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快速筛选常规 DNA 分析中的美洲原住民线粒体和 Y 染色体单倍群检测。

Rapid screening for Native American mitochondrial and Y-chromosome haplogroups detection in routine DNA analysis.

机构信息

Servicio de Huellas Digitales Genéticas y Cátedra de Genética y Biología Molecular, School of Pharmacy and Biochemistry, Buenos Aires University, Argentina.

出版信息

Forensic Sci Int Genet. 2011 Mar;5(2):105-8. doi: 10.1016/j.fsigen.2010.08.018. Epub 2010 Sep 28.

Abstract

Aiming to detect individuals of Native American maternal or paternal ancestry a rapid screening approach has been developed. Its strategy was based on SNP typing by Real Time PCR (rt-PCR) followed by High Resolution Melting analysis (HRM). After extraction, DNA was quantitated by rt-PCR using commercial kits; samples were then submitted to two multiplex reactions in order to determine the major Native American mtDNA and Y-chromosome haplogroups by HRM. One cocktail included primers flanking nucleotide substitutions that define mtDNA haplogroup C and sub-haplogroups A2, B2, and D1. The other included primers flanking Y-SNPs M3, M269 and U179 that allowed discriminating Q and non-Q haplogroups. In all cases amplicons were <125 nucleotides long in order to increase the peak resolution. The accuracy of the results obtained was established by means of sequencing analysis of the amplicons. The new working-flow here proposed facilitates and speeds-up the screening process that may preclude a detailed sequencing analysis of particular samples, or for further molecular epidemiological investigations in which continental origin influences might be relevant.

摘要

为了检测个体的美洲原住民母系或父系血统,我们开发了一种快速筛选方法。其策略基于 SNP 分型的实时 PCR (rt-PCR),然后是高分辨率熔解分析 (HRM)。提取 DNA 后,使用商业试剂盒通过 rt-PCR 定量;然后将样品提交给两个多重反应,以通过 HRM 确定主要的美洲原住民 mtDNA 和 Y 染色体单倍群。一种混合物包括侧翼核苷酸取代的引物,这些取代定义了 mtDNA 单倍群 C 及其亚单倍群 A2、B2 和 D1。另一种混合物包括侧翼 Y-SNPs M3、M269 和 U179 的引物,这些引物允许区分 Q 和非 Q 单倍群。在所有情况下,扩增子都<125 个核苷酸长,以提高峰分辨率。通过对扩增子进行测序分析,确定了所获得结果的准确性。这里提出的新工作流程简化并加快了筛选过程,这可能会排除对特定样品的详细测序分析,或者在可能涉及大陆起源影响的进一步分子流行病学研究中。

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