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一种用于同时分析双等位基因标记的法医学方法,这些标记可推断出起源于亚洲和日本群岛的 Y 染色体单倍群。

A forensic method for the simultaneous analysis of biallelic markers identifying Y chromosome haplogroups inferred as having originated in Asia and the Japanese archipelago.

机构信息

National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, 277-0882, Japan.

出版信息

Forensic Sci Int Genet. 2010 Feb;4(2):73-9. doi: 10.1016/j.fsigen.2009.06.001. Epub 2009 Jul 3.

Abstract

Information regarding the ancestral and geographical origins of biological evidence samples may be useful for crime investigators as they narrow down the possible donors of the sample. A method for simultaneous analysis of seven biallelic markers (M130, M131, M57, M125, M175, M122 and M134) was developed for forensic application. M57, M125 and M131 are included to identify haplogroups inferred as having originated in the Japanese archipelago. Our method employs allele-specific PCR and fragment analysis using fluorescently labeled primers and capillary electrophoresis. This method can be used to assign a haplogroup from both of degraded male DNA samples and DNA samples containing a mixture of female and male DNA by designing PCR primers that generate small amplicons and are highly specific for targets on the Y chromosome. A total of 1346 samples from Japanese males collected from the four major islands and Okinawa island were classified into seven Y binary haplogroups i.e., C-M130, C-M131, D-M57, D-M125, O-M175, O-M122 and O-M134, and a "no-mutation detected" group and their frequencies were 0.0617, 0.0565, 0.1441, 0.182, 0.3418, 0.11, 0.0847 and 0.0193, respectively. Samples of "no-mutation detected" were further analyzed by direct sequencing for identification of the major haplogroup to which they belong. Along with the haplogroup data, we report haplotype data for the 16 Y-STR markers included in the AmpFlSTR Yfiler PCR amplification kit (Applied Biosystems). These data will be useful in the prediction of haplogroups based on Y-STR haplotypes.

摘要

有关生物证据样本的祖先和地理起源的信息对于犯罪调查员来说可能很有用,因为他们可以缩小样本可能的供体范围。本文开发了一种用于法医应用的同时分析七个双等位基因标记(M130、M131、M57、M125、M175、M122 和 M134)的方法。M57、M125 和 M131 被包括在内,以鉴定推断起源于日本列岛的单倍群。我们的方法采用等位基因特异性 PCR 和片段分析,使用荧光标记引物和毛细管电泳。通过设计产生小扩增子且对 Y 染色体上的靶标具有高度特异性的 PCR 引物,该方法可用于从降解的男性 DNA 样本和包含女性和男性 DNA 混合物的 DNA 样本中分配单倍群。从四大岛屿和冲绳岛收集的 1346 名日本男性样本被分为七个 Y 双等位基因单倍群,即 C-M130、C-M131、D-M57、D-M125、O-M175、O-M122 和 O-M134 以及“未检测到突变”组,其频率分别为 0.0617、0.0565、0.1441、0.182、0.3418、0.11、0.0847 和 0.0193。进一步对“未检测到突变”的样本进行直接测序分析,以确定其所属的主要单倍群。除了单倍群数据外,我们还报告了 AmpFlSTR Yfiler PCR 扩增试剂盒(Applied Biosystems)中包含的 16 个 Y-STR 标记的单倍型数据。这些数据将有助于根据 Y-STR 单倍型预测单倍群。

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