史、发现谱系关系以及为刑事司法目的识别男性。尽管其应用的一个关键要求是可靠的可变性知识,但迄今为止,只有少数 Y-STR 具有经验数据。为了解决这个问题,我们分析了近 2000 对 DNA 确认的父子对中的大量 186 个 Y-STR 标记,总共涵盖了 352999 次减数分裂传递。经过 DNA 序列分析确认后,通过贝叶斯方法对检索到的突变数据进行建模,得出的突变率为 3.78×10(-4)(95%可信区间[CI],1.38×10(-5) - 2.02×10(-3))至 7.44×10(-2)(95% CI,6.51×10(-2) - 9.09×10(-2))/每个标记/代。在 120 个 Y-STR 标记的 924 个突变中,观察到重复损失与增益的非显著过剩(1.16:1),以及单重复与多重复变化的强烈且显著过剩(25.23:1)。虽然总重复数对 Y-STR 基因座的可变性影响最大,但重复复杂性、重复基序的碱基对长度以及父亲的年龄也对 Y-STR 的可变性有影响。为了举例说明如何实际利用这些知识,我们在一个独立的样本集中分析了 13 个最易变的 Y-STR,并通过经验证明了它们适合区分近亲和远亲男性。这一发现有望使法医生物学中的 Y 染色体应用从之前的男性谱系分化转向未来的男性个体识别。