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一种新型快速检测方法的开发与验证:一种19重短串联重复序列分型系统

Development and Validation of a Novel and Fast Detection Method for : A 19-Plex Short Tandem Repeat Typing System.

作者信息

Xia Ruocheng, Tao Ruiyang, Qu Yiling, Zhang Xiaochun, Yu Huan, Yuan Chunyan, Zhang Suhua, Li Chengtao

机构信息

Academy of Forensic Sciences, Ministry of Justice, Shanghai, China.

School of Forensic Medicine, Shanxi Medical University, Taiyuan, China.

出版信息

Front Plant Sci. 2022 Feb 28;13:837945. doi: 10.3389/fpls.2022.837945. eCollection 2022.

Abstract

In recent years, influenced by the legalization of in some countries and regions, the number of people who smoke or abuse has continuously grown, cases of transnational trafficking have also been increasing. Therefore, fast and accurate identification and source tracking of have become urgent social needs. In this study, we developed a new 19-plex short tandem repeats (STRs) typing system for , which includes 15 autosomal STRs (D02-CANN1, C11-CANN1, 4910, B01-CANN1, E07-CANN1, 9269, B05-CANN1, H06-CANN2, 5159, nH09, CS1, ANUCS 305, 3735, and ANUCS 302 and 9043), two X-chromosome STRs (ANUCS 501 and 1528), one sex-determining marker (DM016, on Y-chromosome), and a quality control marker (DM029, on autosome). The whole polymerase chain reaction (PCR) process could finish within 1 h, making the system suitable for fast detection. The PCR products were detected and separated with an Applied Biosystems 3500 Genetic Analyser. Developmental validation studies indicated that the 19-plex typing system was accurate, reliable and sensitive, which could also deconvolute mixed samples. Specifically, the sensitivity study showed that a full genotyping profile was obtainable with as low as 125 pg of DNA. The species specificity study demonstrated that this multiplex has no cross-reactivity with common non DNA. In the population study, a total of 162 alleles at 15 autosomal STRs and 14 alleles at two X-chromosome STRs were detected among 85 samples. The efficiency parameters, including the total discrimination power (TDP) and the combined power of exclusion (CPE) of the system, were calculated to exceed 0.999 999 999 999 988 and 0.998 455 889 684 078, respectively, further proving that the system could meet the needs of individual identification. To the extent of the known studies, this is the first study that included the sex-determining marker. In conclusion, the developed new 19-plex STR typing system can successfully achieve the purposes of species identification, gender determination, and individual identification, which could be a powerful tool in tracing trade routes of particular drug syndicates or dealers or in linking certain to a crime scene.

摘要

近年来,受一些国家和地区相关物品合法化的影响,吸食或滥用该物品的人数持续增长,跨国该物品贩运案件也不断增加。因此,快速准确地识别和追踪该物品的来源已成为紧迫的社会需求。在本研究中,我们开发了一种新的针对该物品的19重短串联重复序列(STRs)分型系统,其中包括15个常染色体STRs(D02 - CANN1、C11 - CANN1、4910、B01 - CANN1、E07 - CANN1、9269、B05 - CANN1、H06 - CANN2、5159、nH09、CS1、ANUCS 305、3735以及ANUCS 302和9043)、两个X染色体STRs(ANUCS 501和1528)、一个性别决定标记(DM016,位于Y染色体上)以及一个质量控制标记(DM029,位于常染色体上)。整个聚合酶链反应(PCR)过程可在1小时内完成,使得该系统适用于快速检测。PCR产物用Applied Biosystems 3500基因分析仪进行检测和分离。开发验证研究表明,该19重分型系统准确、可靠且灵敏,还能对混合的该物品样本进行解卷积分析。具体而言,灵敏度研究表明,低至125 pg的该物品DNA即可获得完整的基因分型图谱。物种特异性研究表明,该多重检测与常见的非该物品DNA无交叉反应。在群体研究中,在85个样本中检测到15个常染色体STRs的162个等位基因以及两个X染色体STRs的14个等位基因。计算了该系统的效率参数,包括总鉴别力(TDP)和联合排除力(CPE),分别超过0.999 999 999 999 988和0.998 455 889 684 078,进一步证明该系统能够满足个体识别的需求。就已知研究而言,这是第一项纳入该物品性别决定标记的研究。总之,所开发的新的19重STR分型系统能够成功实现物种鉴定、性别判定和个体识别的目的,可成为追踪特定毒品犯罪集团或毒贩贸易路线或将某些该物品与犯罪现场关联起来的有力工具。

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