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中国汉族人群中 28 个常染色体短串联重复序列的突变分析。

Mutation analysis of 28 autosomal short tandem repeats in the Chinese Han population.

机构信息

Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Mol Biol Rep. 2021 Jun;48(6):5363-5369. doi: 10.1007/s11033-021-06522-7. Epub 2021 Jul 2.

DOI:10.1007/s11033-021-06522-7
PMID:34213710
Abstract

Short tandem repeats (STRs) have been extensively used in forensic genetics. However, according to previous studies, the mutation rates of STRs are relatively high and are affected by many factors. Therefore, it is important to analyze STR mutations and determine the influence of underlying factors on STR mutation rates. Mutation rates of 28 autosomal STRs were determined from 8708 paternity testing cases in the Chinese Han population, and the relationships between STR mutation rates and population, sex, age, allele length and heterozygosity were investigated. A total of 279 mutations were observed at 27 loci in a total of 233,530 meiosis cases, including 273 (97.8%) one-step, 5 (1.8%) two-step and 1 (0.4%) three-step mutations. The overall average mutation rate was 1.19 × 10 (95% CI 1.06 × 10 - 1.34 × 10) ranging from 0 (TPOX) to 2.79 × 10 (D13S325). Mutation rate comparisons revealed statistically significant differences at several STRs among populations. Paternal mutations occurred more frequently than maternal mutations, at a ratio of 6.04:1, and the mutation rate tended to increase with paternal age. Moreover, our study revealed a bias towards contraction mutations for long alleles and expansion mutations for short alleles. No obvious bias was observed in the overall mutation direction. In addition, STR loci with higher expected heterozygosity (H) tended to have higher mutation rates. This work revealed the relationships between STR mutation rates and several influencing factors, providing useful data and information for further research on STR mutations in forensic genetics.

摘要

短串联重复序列(STRs)在法医遗传学中得到了广泛应用。然而,根据以往的研究,STR 的突变率相对较高,并且受到许多因素的影响。因此,分析 STR 突变并确定潜在因素对 STR 突变率的影响非常重要。本研究从中国汉族人群的 8708 例亲子鉴定案例中确定了 28 个常染色体 STR 的突变率,并调查了 STR 突变率与人群、性别、年龄、等位基因长度和杂合度的关系。在总共 233530 次减数分裂中,在 27 个位点观察到了 279 个突变,包括 273 个(97.8%)一步突变、5 个(1.8%)二步突变和 1 个(0.4%)三步突变。总的平均突变率为 1.19×10(95%置信区间为 1.06×10-1.34×10),范围从 0(TPOX)到 2.79×10(D13S325)。突变率比较显示,不同人群之间的几个 STR 存在统计学差异。父系突变比母系突变更频繁,比例为 6.04:1,并且突变率随着父系年龄的增加而增加。此外,我们的研究还揭示了长等位基因偏向收缩突变,短等位基因偏向扩张突变的趋势。总体突变方向没有明显的偏差。此外,预期杂合度(H)较高的 STR 位点倾向于具有较高的突变率。本研究揭示了 STR 突变率与几个影响因素之间的关系,为法医遗传学中 STR 突变的进一步研究提供了有用的数据和信息。

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本文引用的文献

1
[Mutation Analysis of 19 STR Loci in 20 723 Cases of Paternity Testing].20723例亲子鉴定中19个STR基因座的突变分析
Fa Yi Xue Za Zhi. 2017 Jun;33(3):263-266. doi: 10.3969/j.issn.1004-5619.2017.03.010. Epub 2017 Jun 25.
2
Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material.Chelex 100作为一种从法医材料中简单提取用于基于PCR分型的DNA的介质。
Biotechniques. 1991 Apr;10(4):506-13.