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"GenderPlex" 是一种用于可靠检测降解人类 DNA 样本和复杂性别组合的 PCR 多重检测试剂盒。

"GenderPlex" a PCR multiplex for reliable gender determination of degraded human DNA samples and complex gender constellations.

机构信息

Institute of Legal Medicine, Innsbruck Medical University, Müllerstrasse 44, 6020 Innsbruck, Austria.

出版信息

Int J Legal Med. 2009 Nov;123(6):459-64. doi: 10.1007/s00414-008-0301-z. Epub 2008 Dec 17.

Abstract

The amelogenin test integrated in most commercial polymerase chain reaction (PCR) multiplex kits is routinely used in the forensic field for gender determination of DNA samples. It has been demonstrated that this test is not entirely reliable. Males with deletions in the homologous amelogenin part on the Y chromosome (AMELY) were erroneously typed as females due to lack of Y-specific amelogenin amplification. Also, primer binding site mutations that result in a failure to amplify the AMELY or the X-chromosomal part (AMELX) have been observed. For clarification of such phenomena, a new PCR multiplex (GenderPlex) is presented, co-amplifying two different regions of the amelogenin gene (55/58 and 106/112 bp for the AMELX and AMELY alleles, respectively), a 93-bp sequence stretch of the SRY gene and four mini-X-STR loci DXS7424, DXS8378, DXS6803 and GATA172D05 (maximum product size less than 140 bp). This strategy helps with the evaluation of samples for the presence of amelogenin-based primer site mutations and confirms a male genotype by the absence of heterozygote X-STR alleles and the presence of an SRY-related peak. The short amplicon sizes of all involved loci proved to be beneficial in a study on artificially degraded DNA. Furthermore, we demonstrate by means of sensitivity, human specificity and mixture studies that the multiplex is suitable for investigations in the forensic scene. Finally, the performance of the GenderPlex was evaluated on a west Eurasian population sample from Austria comprising 166 male and 104 female individuals.

摘要

该 amelogenin 测试集成在大多数商业聚合酶链反应 (PCR) 多重试剂盒中,通常用于法医领域的 DNA 样本性别鉴定。已经证明,该测试并非完全可靠。由于缺乏 Y 特异性 amelogenin 扩增,Y 染色体同源 amelogenin 部分缺失的男性(AMELY)会被错误地分型为女性。此外,还观察到导致 AMELY 或 X 染色体部分 (AMELX) 扩增失败的引物结合位点突变。为了澄清此类现象,提出了一种新的 PCR 多重(GenderPlex),共同扩增 amelogenin 基因的两个不同区域(AMELX 和 AMELY 等位基因分别为 55/58 和 106/112 bp),一个 93-bp 的 SRY 基因序列和四个 mini-X-STR 基因座 DXS7424、DXS8378、DXS6803 和 GATA172D05(最大产物大小小于 140 bp)。该策略有助于评估样品中是否存在基于 amelogenin 的引物位点突变,并通过不存在杂合 X-STR 等位基因和存在与 SRY 相关的峰来确认男性基因型。所有涉及的基因座的短扩增子大小在人工降解 DNA 的研究中被证明是有益的。此外,我们通过灵敏度、人类特异性和混合物研究证明,该多重体系适用于法医现场的研究。最后,在来自奥地利的 166 名男性和 104 名女性的西欧亚人群样本中评估了 GenderPlex 的性能。

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