Construction of A Novel 5-Dye Fluorescent Multiplex System With 30 Y-STRs for Patrilineal Relationship Prediction.

IF 2.5 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-08-20 DOI:10.1002/elps.70015
Chaoran Sun, Zhirui Zhang, Xindi Wang, Bo Liu, Chengye Zhou, Yufei Yang, Chuanxu Wang, Sunxi Xu, Chang Wang, Lagabaiyila Zha, Jienan Li, Haibo Luo, Feng Song
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Abstract

Nowadays, Y chromosome short tandem repeats (Y-STRs) are widely used in forensic medicine practice, which has great significance for ancestry tracing, male lineage evolution, and male paternal relatives. Rapidly mutating Y-STRs (RM Y-STRs) have been shown to have greater potential to distinguish males from males in the patrilineal line. Therefore, a novel 5-dye fluorescent multiplex system with 30 Y-STRs was developed and optimized to screen out more RM Y-STRs and fasting mutating Y-STRs (FM Y-STRs). New primers were designed, and composite system construction was carried out. A series of experiments were conducted following the guidelines of the Scientific Working Group on DNA Analysis Methods (SWGDAM), including polymerase chain reaction (PCR) amplification conditions, sensitivity, stability, species specificity, mixture and degraded sample studies, mutation analysis, and population studies. The results suggested that changing PCR amplification conditions in a reasonable range hardly affected the genotyping. The system showed excellent sensitivity and stability in sensitivity and stability studies. Even with UV-C exposure for up to 96 h, the system performed well in male blood samples and semen-vaginal secretion mixtures. Mutation analysis was performed on 582 father-son pairs, and 4 RM Y-STRs and 7 FM Y-STRs were identified, with mutation rates ranging from 1.72 × 10-3 to 20.62 × 10-3. Furthermore, on the basis of mutation rate analysis, eight machine learning methods were used to construct and compare patrilineal relationship prediction models, inferring the relationship by predicting the number of meiosis. Overall, the multiplex system displays favorable performance and has a greater potential for application in forensic science practice.

30个Y-STRs的新型5染料荧光多路系统的构建用于父系关系预测。
目前,Y染色体短串联重复序列(Y- strs)在法医学实践中得到了广泛的应用,对祖先溯源、男性谱系进化、男性父系亲缘关系研究具有重要意义。快速突变的Y-STRs (RM Y-STRs)在父系系中具有更大的区分雄性的潜力。因此,我们开发并优化了一种含有30个Y-STRs的新型5染料荧光多路系统,以筛选更多的RM Y-STRs和禁食突变Y-STRs (FM Y-STRs)。设计了新型底漆,并进行了复合体系的构建。按照DNA分析方法科学工作组(SWGDAM)的指导方针进行了一系列实验,包括聚合酶链反应(PCR)扩增条件、敏感性、稳定性、物种特异性、混合和降解样品研究、突变分析和群体研究。结果表明,在合理范围内改变PCR扩增条件对基因分型影响不大。该系统在灵敏度和稳定性研究中表现出良好的灵敏度和稳定性。即使暴露于UV-C长达96小时,该系统在男性血液样本和精液-阴道分泌物混合物中也表现良好。对582对父子进行突变分析,鉴定出4对RM Y-STRs和7对FM Y-STRs,突变率在1.72 × 10-3 ~ 20.62 × 10-3之间。在突变率分析的基础上,采用8种机器学习方法构建父系关系预测模型并进行比较,通过预测减数分裂数来推断父系关系。综上所述,该系统表现出良好的性能,在法医学实践中具有较大的应用潜力。
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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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