Alvarez-Iglesias V, Jaime J C, Carracedo A, Salas A
Unidade de Xenética, Instituto de Medicina Legal, Facultad de Medicina, Universidad de Santiago de Compostela, Santiago de Compostela 15782, Galicia, Spain.
Forensic Sci Int Genet. 2007 Mar;1(1):44-55. doi: 10.1016/j.fsigen.2006.09.001. Epub 2006 Nov 29.
We have developed a single PCR multiplex SNaPshot reaction that consists of 32 coding region SNPs that allows (i) increasing the discrimination power of the mitochondrial DNA (mtDNA) typing in forensic casework, and (ii) haplogroup assignments of mtDNA profiles in both human population studies (e.g. anthropological) and medical research. The selected SNPs target the East Asian phylogeny, including its Native American derived branches. We have validated this multiplex assay by genotyping a sample of East Asians (Taiwanese) and Native Americans (Argentineans). In addition to the coding SNP typing, we have sequenced the complete control region for the same samples. The genotyping results (control region plus SNaPshot profiles) are in good agreement with previous human population genetic studies (based on e.g. complete sequencing) and the known mtDNA phylogeny. We observe that the SNaPshot method is reliable, rapid, and cost effective in comparison with other techniques of multiplex SNP genotyping. We discuss the advantages of our SNP genotyping selection with respect to previous attempts, and we highlight the importance of using the known mtDNA phylogeny as a framework for SNP profile interpretation and as a tool to minimize genotyping errors.
我们开发了一种单一PCR多重SNaPshot反应,该反应包含32个编码区单核苷酸多态性(SNP),可实现以下两点:(i)提高法医案件中线粒体DNA(mtDNA)分型的鉴别能力;(ii)在人群研究(如人类学研究)和医学研究中对mtDNA图谱进行单倍群分类。所选的SNP针对东亚系统发育,包括其美洲原住民衍生分支。我们通过对一组东亚人(台湾人)和美洲原住民(阿根廷人)样本进行基因分型,验证了这种多重检测方法。除了对编码SNP进行分型外,我们还对相同样本的完整控制区进行了测序。基因分型结果(控制区加SNaPshot图谱)与先前的人群遗传学研究(例如基于全序列测序)以及已知的mtDNA系统发育情况高度一致。我们观察到,与其他多重SNP基因分型技术相比,SNaPshot方法可靠、快速且具有成本效益。我们讨论了我们的SNP基因分型选择相对于先前尝试的优势,并强调了使用已知的mtDNA系统发育作为SNP图谱解释框架以及最小化基因分型错误工具的重要性。