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用于检测不平衡降解DNA混合物和无创产前亲子鉴定的15个单核苷酸多态性-单核苷酸多态性标记组

Set of 15 SNP-SNP Markers for Detection of Unbalanced Degraded DNA Mixtures and Noninvasive Prenatal Paternity Testing.

作者信息

Zhang Ranran, Tan Yu, Wang Li, Jian Hui, Zhu Jing, Xiao Yuanyuan, Tan Mengyu, Xue Jiaming, Yang Fan, Liang Weibo

机构信息

Department of Forensic Genetics, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, China.

Department of Obstetrics and Gynecology, West China Second University Hospital, Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, Sichuan University, Chengdu, China.

出版信息

Front Genet. 2022 Feb 10;12:800598. doi: 10.3389/fgene.2021.800598. eCollection 2021.

Abstract

Unbalanced and degraded mixtures (UDM) are very common in forensic DNA analysis. For example, DNA signals from criminal suspects are masked by a large amount of DNA from victims, or cell-free fetal DNA (cffDNA) in maternal plasma is masked by a high background of maternal DNA. Currently, detecting minor DNA in these mixtures is complex and challenging. We developed a new set of SNP-SNP microhaplotypes with short amplicons, and we successfully genotyped them using the new method of amplification-refractory mutation system PCR (ARMS-PCR) combined with SNaPshot technology based on a capillary electrophoresis (CE) platform. This panel reflects a high polymorphism in the Southwest Chinese Han population and thus has excellent potential for mixture studies. We evaluated the feasibility of this panel for UDM detection and noninvasive prenatal paternity testing (NIPPT). Fifteen SNP-SNPs detected minor DNA of homemade DNA mixtures, with a sensitivity of 0.025-0.05 ng and a specificity of 1:1,000. In addition, the panel successfully genotyped degraded DNA from single and mixed samples. Finally, 15 SNP-SNPs were applied to 26 trios. All samples displayed positive results with at least one marker to detect cffDNA. Besides, all fetal alleles in maternal plasma were confirmed by genotyping fetal genomic DNA from amniocentesis and paternal genomic DNA from peripheral blood. The results indicated that the SNP-SNP strategy based on the CE platform was useful for UDM detection and NIPPT.

摘要

不平衡和降解的混合物(UDM)在法医DNA分析中非常常见。例如,犯罪嫌疑人的DNA信号被来自受害者的大量DNA掩盖,或者母血浆中的游离胎儿DNA(cffDNA)被高背景的母体DNA掩盖。目前,在这些混合物中检测微量DNA既复杂又具有挑战性。我们开发了一组新的具有短扩增子的SNP-SNP微单倍型,并使用基于毛细管电泳(CE)平台的扩增不应突变系统PCR(ARMS-PCR)结合SNaPshot技术的新方法成功对其进行了基因分型。该面板在中国西南汉族人群中反映出高度多态性,因此在混合物研究方面具有出色的潜力。我们评估了该面板用于UDM检测和无创产前亲子鉴定(NIPPT)的可行性。15个SNP-SNP检测到自制DNA混合物中的微量DNA,灵敏度为0.025-0.05 ng,特异性为1:1000。此外,该面板成功对来自单一和混合样本的降解DNA进行了基因分型。最后,将15个SNP-SNP应用于26个三联体。所有样本至少有一个标记显示阳性结果以检测cffDNA。此外,通过对羊膜穿刺术获得的胎儿基因组DNA和外周血获得的父体基因组DNA进行基因分型,确认了母血浆中的所有胎儿等位基因。结果表明,基于CE平台的SNP-SNP策略可用于UDM检测和NIPPT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c93/8866868/4cadadc88c85/fgene-12-800598-g001.jpg

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