College of Forensic Science, Xi'an Jiaotong University Health Science Center, Xi'an, China; Medical Genetic Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, China; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Key Laboratory of Population Defects Prevention, Zhengzhou, China.
Medical Genetic Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, China.
Forensic Sci Int. 2023 Dec;353:111848. doi: 10.1016/j.forsciint.2023.111848. Epub 2023 Sep 26.
Microhaplotypes (MHs), small sets of linked single nucleotide polymorphisms (SNPs), are becoming a valuable tool for paternity testing, personal identification and other different forensic purposes due to their advantages of both short tandem repeats (STRs) and SNPs. However, only a small part of MHs with small segments have been developed and reported so far. And the current population genetic data of MHs are still insufficient. MHs with small segments possess unique advantages in mixture deconvolution, degradation material identification, noninvasive prenatal paternity testing and even medical tumor diagnostic applications. In the present study, a set of 90 autosomal MHs whose PCR amplicon lengths are from 90-150 bp, of which 58 MHs are less than or equal to 100 bp are selected, and assembled into an amplification multiplex system optimized for Ion S5™ System for forensic application. Genetic diversity study of 90 MHs in the populations from different intercontinental regions shows that the polymorphism information content (PIC) values of 83 MHs are greater than 0.4 in populations from East Asia (EAS), and the average PIC value of 90 MHs is greater than 0.5. A total of EAS populations shows the highest cumulative match probability (CMP) and cumulative probability of exclusion (CPE) values in five intercontinental populations. The CMP and CPE values of 90 MHs in EAS are 1.1688 × 10 and 0.999999999998954. The informativeness for assignment (In) values of the 90 MHs are calculated based on data from five intercontinental populations, and the In values of 20 MHs have greater than 0.1, indicating that the 20 MHs are high effectiveness in distinguishing different intercontinental populations, which can be used as candidate ancestry informative markers. Further, we have studied the polymorphisms of the 90 MHs based on 224 unrelated individuals of Henan Han population, China, and obtained the frequency data of the 90 MHs. In the Henan Han population, the effective number of alleles (Ae) of the 90 MHs ranges from 1.7649 (MH45) to 3.9792 (MH50), and the Ae values of 10 MHs reach to 3.0; the Ae values of 80 MHs are greater than 2, and the average Ae value for these MHs is 2.422. The average expected heterozygosity, observed heterozygosity, PIC, matching probability, discrimination power and probability of exclusion values of 90 MHs in the Henan Han population are 0.5788, 0.5851, 0.5039, 0.2608, 0.7392 and 0.2806, respectively. The CMP value of 90 MHs in the study population is less than 10, and their CPE value reaches 0.999999999999999923. Moreover, the results of the depth of coverage, allele coverage ratio and noise level indicate that the 90 MH amplification system has well sequencing performance, and the sequencing results are reliable. The results indicate the 90 MHs show higher polymorphisms in the study population. The present panel can be well used in paternity testing and individual identification in the study population and even the populations from EAS.
微单倍型(MHs)是短串联重复序列(STRs)和单核苷酸多态性(SNPs)的优势组合,是一种新的遗传标记物,目前已经在亲子鉴定、个人识别和其他不同的法医应用中得到了广泛的应用。本研究中,我们选择了 90 个常染色体 MHs,其 PCR 扩增片段长度为 90-150bp,其中 58 个 MHs小于或等于 100bp,将其组装成一个优化的扩增多重体系,适用于 Ion S5™系统的法医应用。来自不同洲际人群的 90 个 MHs的遗传多样性研究表明,东亚(EAS)人群中 83 个 MHs的多态信息含量(PIC)值大于 0.4,90 个 MHs的平均 PIC 值大于 0.5。在五个洲际人群中,EAS 人群的累积匹配概率(CMP)和累积排除概率(CPE)值最高。EAS 人群中 90 个 MHs 的 CMP 和 CPE 值分别为 1.1688×10-16 和 0.999999999998954。基于五个洲际人群的数据,计算了 90 个 MHs的信息量赋值(In)值,其中 20 个 MHs的 In 值大于 0.1,表明这 20 个 MHs在区分不同洲际人群方面具有较高的有效性,可作为候选的遗传来源信息标记物。此外,我们还对来自中国河南汉族的 224 名无关个体的 90 个 MHs进行了多态性研究,获得了 90 个 MHs的频率数据。在河南汉族人群中,90 个 MHs的有效等位基因数(Ae)范围为 1.7649(MH45)至 3.9792(MH50),10 个 MHs的 Ae 值达到 3.0;80 个 MHs的 Ae 值大于 2,这些 MHs的平均 Ae 值为 2.422。河南汉族人群中 90 个 MHs的平均预期杂合度、观察杂合度、PIC、匹配概率、鉴别能力和排除概率值分别为 0.5788、0.5851、0.5039、0.2608、0.7392 和 0.2806。90 个 MHs在研究人群中的 CMP 值小于 10,其 CPE 值达到 0.999999999999999923。此外,深度覆盖率、等位基因覆盖率和噪声水平的结果表明,90 个 MH 扩增系统具有良好的测序性能,测序结果可靠。研究结果表明,90 个 MHs在研究人群中表现出较高的多态性。本panel 可用于研究人群以及东亚人群的亲子鉴定和个体识别。