Moretti T R, Baumstark A L, Defenbaugh D A, Keys K M, Brown A L, Budowle B
FBI Laboratory, FBI Academy, Quantico, VA 22135, USA.
J Forensic Sci. 2001 May;46(3):661-76.
With the use of capillary electrophoresis (CE), high-resolution electrophoretic separation of short tandem repeat (STR) loci can be achieved in a semiautomated fashion. Laser-induced detection of fluorescently labeled PCR products and multicolor analysis enable the rapid generation of multilocus DNA profiles. In this study, conditions for typing PCR-amplified STR loci by capillary electrophoresis were investigated using the ABI Prism 310 Genetic Analyzer (Applied Biosystems). An internal size standard was used with each run to effectively normalize mobility differences among injections. Alleles were designated by comparison to allelic ladders that were run with each sample set. Multiple runs of allelic ladders and of amplified samples demonstrate that allele sizes were reproducible, with standard deviations typically less than 0.12 bases for fragments up to 317 bases in length (largest allele analyzed) separated in a 47 cm capillary. Therefore, 99.7% of all alleles that are the same length should fall within the measurement error window of +/- 0.36 bases. Microvariants of the tetranucleotide repeats were also accurately typed by the analytical software. Alleles differing in size by one base could be resolved in two-donor DNA mixtures in which the minor component comprised > or = 5% of the total DNA. Furthermore, the quantitative data format (i.e., peak amplitude) can in some instances assist in determining individual STR profiles in mixed samples. DNA samples from previously typed cases (typed for RFLP, AmpliType PM+DQA1, and/or D1S80) were amplified using AmpFlSTR Profiler Plus and COfiler and were evaluated using the ABI Prism 310. Most samples yielded typable results. Compared with previously determined results for other loci, there were no discrepancies as to the inclusion or exclusion of suspects or victims. CE thus provides efficient separation, resolution, sensitivity and precision, and the analytical software provides reliable genotyping of STR loci. The analytical conditions described are suitable for typing samples such as reference and evidentiary samples from forensic casework.
使用毛细管电泳(CE),可以以半自动方式实现短串联重复序列(STR)位点的高分辨率电泳分离。激光诱导检测荧光标记的PCR产物和多色分析能够快速生成多位点DNA图谱。在本研究中,使用ABI Prism 310遗传分析仪(应用生物系统公司)研究了通过毛细管电泳对PCR扩增的STR位点进行分型的条件。每次运行都使用内部大小标准来有效归一化进样间的迁移率差异。通过与每个样本集一起运行的等位基因阶梯进行比较来指定等位基因。多次运行等位基因阶梯和扩增样本表明等位基因大小具有可重复性,对于在47厘米毛细管中分离的长度达317个碱基(分析的最大等位基因)的片段,标准偏差通常小于0.12个碱基。因此,所有长度相同的等位基因中有99.7%应落在±0.36个碱基的测量误差窗口内。四核苷酸重复序列的微变体也可通过分析软件准确分型。在次要成分占总DNA≥5%的双供体DNA混合物中,可以分辨出大小相差一个碱基的等位基因。此外,定量数据格式(即峰幅度)在某些情况下有助于确定混合样本中的个体STR图谱。使用AmpFlSTR Profiler Plus和COfiler对先前分型案例(针对RFLP、AmpliType PM + DQA1和/或D1S80进行分型)的DNA样本进行扩增,并使用ABI Prism 310进行评估。大多数样本产生了可分型的结果。与先前确定的其他位点结果相比,在嫌疑人或受害者的包含或排除方面没有差异。因此,毛细管电泳提供了高效的分离、分辨率、灵敏度和精密度,并且分析软件提供了可靠的STR位点基因分型。所描述的分析条件适用于对法医案件工作中的参考样本和证据样本等样本进行分型。