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DNA分型数据中观察到的明显杂合子缺陷及其在法医学应用中的意义。

Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applications.

作者信息

Chakraborty R, De Andrade M, Daiger S P, Budowle B

机构信息

Center for Demographic and Population Genetics, University of Texas Graduate School of Biomedical Sciences, Houston 77225.

出版信息

Ann Hum Genet. 1992 Jan;56(1):45-57. doi: 10.1111/j.1469-1809.1992.tb01128.x.

Abstract

Restriction fragment length polymorphisms (RFLP) analysis using the Southern blot technique can be used to recognize copy number variation of variable number of tandem repeats (VNTR) of conserved core sequences at several regions of the human genome. This new class of polymorphisms reveals a high degree of genetic variation, useful for individual identification purposes. Criticisms against forensic applications of such DNA typing data include the limitation of employing Hardy-Weinberg expectation of genotype frequencies, since several surveys indicate apparent deficiency of heterozygosity (or excess homozygosity) in comparison with Hardy-Weinberg expectations. This research postulates an alternative explanation of deficiency of apparent heterozygosity which is caused by the inability to detect extremely small-sized alleles (called 'non-detectable' alleles) due to the sensitivity of Southern gel electrophoresis. We show that the presence of 'non-detectable' alleles can produce pseudo-homozygosity and their frequencies can be predicted from the observed proportional heterozygote deficiency. Furthermore, in the covert presence of such 'non-detectable' alleles, we show that the gene-count method provides over-estimates of allele frequencies in the sample population, and hence the Hardy-Weinberg predictions of genotype frequencies avoid wrongful bias against suspects in forensic applications of DNA typing data. Applications of this theory to population data on six VNTR loci in US Caucasians and US Blacks suggest that the presence of 'non-detectable' alleles could be the major cause of apparent heterozygote deficiency, and the current approaches of predicting the population frequency of specific DNA phenotypes are practically free of the possible wrongful bias in courtroom applications of DNA typing data.

摘要

使用Southern印迹技术的限制性片段长度多态性(RFLP)分析可用于识别人类基因组多个区域中保守核心序列的可变串联重复序列(VNTR)的拷贝数变异。这类新的多态性揭示了高度的遗传变异,可用于个体识别。对这类DNA分型数据在法医学应用中的批评包括采用哈迪-温伯格基因型频率预期的局限性,因为多项调查表明,与哈迪-温伯格预期相比,杂合性明显不足(或纯合性过高)。本研究提出了一种对明显杂合性不足的替代解释,即由于Southern凝胶电泳的敏感性,无法检测到极小尺寸的等位基因(称为“不可检测”等位基因)。我们表明,“不可检测”等位基因的存在会产生假纯合性,其频率可根据观察到的比例杂合子不足来预测。此外,在这种“不可检测”等位基因隐蔽存在的情况下,我们表明基因计数法会高估样本群体中等位基因的频率,因此,在DNA分型数据的法医学应用中,哈迪-温伯格基因型频率预测可避免对嫌疑人的错误偏见。将该理论应用于美国白人和美国黑人六个VNTR位点的群体数据表明,“不可检测”等位基因的存在可能是明显杂合子不足的主要原因,目前预测特定DNA表型群体频率的方法在法庭应用DNA分型数据时几乎不存在可能的错误偏见。

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