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首页> 外文期刊>Forensic Medicine and Anatomy Research >Mutation Analysis of STR Locus on 23 Autosomes in Hainan Population
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Mutation Analysis of STR Locus on 23 Autosomes in Hainan Population

机译:海南人群23例纯弹性素的突变分析

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摘要

[Objective] To analyze the mutation signature and regularity of STR locus on 23 autosomes in paternity testing cases in Hainan. [Methods] A total of 2715 paternity testing cases accepted by the Forensic Medical Identification Centre of our hospital from 2017 to 2020 derived from counties and cities in Hainan Province were collected, the cases containing gene mutations were selected, the mutation rate and details of each locus were counted, and the mutation regu-larity of 23 STR loci was analyzed. [Results] Of the 2715 cases identified as “support”, 1487 were triplet cases and 1640 were dyad cases, totaling 4614 meioses; There were 50 gene mutation events (including 17 triplet mutations and 33 dyad mutations), with an average mutation rate of 0.0047% and a cumulative mutation rate of 1.0837%. A total of 19 of the 23 STR loci were mutated, with a mutation rate of 0.1301% at the D12S391 locus and 0.0217% at five loci, TPOX, D1S1656, D2S441, D22S1045, and PentaD, while no muta-tion events were found at four loci, D19S433, TH01, D13S317, and D7S820. Of the 50 mutation events, 47 were one-step mutations, 1 was two-step, and 2 were three-step. There were 35 paternal mutations (13 triplets and 22 dyads), 6 maternal mutations (4 triplets and 2 dyads), and 9 indeterminate pater-nal/maternal mutations, with a paternal to maternal mutation ratio of 5.83:1. [Conclusion] The mutation rate of D12S391 locus is the highest, and the muta-tion rate of TPOX, D1S1656, D2S441, D22S1045 and PentaD loci is the lowest in Hainan population, and paternal mutations are more than maternal muta-tions. In the paternity test, if 1 - 3 STR loci do not conform to the genetic law, especially when the mutant locus is homozygous or the next of kin is identi-fied, it is necessary to use other kits to review and increase the number of loci or use the second-generation sequencing technology to confirm, carefully de-termine the mutation and ensure the accuracy of the identification conclusion.
机译:[目的]分析海南第23例拷贝术中STR基因座的突变特征和规律。 [方法]收集了2017年至2020年从海南省县和城市获得的法医医学识别中心接受的2715名父级测试用例,选择了含基因突变的病例,突变率和每个细节计算基因座,分析了23 str基因座的突变调节率。 [结果] 2715例鉴定为“支持”,1487例是三重态病例,1640例是Dyad病例,总计4614 Meiose;存在50个基因突变事件(包括17个三重型突变和33个Dyad突变),平均突变率为0.0047%,累积突变率为1.0837%。 23 str基因座中总共19个突变,突变率在D12S391基因座中为0.1301%,50.0217%在五个基因座,TPOX,D1S1656,D2S441,D22S1045和五边构,而没有发现异标事件四个LOCI,D19S433,TH01,D13S317和D7S820。在50个突变事件中,47例是一步突变,1是两步,2分三步。父亲突变(13个三联和22个二元),6个母体突变(4个三体和2个二元),和9个不确定的患者蛋白/母体突变,父母突变比为5.83:1。 [结论] D12S391基因座的突变率最高,TPOX,D1S1656,D2S441,D22S1045和PENTAD LOCI的突变率是海南人群中最低的,并且父突变突变大于母体突变。在父权测试中,如果1 - 3 str基因座不符合遗传法,特别是当突变轨迹是纯合的或亲属的下一个识别时,则必须使用其他套件来审查和增加数量基因座或使用第二代排序技术确认,小心地解除突变并确保识别结论的准确性。

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