Cho Mun-Jeong, Park Seung-Jin, Lee Hwan Young, Park Jong-Lyul, Lee Seung Mi, Kim Jae-Yoon, Lee So-Yeon, Kim Seon-Young, Jun Jong Kwan, Lee Soong Deok
Department of Functional Genomics, University of Science and Technology, Daejeon 34141, Republic of Korea.
Personalized Genomic Medicine Research Center, KRIBB, Daejeon 34141, Republic of Korea.
Forensic Sci Int Genet. 2025 Sep;79:103307. doi: 10.1016/j.fsigen.2025.103307. Epub 2025 May 28.
In the current forensic environment, short tandem repeat (STR) profiling originating from genomic differences is highly accurate and widely used to identify individuals. However, if the person of interest is a monozygotic (MZ) twin, his or her DNA profile is identical to that of his or her twin; thus, STR profiling cannot discriminate between them. Therefore, DNA methylation, which is known to have different patterns even in MZ twins, has attracted attention as a promising marker to differentiate MZ twins. These epigenetic patterns are affected by environmental factors and age, and distinct DNA methylation patterns have been observed among the three types of MZ twins, i.e., dichorionic-diamniotic, monochorionic-diamniotic, and monochorionic-monoamniotic. To compare DNA methylation profiles among these three types of MZ twins and identify common markers to differentiate MZ twins, we collected cord blood samples from 54 pairs of MZ twins and analyzed their DNA methylation profiles using the Human MethylationEPIC v2.0 platform. The differences in DNA methylation observed among the three types of MZ twins occurred in immune-related regions. Differentially methylated genes identified in both monochorionic-diamniotic and monochorionic-monoamniotic twins were enriched in cytokine signaling and interleukin signaling-related regions. However, differentially methylated genes in dichorionic-diamniotic twins were enriched in PPI at synapse and the neuronal system. To facilitate twin differentiation, we selected a combination of CpG sites that differed between MZ twins and validated this CpG combination in two independent cohorts comprising 118 British MZ twin pairs and 47 Korean MZ twin pairs. Additionally, these selected DNA methylation markers were evaluated in 60 independent samples of MZ twins using pyrosequencing. Our results suggest that the methylation differences observed between MZ twins at birth persist throughout life. Consequently, these CpG site combinations could serve as valuable methylation markers in forensic cases where a suspect is a MZ twin.
在当前的法医环境中,源自基因组差异的短串联重复序列(STR)分析高度准确,被广泛用于识别个体。然而,如果感兴趣的人是同卵(MZ)双胞胎,其DNA图谱与他或她的双胞胎相同;因此,STR分析无法区分他们。因此,即使在MZ双胞胎中也具有不同模式的DNA甲基化,作为区分MZ双胞胎的有前景的标记物受到了关注。这些表观遗传模式受环境因素和年龄影响,并且在三种类型的MZ双胞胎中观察到了不同的DNA甲基化模式,即双绒毛膜双羊膜囊、单绒毛膜双羊膜囊和单绒毛膜单羊膜囊。为了比较这三种类型的MZ双胞胎之间的DNA甲基化图谱并识别区分MZ双胞胎的共同标记物,我们收集了54对MZ双胞胎的脐带血样本,并使用人类甲基化EPIC v2.0平台分析了他们的DNA甲基化图谱。在这三种类型的MZ双胞胎中观察到的DNA甲基化差异发生在免疫相关区域。在单绒毛膜双羊膜囊和单绒毛膜单羊膜囊双胞胎中鉴定出的差异甲基化基因在细胞因子信号传导和白细胞介素信号传导相关区域富集。然而,双绒毛膜双羊膜囊双胞胎中的差异甲基化基因在突触和神经系统的蛋白质-蛋白质相互作用(PPI)中富集。为了便于双胞胎区分,我们选择了MZ双胞胎之间不同的CpG位点组合,并在由118对英国MZ双胞胎和47对韩国MZ双胞胎组成的两个独立队列中验证了这种CpG组合。此外,使用焦磷酸测序在60个MZ双胞胎的独立样本中评估了这些选定的DNA甲基化标记物。我们的结果表明,MZ双胞胎出生时观察到的甲基化差异终生持续存在。因此,这些CpG位点组合可以作为法医案件中嫌疑人是MZ双胞胎时的有价值的甲基化标记物。