Forat Sophia, Huettel Bruno, Reinhardt Richard, Fimmers Rolf, Haidl Gerhard, Denschlag Dominik, Olek Klaus
Labor für Abstammungsbegutachtungen GmbH, Rheinbach, Germany.
Max Planck Genome Centre Cologne Institute for Breeding Research, Cologne, Germany.
PLoS One. 2016 Feb 1;11(2):e0147973. doi: 10.1371/journal.pone.0147973. eCollection 2016.
The identification of body fluids is an essential tool for clarifying the course of events at a criminal site. The analytical problem is the fact that the biological material has been very often exposed to detrimental exogenous influences. Thereby, the molecular substrates used for the identification of the traces may become degraded. So far, most protocols utilize cell specific proteins or RNAs. Instead of measuring these more sensitive compounds this paper describes the application of the differential DNA-methylation. As a result of two genome wide screenings with the Illumina HumanMethylation BeadChips 27 and 450k we identified 150 candidate loci revealing differential methylation with regard to the body fluids venous blood, menstrual blood, vaginal fluid, saliva and sperm. Among them we selected 9 loci as the most promising markers. For the final determination of the methylation degree we applied the SNuPE-method. Because the degree of methylation might be modified by various endogenous and exogenous factors, we tested each marker with approximately 100 samples of each target fluid in a validation study. The stability of the detection procedure is proved in various simulated forensic surroundings according to standardized conditions. We studied the potential influence of 12 relatively common tumors on the methylation of the 9 markers. For this purpose the target fluids of 34 patients have been analysed. Only the cervix carcinoma might have an remarkable effect because impairing the signal of both vaginal markers. Using the Illumina MiSeq device we tested the potential influence of cis acting sequence variants on the methylation degree of the 9 markers in the specific body fluid DNA of 50 individuals. For 4 marker loci we observed such an influence either by sole SNPs or haplotypes. The identification of each target fluid is possible in arbitrary mixtures with the remaining four body fluids. The sensitivity of the individual body fluid tests is in the same range as for the forensic STR-analysis. It is the first forensic body fluid protocol which considers the exogenic and endogenic parameters potentially interfering with the true results.
体液鉴定是厘清犯罪现场事件过程的一项重要工具。分析难题在于生物材料经常受到有害的外部影响。因此,用于痕迹鉴定的分子底物可能会降解。到目前为止,大多数方案都利用细胞特异性蛋白质或RNA。本文描述的不是测量这些更敏感的化合物,而是应用差异DNA甲基化。通过使用Illumina HumanMethylation BeadChips 27和450k进行的两次全基因组筛选,我们确定了150个候选基因座,这些基因座在静脉血、经血、阴道液、唾液和精液等体液中显示出差异甲基化。其中,我们选择了9个基因座作为最有前景的标记。为了最终确定甲基化程度,我们应用了单核苷酸引物延伸法(SNuPE法)。由于甲基化程度可能会受到各种内源性和外源性因素的影响,我们在一项验证研究中用每种目标体液的约100个样本对每个标记进行了测试。根据标准化条件,在各种模拟法医环境中证明了检测程序的稳定性。我们研究了12种相对常见的肿瘤对9个标记甲基化的潜在影响。为此,分析了34名患者的目标体液。只有宫颈癌可能有显著影响,因为它会削弱两种阴道标记的信号。我们使用Illumina MiSeq设备测试了顺式作用序列变异对50个人特定体液DNA中9个标记甲基化程度的潜在影响。对于4个标记基因座,我们观察到单独的单核苷酸多态性(SNP)或单倍型会产生这种影响。在与其他四种体液的任意混合物中都可以鉴定出每种目标体液。个体体液检测的灵敏度与法医短串联重复序列(STR)分析的灵敏度在同一范围内。这是第一个考虑到可能干扰真实结果的外源性和内源性参数的法医体液鉴定方案。