Junyi Di , Jing Jin , Jinzhuan Zhang , Xiaoning Xu , Chen Li , Keli Guo , Chaoyi Shi
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A series of bloodstains were prepared under different heating conditions, and the results of short tandem repeat (STR) typing were systematically correlated with the trace characteristics of bloodstains. The findings indicate that heating bloodstains below 150 °C for less than 10 mins has minimal effect on DNA testing. After heating bloodstains at 150 °C for 20 mins or at 180 °C for 5 mins, partial DNA profiles were obtained, accompanied by blackening and cracking of the bloodstains. After exposure to 180 °C for 20 mins or 200 °C for 10 mins, no DNA profiles were obtained with bloodstains exhibiting metallic lusters and black bulges. Furthermore, from the perspective of chemical bond energy, the C-N, C-O, C-C, and P-O bonds in DNA molecules are prone to breaking during heating. The C-N bond serves as the primary connection between the four bases and the strand, while the C-O, C-C, and P-O bonds are significant connections within the DNA strand. It is thus hypothesized that the breakage of any bond aforementioned during heating results in the failure of DNA typing. Understanding the correlation between trace characteristics of bloodstains and DNA typing results after thermal exposure is crucial for comprehending DNA recovery from physical evidence collected from fire scenes.</div></div>","PeriodicalId":50435,"journal":{"name":"Forensic Science International-Genetics","volume":"74 ","pages":"Article 103172"},"PeriodicalIF":3.2000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Research on correlation between DNA typing and trace characteristics of blood after thermal exposure\",\"authors\":\"Junyi Di , Jing Jin , Jinzhuan Zhang , Xiaoning Xu , Chen Li , Keli Guo , Chaoyi Shi\",\"doi\":\"10.1016/j.fsigen.2024.103172\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The identification of biological evidence is particularly important for criminal detection, and the deoxyribonucleic acid (DNA) analysis plays a significant role in reconstructing events. However, bloodstains after thermal exposure in fires are quite unique compared to those in other scenes. Previous results regarding DNA recovery in bloodstains after heating are inconsistent with each other, which limits guidance for forensic science. In order to confirm the influence of heat on DNA recovery, the important physical evidence, bloodstain, was selected for its common occurrence, and a standard heat source, the Cone Calorimeter, was used to simulate high temperatures in fire scenes. A series of bloodstains were prepared under different heating conditions, and the results of short tandem repeat (STR) typing were systematically correlated with the trace characteristics of bloodstains. The findings indicate that heating bloodstains below 150 °C for less than 10 mins has minimal effect on DNA testing. After heating bloodstains at 150 °C for 20 mins or at 180 °C for 5 mins, partial DNA profiles were obtained, accompanied by blackening and cracking of the bloodstains. After exposure to 180 °C for 20 mins or 200 °C for 10 mins, no DNA profiles were obtained with bloodstains exhibiting metallic lusters and black bulges. Furthermore, from the perspective of chemical bond energy, the C-N, C-O, C-C, and P-O bonds in DNA molecules are prone to breaking during heating. The C-N bond serves as the primary connection between the four bases and the strand, while the C-O, C-C, and P-O bonds are significant connections within the DNA strand. It is thus hypothesized that the breakage of any bond aforementioned during heating results in the failure of DNA typing. Understanding the correlation between trace characteristics of bloodstains and DNA typing results after thermal exposure is crucial for comprehending DNA recovery from physical evidence collected from fire scenes.</div></div>\",\"PeriodicalId\":50435,\"journal\":{\"name\":\"Forensic Science International-Genetics\",\"volume\":\"74 \",\"pages\":\"Article 103172\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Forensic Science International-Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872497324001686\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Forensic Science International-Genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872497324001686","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
生物证据的鉴定对于刑事侦查尤为重要,脱氧核糖核酸(DNA)分析在重建事件中发挥着重要作用。然而,与其他场景中的血迹相比,火灾中热辐射后的血迹非常独特。以往有关加热后血迹中 DNA 恢复的结果并不一致,这限制了对法医学的指导。为了证实加热对 DNA 复原的影响,我们选择了常见的重要物证--血迹,并使用标准热源锥形量热仪模拟火灾现场的高温。在不同的加热条件下制备了一系列血迹,并将短串联重复(STR)分型结果与血迹的痕迹特征进行了系统关联。研究结果表明,在 150 °C 以下加热血迹少于 10 分钟,对 DNA 检测的影响微乎其微。将血迹在 150 ℃ 下加热 20 分钟或 180 ℃ 下加热 5 分钟后,可获得部分 DNA 图谱,同时血迹会变黑和开裂。在 180 °C 下加热 20 分钟或 200 °C 下加热 10 分钟后,没有得到 DNA 图谱,血迹呈现金属光泽和黑色隆起。此外,从化学键能的角度来看,DNA 分子中的 C-N、C-O、C-C 和 P-O 键在加热过程中容易断裂。C-N 键是四个碱基和链之间的主要连接,而 C-O、C-C 和 P-O 键是 DNA 链内部的重要连接。因此,假设上述任何键在加热过程中断裂都会导致 DNA 分型失败。了解血迹的痕迹特征与热暴露后 DNA 分型结果之间的相关性,对于理解从火灾现场收集的物证中恢复 DNA 至关重要。
Research on correlation between DNA typing and trace characteristics of blood after thermal exposure
The identification of biological evidence is particularly important for criminal detection, and the deoxyribonucleic acid (DNA) analysis plays a significant role in reconstructing events. However, bloodstains after thermal exposure in fires are quite unique compared to those in other scenes. Previous results regarding DNA recovery in bloodstains after heating are inconsistent with each other, which limits guidance for forensic science. In order to confirm the influence of heat on DNA recovery, the important physical evidence, bloodstain, was selected for its common occurrence, and a standard heat source, the Cone Calorimeter, was used to simulate high temperatures in fire scenes. A series of bloodstains were prepared under different heating conditions, and the results of short tandem repeat (STR) typing were systematically correlated with the trace characteristics of bloodstains. The findings indicate that heating bloodstains below 150 °C for less than 10 mins has minimal effect on DNA testing. After heating bloodstains at 150 °C for 20 mins or at 180 °C for 5 mins, partial DNA profiles were obtained, accompanied by blackening and cracking of the bloodstains. After exposure to 180 °C for 20 mins or 200 °C for 10 mins, no DNA profiles were obtained with bloodstains exhibiting metallic lusters and black bulges. Furthermore, from the perspective of chemical bond energy, the C-N, C-O, C-C, and P-O bonds in DNA molecules are prone to breaking during heating. The C-N bond serves as the primary connection between the four bases and the strand, while the C-O, C-C, and P-O bonds are significant connections within the DNA strand. It is thus hypothesized that the breakage of any bond aforementioned during heating results in the failure of DNA typing. Understanding the correlation between trace characteristics of bloodstains and DNA typing results after thermal exposure is crucial for comprehending DNA recovery from physical evidence collected from fire scenes.
期刊介绍:
Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.
The scope of the journal includes:
Forensic applications of human polymorphism.
Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies.
Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms.
Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications.
Non-human DNA polymorphisms for crime scene investigation.
Population genetics of human polymorphisms of forensic interest.
Population data, especially from DNA polymorphisms of interest for the solution of forensic problems.
DNA typing methodologies and strategies.
Biostatistical methods in forensic genetics.
Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches.
Standards in forensic genetics.
Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards.
Quality control.
Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies.
Criminal DNA databases.
Technical, legal and statistical issues.
General ethical and legal issues related to forensic genetics.