Phillips C, Parson W, Amigo J, King J L, Coble M D, Steffen C R, Vallone P M, Gettings K B, Butler J M, Budowle B
Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Santiago de Compostela, Spain.
Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria; Forensic Science Program, The Pennsylvania State University, PA, USA.
Forensic Sci Int Genet. 2016 Jul;23:19-24. doi: 10.1016/j.fsigen.2016.03.002. Epub 2016 Mar 9.
In the process of establishing short tandem repeat (STR) sequence variant nomenclature guidelines in anticipation of expanded forensic multiplexes for massively parallel sequencing (MPS), it was discovered that the STR D5S2500 has multiple positions and genomic characteristics reported. This ambiguity is because the marker named D5S2500 consists of two different microsatellites forming separate components in the capillary electrophoresis multiplexes of Qiagen's HDplex (Hilden, Germany) and AGCU ScienTech's non-CODIS STR 21plex (Wuxi, Jiangsu, China). This study outlines the genomic details used to identify each microsatellite and reveals the D5S2500 marker in HDplex has the correctly assigned STR name, while the D5S2500 marker in the AGCU 21plex, closely positioned a further 1643 nucleotides in the human reference sequence, is an unnamed microsatellite. The fact that the D5S2500 marker has existed as two distinct STR loci undetected for almost ten years, even with reported discordant genotypes for the standard control DNA, underlines the need for careful scrutiny of the genomic properties of forensic STRs, as they become adapted for sequence analysis with MPS systems. We make the recommendation that precise chromosome location data must be reported for any forensic marker under development but not in common use, so that the genomic characteristics of the locus are validated to the same level of accuracy as its allelic variation and forensic performance. To clearly differentiate each microsatellite, we propose the name D5S2800 be used to identify the Chromosome-5 STR in the AGCU 21plex.
在为大规模平行测序(MPS)建立扩展法医多重检测的短串联重复序列(STR)序列变异命名指南的过程中,发现STR D5S2500有多个已报道的位置和基因组特征。这种模糊性是因为名为D5S2500的标记由两个不同的微卫星组成,在Qiagen公司的HDplex(德国希尔德)和AGCU ScienTech公司的非CODIS STR 21plex(中国江苏无锡)的毛细管电泳多重检测中形成单独的组分。本研究概述了用于识别每个微卫星的基因组细节,并揭示HDplex中的D5S2500标记具有正确指定的STR名称,而AGCU 21plex中的D5S2500标记在人类参考序列中进一步定位了1643个核苷酸,是一个未命名的微卫星。即使标准对照DNA的基因型存在不一致报道,D5S2500标记作为两个不同的STR位点未被检测到近十年这一事实,强调了在法医STR适应MPS系统进行序列分析时,仔细审查其基因组特性的必要性。我们建议,对于任何正在开发但尚未普遍使用的法医标记,必须报告精确的染色体定位数据,以便将该位点的基因组特征验证到与其等位基因变异和法医性能相同的准确水平。为了清楚地区分每个微卫星,我们建议使用名称D5S2800来识别AGCU 21plex中的5号染色体STR。