Differentiation of five forensically relevant body fluids using a small set of microRNA markers

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Linus Altmeyer, Karine Baumer, Diana Hall
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Abstract

In forensic investigations, identifying the type of body fluid allows for the interpretation of biological evidence at the activity level. Over the past two decades, significant research efforts have focused on developing molecular methods for this purpose. MicroRNAs (miRNAs) hold great promise due to their tissue-specific expression, abundance, lack of splice variants, and relative stability. Although initial findings are promising, achieving consistent results across studies is still challenging, underscoring the necessity for both original and replication studies. To address this, we selected 18 miRNA candidates and tested them on 6 body fluids commonly encountered in forensic cases: peripheral blood, menstrual blood, saliva, semen, vaginal secretion, and skin. Using reverse transcription quantitative PCR analysis, we confirmed eight miRNA candidates (miR-144-3p, miR-451a, miR-205-5p, miR-214-3p, miR-888-5p, miR-891a-5p, miR-193b-3p, miR-1260b) with high tissue specificity and four (miR-203a-3p, miR-141-3p, miR-200b-3p, miR-4286) with lesser discrimination ability but still contributing to body fluid differentiation. Through principal component analysis and hierarchical clustering, the set of 12 miRNAs successfully distinguished all body fluids, including the challenging discrimination of blood from menstrual blood and saliva from vaginal secretion. In conclusion, our results provide additional data supporting the use of a small set of miRNAs for predicting common body fluids in forensic contexts. Large population data need to be gathered to develop a body fluid prediction model and assess its accuracy.

Abstract Image

利用一小套 microRNA 标记区分五种与法医相关的体液。
在法医调查中,确定体液的类型有助于从活动层面解读生物证据。在过去二十年中,大量研究工作集中在为此开发分子方法上。微小核糖核酸(miRNA)因其组织特异性表达、丰度、缺乏剪接变体和相对稳定性而大有可为。虽然初步研究结果很有希望,但要在不同研究中取得一致的结果仍然具有挑战性,这就强调了原始研究和重复研究的必要性。为了解决这个问题,我们选择了 18 种候选 miRNA,并在法医案件中常见的 6 种体液(外周血、经血、唾液、精液、阴道分泌物和皮肤)上进行了测试。通过反转录定量 PCR 分析,我们确认了 8 个候选 miRNA(miR-144-3p、miR-451a、miR-205-5p、miR-214-3p、miR-888-5p、miR-891a-5p、miR-193b-3p、miR-1260b)具有较高的组织特异性,4 个候选 miRNA(miR-203a-3p、miR-141-3p、miR-200b-3p、miR-4286)的鉴别能力较弱,但仍有助于体液分化。通过主成分分析和分层聚类,12 个 miRNA 成功区分了所有体液,包括具有挑战性的血液与经血、唾液与阴道分泌物的区分。总之,我们的研究结果提供了更多数据,支持使用一小组 miRNA 预测法医环境中的常见体液。要开发体液预测模型并评估其准确性,还需要收集大量的人群数据。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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