Tamaki K, Monckton D G, MacLeod A, Allen M, Jeffreys A J
Department of Genetics, University of Leicester, UK.
Hum Mol Genet. 1993 Oct;2(10):1629-32. doi: 10.1093/hmg/2.10.1629.
Minisatellite variant repeat mapping by PCR (MVR-PCR) provides a digital approach to DNA typing that can reveal huge levels of variation at minisatellite loci. MVR-PCR has so far been applied to three human minisatellites, including the hypervariable locus D1S8. Previous analysis at D1S8 was based on the discrimination of repeat unit types that differ by a single base substitution. We now show that a second polymorphic site within D1S8 repeats may be assayed simultaneously with the first to define four classes of repeat units ('four-state MVR-PCR'). This approach can also be applied to the other end of D1S8 alleles in 'reverse four-state MVR-PCR'. Both of these procedures substantially increase the informativeness of MVR analysis at D1S8 and should prove useful in studies of minisatellite biology and potentially in forensic DNA typing.
通过聚合酶链反应进行小卫星变异重复序列图谱分析(MVR-PCR)为DNA分型提供了一种数字化方法,该方法能够揭示小卫星位点上的大量变异。到目前为止,MVR-PCR已应用于三个人类小卫星,包括高变位点D1S8。之前对D1S8的分析是基于对相差单个碱基替换的重复单元类型的鉴别。我们现在表明,D1S8重复序列中的第二个多态性位点可与第一个位点同时进行检测,以定义四类重复单元(“四态MVR-PCR”)。这种方法也可应用于“反向四态MVR-PCR”中D1S8等位基因的另一端。这两种方法都显著提高了D1S8处MVR分析的信息量,并且在小卫星生物学研究以及潜在的法医DNA分型中应该会证明是有用的。