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Development of a novel panel for blood identification based on blood-specific CpG-linked SNP markers.
Li, Zeqin; Liu, Na; Yuan, Fang; Guan, Zimeng; Liu, Jinding; Liu, Feng; Ren, Jianbo; Yan, Jiangwei; Zhang, Gengqian.
Afiliación
  • Li Z; School of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
  • Liu N; Shanxi Key Laboratory of Forensic Medicine, Jinzhong, 030600, Shanxi, China.
  • Yuan F; School of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
  • Guan Z; Shanxi Key Laboratory of Forensic Medicine, Jinzhong, 030600, Shanxi, China.
  • Liu J; School of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
  • Liu F; Shanxi Key Laboratory of Forensic Medicine, Jinzhong, 030600, Shanxi, China.
  • Ren J; Department of Biotechnology, Biomedical Sciences College, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, 250117, Shandong, China.
  • Yan J; School of Forensic Medicine, Shanxi Medical University, Jinzhong, 030600, Shanxi, China.
  • Zhang G; Shanxi Key Laboratory of Forensic Medicine, Jinzhong, 030600, Shanxi, China.
Int J Legal Med ; 138(3): 1205-1219, 2024 May.
Article en En | MEDLINE | ID: mdl-37853302
ABSTRACT
Blood-containing mixtures often appear in murder and robbery cases, and their identification plays a significant role in solving crimes. In recent years, the co-detection of DNA methylation markers (CpG) and single nucleotide polymorphism (SNP) markers has been shown to be a promising tool for the identification of semen and its donor. However, similar research on blood stains that are frequently found at crime scenes has not yet been reported. In this study, we employed blood-specific CpG-linked SNP markers (CpG-SNP) for blood-specific genotyping and the linking of blood and its donor. The tissue-specific CpG markers were screened from the literature and further verified by combining bisulfite conversion with amplification-refractory mutation system (ARMS) technology. Meanwhile, adjacent SNP markers with a minor allele frequency (MAF) greater than 0.1 were selected within 400 bp upstream and downstream of the CpG markers. SNP genotyping was performed using SNaPshot technology on a capillary electrophoresis (CE) platform. Finally, a multiplex panel, including 19 blood-specific CpG linked to 23 SNP markers, as well as 1 semen-specific CpG, 1 vaginal secretion-specific CpG, and 1 saliva-specific CpG marker, was constructed successfully. The panel showed good tissue specificity and blood stains stored at room temperature for up to nine months and moderately degraded (4 < DI < 10) could be effectively identified. Moreover, it could also be detected when blood content in the mixed stains was as low as 1%. In addition, 15 ng of DNA used for bisulfite conversion was required for obtaining a complete profile. The cumulative discrimination power of the panel among the Han population of northern China could reach 0.999983. This is the first investigation conducted for the simultaneous identification of blood and its donor regardless of other body fluids included in mixed stains. The successful construction of the panel will play a vital role in the comprehensive analysis of blood-containing mixtures in forensic practice.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Líquidos Corporales / Polimorfismo de Nucleótido Simple Límite: Female / Humans Idioma: En Revista: Int J Legal Med Asunto de la revista: JURISPRUDENCIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Líquidos Corporales / Polimorfismo de Nucleótido Simple Límite: Female / Humans Idioma: En Revista: Int J Legal Med Asunto de la revista: JURISPRUDENCIA Año: 2024 Tipo del documento: Article País de afiliación: China