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用于人类性别鉴定的牙釉蛋白基因标记替代物及其法医学相关性。

Alternatives to amelogenin markers for sex determination in humans and their forensic relevance.

机构信息

DNA Fingerprinting Unit, Forensic Science Laboratory, Sagar, Madhya Pradesh, 470 001, India.

Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India.

出版信息

Mol Biol Rep. 2020 Mar;47(3):2347-2360. doi: 10.1007/s11033-020-05268-y. Epub 2020 Jan 25.

Abstract

Forensic DNA typing and subsequent molecular methods of sex determination in humans have been proven to be an imperious tool to criminal justice system. In current practice, most of the short tandem repeat (STR) based commercial kits contain amelogenin as the sexing marker. Amelogenin gene which contributes to the tooth enamel formation is present on both X and Y chromosome with a variation in base pair size. However, huge discrepancies have been observed with amelogenin based sex determination mostly due to X and Y deletion in the population and mutation in primer binding sites. Some ethnicities such as those in Indian population are affected badly with inappropriate sex determination by amelogenin marker due to the presence of high frequency of Y deletion in the population. Presence of PCR inhibitors, degradation in the DNA samples and presence of mixed DNA also contribute to the discrepancy in results obtained by amelogenin analysis. To overcome this problem, many alternative markers/techniques such as STS, SRY, TSPY, DXYS156, SNPs, DYZ1 and Next generation sequencing have been discussed in much detail with their respective pros and cons. In this regard, inclusion of one or more alternative markers along with amelogenin will decrease the anomalies in sex determination observed while using the amelogenin marker alone in forensic sample analysis.

摘要

法医 DNA 分型和随后的人类性别分子检测方法已被证明是刑事司法系统的有力工具。在当前的实践中,大多数基于短串联重复序列(STR)的商业试剂盒都包含 amelogenin 作为性别标记。amelogenin 基因参与牙釉质的形成,存在于 X 和 Y 染色体上,碱基对大小存在差异。然而,由于人群中 X 和 Y 染色体缺失以及引物结合位点突变,基于 amelogenin 的性别鉴定存在很大差异。一些族群,如印度人群,由于人群中 Y 染色体缺失频率较高,因此 amelogenin 标记的性别鉴定存在很大问题。PCR 抑制剂的存在、DNA 样本的降解以及混合 DNA 的存在也导致 amelogenin 分析结果存在差异。为了解决这个问题,已经详细讨论了许多替代标记物/技术,如 STS、SRY、TSPY、DXYS156、SNP、DYZ1 和下一代测序,以及它们各自的优缺点。在这方面,在法医样本分析中,使用 amelogenin 标记物时,单独使用 amelogenin 标记物观察到的性别鉴定异常,可以通过包含一个或多个替代标记物来减少。

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