McNally L, Baird M, McElfresh K, Eisenberg A, Balazs I
Lifecodes Corp., Valhalla, New York 10595.
Appl Theor Electrophor. 1990;1(5):267-72.
The analysis of restriction fragment length polymorphisms in forensic DNA samples can be used to determine whether any two or more samples have the same biological origin. However, sometimes DNA recovered from evidentiary material, such as blood or semen stains, migrates at a different rate than an exemplar sample. This difference in migration, while maintaining the same overall pattern, produces a shift in the position of the bands. To verify that a shift in migration has occurred between evidence and exemplar samples, we have utilized two DNA probes that recognize DNA fragments that do not vary in size between individuals (monomorphic). The results obtained with this type of internal control show that differences in migration rate between exemplar and evidentiary samples can be recognized and accounted for and do not affect the ability to decide whether two patterns match. A common practice in many analytical tests, to show identity between two samples, is to test the properties of the samples individually and mixed. However, this approach is not applicable to all forensic DNA identity tests. In many cases, DNA from forensic samples may be irreversibly modified and this can alter the migration rate of the DNA samples. Thus, in a mixture of DNA from exemplar and evidence, the same polymorphic DNA fragments may not comigrate and produce a composite pattern which could lead to false exclusions.
法医DNA样本中限制性片段长度多态性的分析可用于确定任意两个或更多样本是否具有相同的生物学来源。然而,有时从诸如血迹或精液斑等证据材料中提取的DNA,其迁移速率与对照样本不同。这种迁移差异在保持整体模式相同的情况下,会使条带位置发生偏移。为了验证证据样本和对照样本之间是否发生了迁移偏移,我们使用了两种DNA探针,它们识别个体间大小不变的DNA片段(单态性片段)。使用这种内部控制获得的结果表明,对照样本和证据样本之间的迁移速率差异能够被识别和解释,并且不会影响判断两种模式是否匹配的能力。在许多分析测试中,为了显示两个样本相同,常用的做法是分别测试样本以及混合样本的特性。然而,这种方法并不适用于所有法医DNA同一性测试。在许多情况下,法医样本中的DNA可能会被不可逆地修饰,这会改变DNA样本的迁移速率。因此,在对照样本和证据样本的DNA混合物中,相同的多态性DNA片段可能不会一起迁移,从而产生一个复合模式,这可能导致错误排除。