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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >East Asian mtDNA haplogroup determination in Koreans: Haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis
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East Asian mtDNA haplogroup determination in Koreans: Haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis

机译:韩国人中东亚mtDNA单倍群的确定:单倍群级编码区SNP分析和单倍群级控制区序列分析

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摘要

The present study analyzed 21 coding region SNP markers and one deletion motif for the determination of East Asian mitochondrial DNA (mtDNA) haplogroups by designing three multiplex systems which apply single base extension methods. Using two multiplex systems, all 593 Korean mtDNAs were allocated into 15 haplogroups: M, D, D4, D5, G, M7, M8, M9, M10, M11, R, R9, B, A, and N9. As the D4 haplotypes occurred most frequently in Koreans, the third multiplex system was used to further define D4 subhaplogroups: D4a, D4b, D4e, D4g, D4h, and D4j. This method allowed the complementation of coding region information with control region mutation motifs and the resultant findings also suggest reliable control region mutation motifs for the assignment of East Asian mtDNA haplogroups. These three multiplex systems produce good results in degraded samples as they contain small PCR products (101-154 bp) for single base extension reactions. SNP scoring was performed in 101 old skeletal remains using these three systems to prove their utility in degraded samples. The sequence analysis of mtDNA control region with high incidence of haplogroup-specific mutations and the selective scoring of highly informative coding region SNPs using the three multiplex systems are useful tools for most applications involving East Asian mtDNA haplogroup determination and haplogroup-directed stringent quality control.
机译:本研究通过设计三个应用单碱基延伸方法的多重系统,分析了21个编码区SNP标记和一个缺失基序,用于确定东亚线粒体DNA(mtDNA)单倍体。使用两个多重系统,将所有593个韩国mtDNA分为15个单倍群:M,D,D4,D5,G,M7,M8,M9,M10,M11,R,R9,B,A和N9。由于D4单体型在韩国人中最常见,因此使用了第三个多重系统进一步定义D4子单体组:D4a,D4b,D4e,D4g,D4h和D4j。该方法允许用控制区突变基序对编码区信息进行补充,结果也表明可靠的控制区突变基序可用于东亚mtDNA单倍型的分配。这三个多重系统在降解的样品中产生良好的结果,因为它们包含用于单碱基延伸反应的小PCR产物(101-154 bp)。使用这三个系统对101个旧骨骼残骸进行了SNP评分,以证明其在降解样品中的效用。使用三种多重系统对具有单倍群特异性突变发生率很高的mtDNA控制区进行序列分析以及对高信息量编码区SNP进行选择性评分是有用的工具,可用于涉及东亚mtDNA单倍群确定和单倍群指导的严格质量控制的大多数应用。

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