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单倍群测定在日本人群法医线粒体DNA分析中的应用

Utility of haplogroup determination for forensic mtDNA analysis in the Japanese population.

作者信息

Asari Masaru, Umetsu Kazuo, Adachi Noboru, Azumi Jun-ichi, Shimizu Keiko, Shiono Hiroshi

机构信息

Department of Legal Medicine, Asahikawa Medical College, 2-1 Midorigaokahigashi, Asahikawa 078-8510, Japan.

出版信息

Leg Med (Tokyo). 2007 Sep;9(5):237-40. doi: 10.1016/j.legalmed.2007.01.007. Epub 2007 Apr 27.

Abstract

Sequence analysis of the hypervariable regions (HVRs) of mitochondrial DNA (mtDNA) are routinely performed in forensic casework, however, there are still issues to be resolved, such as the existence of multiple errors in published databases or the limitations of individual discrimination in certain populations. Here, we analyzed the coding region of mtDNA in detail by examining 36 haplogroup (HG)-defining single nucleotide polymorphisms (SNPs) using amplified product-length polymorphisms (APLP) method in conjunction with sequence analysis of HVR1 and HVR2 to establish a methodology for forensically reliable and practical mtDNA testing. The mtDNAs from 217 unrelated Japanese were examined and could be classified into 27 haplogroups. By combining the data of the coding region with those of HVRs, genetic diversity was slightly increased from 0.9817 to 0.9888 for HVR1/HG and from 0.9967 to 0.9970 for HVR1/HVR2/HG, as compared to the results of HVRs only. Moreover, in most cases, reliability of the HVR data could be confirmed by haplogroup motif analysis. Our mtDNA profiling method can provide reliable data in a time and cost-saving way due to the rapid and economical nature of APLP analysis.

摘要

线粒体DNA(mtDNA)高变区(HVR)的序列分析在法医案件工作中经常进行,然而,仍有一些问题有待解决,例如已发表数据库中存在多个错误或某些人群中个体识别的局限性。在此,我们通过使用扩增产物长度多态性(APLP)方法结合HVR1和HVR2的序列分析,详细分析了36个单倍群(HG)定义的单核苷酸多态性(SNP),以建立一种法医可靠且实用的mtDNA检测方法。我们检测了217名无关日本人的mtDNA,可将其分为27个单倍群。与仅HVR的结果相比,通过将编码区数据与HVR数据相结合,HVR1/HG的遗传多样性从0.9817略有增加到0.9888,HVR1/HVR2/HG的遗传多样性从0.9967增加到0.9970。此外,在大多数情况下,单倍群基序分析可以确认HVR数据的可靠性。由于APLP分析快速且经济,我们的mtDNA分型方法可以以节省时间和成本的方式提供可靠的数据。

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