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Mutation Rate at Commonly Used Forensic STR Loci: Paternity Testing Experience

机译:常用法医STR位点的突变率:亲子鉴定经验

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摘要

Paternity tests are carried out by the analysis of hypervariable short tandem repeat DNA loci. These microsatellite sequences mutate at a higher rate than that of bulk DNA. The occurrence of germline mutations at STR loci posses problems in interpretation of resulting genetic profiles. We recently analyzed 59–159 parent/child allele transfers at 13 microsatellite loci. We identified 12 mutations in 7 microsatellite loci. No mutations were occurred in other 6 loci. The highest mutation rate was observed with 5 mutations at D8S1179 locus at different alleles. The event was always single repeat related. The mutation rate was between 0 and 1.5 x 10-2per locus per gamete per generation. The mutation event is very crucial for forensic DNA testing and accumulation of STR mutation data is extremely important for genetic profile interpretation.
机译:通过分析高变短串联重复DNA基因座来进行亲子鉴定。这些微卫星序列的突变速率要高于整体DNA的突变速率。 STR基因座上种系突变的发生在解释所得的遗传概况方面存在问题。我们最近分析了13个微卫星基因座上59-159个亲子等位基因转移。我们在7个微卫星基因座中鉴定出12个突变。在其他6个基因座中没有发生突变。在D8S1179位点的5个突变处,等位基因的突变率最高。该事件总是与单个重复相关。每一代每配子的突变率在0和1.5×10-2个位点之间。突变事件对于法医DNA测试非常关键,而STR突变数据的积累对于遗传图谱解释极为重要。

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