School of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, 453003, People's Republic of China.
School of Basic Medicine, Sanquan College of Xinxiang Medical University, Xinxiang, Henan, 453003, People's Republic of China.
Int J Legal Med. 2023 Sep;137(5):1413-1419. doi: 10.1007/s00414-023-03044-8. Epub 2023 Jul 6.
In the practice of parentage testing, short tandem repeat (STR) genetic inconsistencies occasionally occur and are usually treated as genetic mutations. However, they arise for various reasons. To elucidate the reasons for their occurrence, this study investigates a typical trio. For the D6S1043 locus, the genotype of the biological mother comprised the heterozygous alleles "7,20"; that of the child, allele 20; and that of the alleged father, a heterozygous allele "11,13," revealing a 7-step mutation. Different kits were first used to verify the data. The locus map, primers, and core sequences were then analyzed. Ultimately, the STR and single nucleotide polymorphisms of 6q were tested to determine the microdeletion range. The results revealed that this was indeed a true trio, and the underlying cause of the genetic inconsistency at this locus was a microdeletion of approximately 0.74-1.78 Mb in 6q15. Overall, genetic inconsistencies detected during practical work, and particularly rare multi-step mutations, cannot be directly identified as STR mutations. Different tools should be used to examine the causes of genetic inconsistencies from various perspectives and improve the effectiveness of genetic evidence.
在亲权鉴定实践中,短串联重复(STR)遗传不一致偶尔会发生,通常被视为基因突变。然而,它们的发生有多种原因。为了阐明其发生的原因,本研究调查了一个典型的三联体。对于 D6S1043 基因座,生物母亲的基因型由杂合子等位基因“7,20”组成;孩子的基因型为等位基因 20;假定父亲的基因型为杂合子等位基因“11,13”,显示出 7 步突变。首先使用不同的试剂盒来验证数据。然后分析了基因座图谱、引物和核心序列。最后,测试了 6q 的 STR 和单核苷酸多态性,以确定微缺失范围。结果表明,这确实是一个真正的三联体,该基因座遗传不一致的根本原因是 6q15 中约 0.74-1.78 Mb 的微缺失。总的来说,在实际工作中检测到的遗传不一致,特别是罕见的多步突变,不能直接被认定为 STR 突变。应该使用不同的工具从不同角度检查遗传不一致的原因,提高遗传证据的有效性。