Institute of Forensic Medicine, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu 610041, China.
Institute of Forensic Medicine, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu 610041, China.
Forensic Sci Int Genet. 2019 Sep;42:171-180. doi: 10.1016/j.fsigen.2019.07.015. Epub 2019 Jul 25.
During the last decade, RNA profiling has emerged as one of the fastest developed methods for discriminating forensically relevant biological samples. As a category of small non-coding RNA, piwi-interacting RNA (piRNA) has recently been proposed to be differentially expressed in different types of body fluids, which indicates that its potential in forensic science is worth exploring. In this study, small RNA from 6 types of biological samples (venous blood, menstrual blood, saliva, semen, vaginal secretions and skin) was prepared and sequenced in order to characterize the expression pattern of piRNA using Ion S5 XL platform. Multiple bioinformatic methods were applied to make interpretation of the massively parallel sequencing data and identify representative biomarkers. A total of 376 piRNAs were initially identified after normalization and filtering. Hierarchical clustering and partial least squares-discriminant analysis (PLS-DA) revealed that their expression profiles exhibited an acceptable discriminating ability for most biological samples. Besides, a panel consists of 37 piRNA candidates was subsequently established for further analysis. The results suggested that with the optimal number of PLS components, the marker-reduced panel was sufficient to construct a PLS-DA model with the same performance as that can be achieved by the entire 376 piRNAs (classification error rate = 0.04). In addition, 5 targeted candidates were further selected for validation. TaqMan RT-qPCR assay results verified the potential of 3 piRNAs (piR-hsa-27622, piR-hsa-1207 and piR-hsa-27493) in distinguishing venous blood and menstrual blood, as well as 2 piRNA (piR-hsa-27493 and piR-hsa-26591) for the discrimination of saliva and vaginal secretions, which emphasized the feasibility of our biomarker selection approach. In brief, our study expanded the amount of potential piRNA biomarkers and demonstrated that the expression features of piRNA could provide valuable information for discriminating forensically relevant biological samples.
在过去的十年中,RNA 分析已成为鉴别法医学相关生物样本的发展最快的方法之一。piRNA 是小非编码 RNA 的一种,最近有研究提出它在不同类型的体液中有差异表达,这表明它在法医学中的应用潜力值得探索。在本研究中,我们从 6 种生物样本(静脉血、月经血、唾液、精液、阴道分泌物和皮肤)中提取小 RNA,使用 Ion S5XL 平台测序,以特征化 piRNA 的表达模式。应用多种生物信息学方法对大规模平行测序数据进行解释和鉴定有代表性的生物标志物。经过归一化和过滤后,初步鉴定出 376 个 piRNA。层次聚类和偏最小二乘判别分析(PLS-DA)显示,它们的表达谱对大多数生物样本具有可接受的区分能力。此外,随后建立了一个由 37 个 piRNA 候选物组成的面板进行进一步分析。结果表明,通过最佳数量的 PLS 成分,标记减少的面板足以构建与使用整个 376 个 piRNA (分类错误率 = 0.04)相同性能的 PLS-DA 模型。此外,进一步选择了 5 个靶向候选物进行验证。TaqMan RT-qPCR 检测结果验证了 3 个 piRNA(piR-hsa-27622、piR-hsa-1207 和 piR-hsa-27493)在区分静脉血和月经血中的潜力,以及 2 个 piRNA(piR-hsa-27493 和 piR-hsa-26591)在区分唾液和阴道分泌物中的潜力,这强调了我们的生物标志物选择方法的可行性。总之,本研究扩展了潜在 piRNA 生物标志物的数量,并证明了 piRNA 的表达特征可为鉴别法医学相关生物样本提供有价值的信息。