Kitamura Masashi, Kubo Seiji, Tanaka Jin, Adachi Tatsushi
Forensic Science Laboratory, Ishikawa Prefectural Police H.Q, 1-1 Kuratsuki, Kanazawa, Ishikawa, 920-8553, Japan.
Laboratory of Molecular Pharmacognosy, Division of Pharmaceutical Sciences, Graduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa, 920-1192, Japan.
Int J Legal Med. 2018 Jul;132(4):975-981. doi: 10.1007/s00414-017-1661-z. Epub 2017 Aug 12.
Screening for male-derived biological material from collected samples plays an important role in criminal investigations, especially those involving sexual assaults. We have developed a loop-mediated isothermal amplification (LAMP) assay targeting multi-repeat sequences of the Y chromosome for detecting male DNA. Successful amplification occurred with 0.5 ng of male DNA under isothermal conditions of 61 to 67 °C, but no amplification occurred with up to 10 ng of female DNA. Under the optimized conditions, the LAMP reaction initiated amplification within 10 min and amplified for 20 min. The LAMP reaction was sensitive at levels as low as 1-pg male DNA, and a quantitative LAMP assay could be developed because of the strong correlation between the reaction time and the amount of template DNA in the range of 10 pg to 10 ng. Furthermore, to apply the LAMP assay to on-site screening for male-derived samples, we evaluated a protocol using a simple DNA extraction method and a colorimetric intercalating dye that allows detection of the LAMP reaction by evaluating the change in color of the solution. Using this protocol, samples of male-derived blood and saliva stains were processed in approximately 30 min from DNA extraction to detection. Because our protocol does not require much hands-on time or special equipment, this LAMP assay promises to become a rapid and simple screening method for male-derived samples in forensic investigations.
从采集的样本中筛查男性来源的生物材料在刑事调查中,尤其是涉及性侵犯的调查中起着重要作用。我们开发了一种针对Y染色体多重复序列的环介导等温扩增(LAMP)检测方法来检测男性DNA。在61至67°C的等温条件下,0.5 ng男性DNA成功发生扩增,但高达10 ng的女性DNA未发生扩增。在优化条件下,LAMP反应在10分钟内开始扩增,并扩增20分钟。LAMP反应对低至1 pg的男性DNA水平敏感,并且由于反应时间与10 pg至10 ng范围内的模板DNA量之间存在强相关性,因此可以开发定量LAMP检测方法。此外,为了将LAMP检测方法应用于男性来源样本的现场筛查,我们评估了一种使用简单DNA提取方法和比色嵌入染料的方案,该方案通过评估溶液颜色变化来检测LAMP反应。使用该方案,从DNA提取到检测,男性来源的血液和唾液污渍样本大约需要30分钟处理。由于我们的方案不需要太多实际操作时间或特殊设备,这种LAMP检测方法有望成为法医调查中男性来源样本的快速简便筛查方法。