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首页> 外文期刊>International journal of legal medicine >Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR Yfiler PCR amplification kit.
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Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR Yfiler PCR amplification kit.

机译:AmpFlSTR Yfiler PCR扩增试剂盒中包含的17个Y染色体短串联重复序列多态性的全面突变分析。

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摘要

The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpFlSTR Yfiler polymerase chain reaction amplification kit have become widely used for forensic and evolutionary applications where a reliable knowledge on mutation properties is necessary for correct data interpretation. Therefore, we investigated the 17 Yfiler Y-STRs in 1,730-1,764 DNA-confirmed father-son pairs per locus and found 84 sequence-confirmed mutations among the 29,792 meiotic transfers covered. Of the 84 mutations, 83 (98.8%) were single-repeat changes and one (1.2%) was a double-repeat change (ratio, 1:0.01), as well as 43 (51.2%) were repeat gains and 41 (48.8%) repeat losses (ratio, 1:0.95). Medians from Bayesian estimation of locus-specific mutation rates ranged from 0.0003 for DYS448 to 0.0074 for DYS458, with a median rate across all 17 Y-STRs of 0.0025. The mean age (at the time of son's birth) of fathers with mutations was with 34.40 (+/-11.63) years higher than that of fathers without ones at 30.32 (+/-10.22) years, a difference that is highly statistically significant (p < 0.001). A Poisson-based modeling revealed that the Y-STR mutation rate increased with increasing father's age on a statistically significant level (alpha = 0.0294, 2.5% quantile = 0.0001). From combining our data with those previously published, considering all together 135,212 meiotic events and 331 mutations, we conclude for the Yfiler Y-STRs that (1) none had a mutation rate of >1%, 12 had mutation rates of >0.1% and four of <0.1%, (2) single-repeat changes were strongly favored over multiple-repeat ones for all loci but 1 and (3) considerable variation existed among loci in the ratio of repeat gains versus losses. Our finding of three Y-STR mutations in one father-son pair (and two pairs with two mutations each) has consequences for determining the threshold of allelic differences to conclude exclusion constellations in future applications of Y-STRs in paternity testing and pedigree analyses.
机译:AmpFlSTR Yfiler聚合酶链反应扩增试剂盒中包含的Y染色体短串联重复序列(Y-STR)多态性已广泛用于法医学和进化应用,在这些应用中,对突变特性的可靠了解对于正确的数据解释是必需的。因此,我们调查了每个基因座的1,730-1,764个DNA确认的父子对中的17个Yfiler Y-STR,发现了29,792个减数分裂转移中的84个序列确认的突变。在这84个突变中,有83个(98.8%)是单重复改变,一个(1.2%)是双重复改变(比例为1:0.01),还有43个(51.2%)是重复获得和41个(48.8) %)重复损失(比例为1:0.95)。贝叶斯估计的基因座特异性突变率的中位数范围从DYS448的0.0003到DYS458的0.0074,所有17个Y-STR的中位数为0.0025。具有突变的父亲的平均年龄(在儿子出生时)比没有父亲的父亲的平均年龄高30.32(+/- 10.22)岁,高34.40(+/- 11.63)岁,这一差异具有统计学意义( p <0.001)。基于Poisson的模型显示,Y-STR突变率随着父亲年龄的增加而增加,具有统计学上的显着水平(α= 0.0294,2.5%的分位数= 0.0001)。通过将我们的数据与先前发表的数据相结合,综合考虑135,212次减数分裂事件和331个突变,我们得出Yfiler Y-STR的结论是:(1)没有一个突变率> 1%,有12个突变率> 0.1%,并且<0.1%中的四个,(2)对于所有基因座,单重复变化都比多重复变化更受青睐,但1和(3)在基因座之间,重复增益与损失的比例存在相当大的差异。我们在一对父子对中发现了三个Y-STR突变(以及两对分别具有两个突变),这对确定等位基因差异的阈值具有重要意义,从而可以在将来在亲子鉴定和血统分析中应用Y-STR时得出排除星座。

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