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首页> 外文期刊>International Journal of Legal Medicine >Differential pattern of genetic variability at the DXYS156 locus on homologous regions of X and Y chromosomes in Indian population and its forensic implications
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Differential pattern of genetic variability at the DXYS156 locus on homologous regions of X and Y chromosomes in Indian population and its forensic implications

机译:印度人口X和Y染色体同源区域DXYS156位点的遗传变异差异模式及其法医学意义

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摘要

Sex determination is routinely performed in forensic casework using the amelogenin-based sex test. The human amelogenin gene resides on homologous regions of the sex chromosomes. However, a deletion in the AmelY locus may sometimes lead to gender misidentification. The pentanucleotide microsatellite DXYS156 maps to the pseudoautosomal region of both the sex chromosomes and helps in sex determination. This STR offers an advantage of being multi-allelic, with delimited and demographically restricted alleles for the X and Y chromosomes. Also, the Y-specific alleles can be discerned from their X chromosomal counterpart due to an adenine insertion in the (TAAAA)n repeat units of the STR. The present study examines the differential variation pattern at the X and Y locus of this STR in unrelated males from linguistically and geographically diverse populations of India. The study also attempts to undertake a comparison between the two sex-determining markers through validation studies. Two population samples and few validation samples which showed erroneous results for the amelogenin locus produced alleles specific to each of the sex chromosomes at the DXYS156 locus. The error rate for the amelogenin locus was observed to be 0.27% in case of the population samples and 0.5% in case of validation samples. Statistical parameters of forensic interest indicate that the DXYS156 locus is polymorphic and discriminating for the Indian population.
机译:性别确定通常使用基于釉原蛋白的性别测试在法医案件中进行。人类牙釉蛋白基因位于性染色体的同源区域。但是,AmelY基因座的缺失有时可能导致性别识别错误。五核苷酸微卫星DXYS156映射到两个性染色体的假常染色体区域,并有助于性别确定。该STR提供了多等位基因的优势,对于X和Y染色体具有定界和人口统计学上的等位基因。而且,由于在STR的(TAAAA)n重复单元中有腺嘌呤插入,可以从它们的X染色体对应物中识别出Y特异性等位基因。本研究在语言和地理上不同的印度人群中,研究了不相关男性中该STR的X和Y位点的差异变异模式。该研究还试图通过验证研究对两种性别决定标记进行比较。两个种群样本和少量验证样本显示了釉原蛋白基因座的错误结果,产生了DXYS156基因座上每个性染色体特有的等位基因。对于群体样本而言,釉原蛋白基因座的错误率观察为0.27%,而对于验证样本而言,为0.5%。法医兴趣的统计参数表明,DXYS156基因座是多态的,并且可以区分印度人群。

著录项

  • 来源
    《International Journal of Legal Medicine》 |2013年第1期|1-6|共6页
  • 作者单位

    Ministry of Home Affairs Government of India Central Forensic Science Laboratory Directorate of Forensic Science Services">(1);

    Ministry of Home Affairs Government of India Central Forensic Science Laboratory Directorate of Forensic Science Services">(1);

    Ministry of Home Affairs Government of India Central Forensic Science Laboratory Directorate of Forensic Science Services">(1);

    Ministry of Home Affairs Government of India Central Forensic Science Laboratory Directorate of Forensic Science Services">(1);

    Ministry of Home Affairs Government of India Central Forensic Science Laboratory Directorate of Forensic Science Services">(1);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sex determination; Amelogenin; DXYS156; Pentanucleotide repeat; Indian population;

    机译:性别决定;产釉蛋白DXYS156;五核苷酸重复;印度人口;

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