Department of Forensic Genetics, West China School of Basic Science and Forensic Medicine, Sichuan University (West China University of Medical Sciences), Chengdu 610041, Sichuan, China.
Forensic Sci Int Genet. 2012 May;6(3):419-23. doi: 10.1016/j.fsigen.2011.08.008. Epub 2011 Sep 7.
MicroRNAs (miRNAs, 18-25 bases in length) are small, non-coding RNAs that regulate gene expression at the post-transcriptional level. MiRNA expression patterns, including presence and relative abundance of particular miRNA species, provide cell- and tissue-specific information that can be used for body fluid identification. Recently, two published studies reported that a number of body fluid-specific miRNAs had been identified. However, the results were inconsistent when different technology platforms and statistical methods were applied. To further study the role of miRNAs in identification of body fluids, this study sets out to develop an accurate and reliable model for data analysis of miRNA expression. To that end, the relative expression levels of three miRNAs were studied using the mirVana™ miRNA Isolation Kit, high-specificity stem-loop reverse transcription (RT) and high-sensitivity hydrolysis probes (TaqMan) quantitative real-time polymerase chain reaction (qPCR) in forensically relevant biological fluids, including venous blood, vaginal secretions, menstrual blood, semen and saliva. Accurate quantification of miRNAs requires not only a highly sensitive and specific detection platform for experiment operation, but also a reproducible methodology with an adequate model for data analysis. In our study, the efficiency-calibrated model that incorporated the impact of the quantification cycle (Cq) values and PCR efficiencies of target and reference genes was developed to calculate the relative expression ratio of miRNAs in forensically relevant body fluids. Our results showed that venous blood was distinguished from other body fluids according to the relative expression ratio of miR16 using as little as 50pg of total RNA, while the expression level of miR658 was unstable and that of miR205 was nonspecific among different body fluids. Collectively, the findings may constitute a basis for future miRNA-based research on body fluid identification and show miRNAs as a promising biomarker in forensic identification of body fluids.
微小 RNA(miRNA,18-25 个碱基长)是一种小的非编码 RNA,可在转录后水平调节基因表达。miRNA 的表达模式,包括特定 miRNA 种类的存在和相对丰度,提供了可用于体液鉴定的细胞和组织特异性信息。最近,有两项已发表的研究报告称,已经鉴定出了一些具有体液特异性的 miRNA。然而,当应用不同的技术平台和统计方法时,结果并不一致。为了进一步研究 miRNA 在体液鉴定中的作用,本研究旨在开发一种用于 miRNA 表达数据分析的准确可靠的模型。为此,本研究使用 mirVana™ miRNA 分离试剂盒、高特异性茎环反转录(RT)和高灵敏度水解探针(TaqMan)定量实时聚合酶链反应(qPCR)研究了三种 miRNA 在法医相关生物体液中的相对表达水平,包括静脉血、阴道分泌物、月经血、精液和唾液。miRNA 的准确定量不仅需要实验操作具有高度灵敏和特异的检测平台,还需要具有可重复的方法学和用于数据分析的充分模型。在本研究中,开发了一种效率校准模型,该模型纳入了定量循环(Cq)值和靶基因和参考基因的 PCR 效率的影响,用于计算法医相关体液中 miRNA 的相对表达比率。我们的结果表明,使用 50pg 总 RNA 即可根据 miR16 的相对表达比率将静脉血与其他体液区分开来,而 miR658 的表达水平在不同体液中不稳定,miR205 的表达水平无特异性。总之,这些发现可能为未来基于 miRNA 的体液鉴定研究奠定基础,并表明 miRNA 作为法医鉴定体液的一种有前途的生物标志物。