Bourguignon Luc, Hoste Bernadette, Boonen Tom, Vits Kathy, Hubrecht Françoise
National Institute for Criminalistics and Criminology (NICC), Microtraces Laboratory, Chaussée de Vilvorde 98-100, B-1120 Brussels, Belgium.
Forensic Sci Int Genet. 2008 Dec;3(1):27-31. doi: 10.1016/j.fsigen.2008.08.006. Epub 2008 Oct 15.
Nuclear DNA-profiling from human hairs is a well-known technique in forensic investigations, but its success rate is quite low with some hair types. As nuclear DNA (nuDNA) extracted from telogen hair roots is in short supply and is often degraded, a simple and effective method of estimating the number of nuclear DNAs in telogen roots has been developed. DAPI, a fluorescent, non-destructive DNA stain, allows the visualization of "nuclei" (DAPI-positive spots the shape and size of the human follicular cell nuclei) and does not interfere with subsequent PCR analyses. We stained 3242 telogen roots from 27 donors. Surprisingly, of the 2572 club roots without any soft tissue remnants 11% contained visible "nuclei" and 3.3% even contained many. At the same time 57% of the 670 telogen roots with soft tissue remnants did not show any fluorescent "nuclei". We analysed the STR-profile of some of the roots selected by the DAPI screening, i.e. 132 telogen roots without soft tissue remnants, with a success rate of 79%. Our proposed screening method allows the DNA laboratory to analyse nuclear DNA only in the most promising hair roots.
从人毛发中进行核DNA分析是法医调查中一项广为人知的技术,但对某些毛发类型而言,其成功率相当低。由于从休止期发根中提取的核DNA(nuDNA)数量不足且常发生降解,因此已开发出一种简单有效的方法来估算休止期发根中的核DNA数量。DAPI是一种荧光、非破坏性的DNA染色剂,可使“细胞核”(人毛囊细胞核形状和大小的DAPI阳性斑点)可视化,且不干扰后续的PCR分析。我们对来自27名捐赠者的3242根休止期发根进行了染色。令人惊讶的是,在2572根没有任何软组织残留的棒状发根中,11%含有可见的“细胞核”,甚至3.3%含有多个。与此同时,在670根带有软组织残留的休止期发根中,57%未显示任何荧光“细胞核”。我们分析了通过DAPI筛选选出的部分发根的STR图谱,即132根没有软组织残留的休止期发根,成功率为79%。我们提出的筛选方法可让DNA实验室仅对最有希望的发根进行核DNA分析。