Cosso S, Reynolds R
Department of Human Genetics, Roche Molecular Systems, Inc., Alameda, CA., USA.
J Forensic Sci. 1995 May;40(3):424-34.
The validation of the AmpliFLP D1S80 PCR Amplification Kit for use in forensic casework was accomplished by performing all the relevant experiments outlined in the TWGDAM guidelines. Standard specimen and reproducibility studies were performed using organic and rapid DNA extraction techniques on both stain and liquid samples (blood, semen and saliva). Over 300 samples from three different populations (US Caucasians, African Americans and US Hispanics) were analyzed to determine allele and genotype frequencies. Purified DNA was mixed in defined ratios (ranging from unmixed DNA samples to 1:9 mixtures of 2 different DNA samples) prior to amplification to demonstrate that samples containing DNA from more than one individual can be detected and, in many cases, that the genotypes contributing to the mixture can be identified. Since casework samples frequently are exposed to environmental insults that can result in DNA degradation, purified DNA was degraded in the laboratory to analyze the effect of DNA fragment length on D1S80 amplification. It is crucial in the validation process to examine actual casework evidentiary material. This D1S80 kit can be used successfully by forensic scientists to amplify and type nonprobative evidentiary material, including bloodstains collected from crime scenes and rape kit materials collected for sexual assault cases. The D1S80 kit is specific to human DNA, and the D1S80 alleles are inherited according to the laws of Mendel. The sensitivity of the novel gel electrophoresis gel matrix allowed the PCR cycle number to be reduced to 29 cycles and the D1S80 kit sensitivity to be increased to 2.5 ng from the previous D1S80 Reagent Set specifications of 30 cycles and 5 ng, respectively.
通过按照TWGDAM指南中概述的所有相关实验,完成了用于法医案件工作的AmpliFLP D1S80 PCR扩增试剂盒的验证。使用有机和快速DNA提取技术,对污渍和液体样本(血液、精液和唾液)进行了标准样本和重现性研究。分析了来自三个不同人群(美国白种人、非裔美国人和美国西班牙裔)的300多个样本,以确定等位基因和基因型频率。在扩增之前,将纯化的DNA按确定的比例混合(从未混合的DNA样本到两种不同DNA样本的1:9混合物),以证明可以检测到含有来自多个个体DNA的样本,并且在许多情况下,可以识别构成混合物的基因型。由于案件工作样本经常受到可能导致DNA降解的环境损害,因此在实验室中对纯化的DNA进行了降解,以分析DNA片段长度对D1S80扩增的影响。在验证过程中,检查实际的案件工作证据材料至关重要。法医科学家可以成功使用这种D1S80试剂盒来扩增和分型非 probative证据材料,包括从犯罪现场收集的血迹和为性侵犯案件收集的强奸试剂盒材料。D1S80试剂盒对人类DNA具有特异性,并且D1S80等位基因根据孟德尔定律遗传。新型凝胶电泳凝胶基质的灵敏度使PCR循环次数减少到29次,D1S80试剂盒的灵敏度从之前D1S80试剂套装规格的30次循环和5 ng分别提高到2.5 ng。