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一种用于区分个体的实时多重单核苷酸多态性熔解分析方法。

A real-time multiplex SNP melting assay to discriminate individuals.

作者信息

Nicklas Janice A, Buel Eric

机构信息

Vermont Forensic Laboratory, Department of Public Safety, 103 S. Main St., Waterbury, VT 05671, USA.

出版信息

J Forensic Sci. 2008 Nov;53(6):1316-24. doi: 10.1111/j.1556-4029.2008.00877.x. Epub 2008 Sep 16.

Abstract

A method that quickly and inexpensively differentiates crime scene samples from multiple donors would expedite casework analysis by allowing the selection of probative items requiring comprehensive testing. This new method need not be perfectly definitive nor give a complete 13 locus short tandem repeat (STR) profile; it simply must be able to differentiate between most victim and suspect samples. We describe the development of multiplex, single nucleotide polymorphism (SNP), fluorescence resonance energy transfer-based real-time polymerase chain reaction (PCR) assays to fulfill this need. Dual probes, one fluorescently labeled and the other labeled with a quencher, are monitored during a melt analysis to reveal an increase in fluorescence, which allows the assessment of the two SNP alleles. Two alternate 6-plex assays (with and without gender determination) have been developed for the six-color RG6000 real-time instrument (Corbett Robotics, Inc.) and one seven SNP plus gender assay (performed as two 4-plex assays, one with gender the other without) have been developed for use in four/five color real-time instruments. This technique can discriminate between 95% and 99% of samples from different individuals. This assay is fast (approximately 2 h), much less expensive than STR analysis, and uses a real-time PCR instrument which is found in most forensic and molecular biology labs.

摘要

一种能够快速且低成本地区分来自多个捐赠者的犯罪现场样本的方法,将通过允许选择需要进行全面检测的 probative 项目来加快案件分析。这种新方法不必完全确定,也不必给出完整的 13 个位点短串联重复序列(STR)图谱;它只需能够区分大多数受害者和嫌疑人的样本即可。我们描述了基于多重单核苷酸多态性(SNP)、荧光共振能量转移的实时聚合酶链反应(PCR)检测方法的开发,以满足这一需求。在熔解分析过程中监测一对探针,一个用荧光标记,另一个用淬灭剂标记,以揭示荧光的增加,从而可以评估两个 SNP 等位基因。已为六色 RG6000 实时仪器(Corbett Robotics 公司)开发了两种替代的 6 重检测方法(一种含性别判定,一种不含),并为四/五色实时仪器开发了一种七 SNP 加性别检测方法(作为两种 4 重检测方法进行,一种含性别判定,另一种不含)。该技术能够区分 95%至 99%的不同个体样本。这种检测方法速度快(约 2 小时),比 STR 分析成本低得多,并且使用的实时 PCR 仪器在大多数法医和分子生物学实验室都有。

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