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通过小卫星变异重复图谱对第二个高变位点进行数字DNA分型。

Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping.

作者信息

Neil D L, Jeffreys A J

机构信息

Department of Genetics, University of Leicester, UK.

出版信息

Hum Mol Genet. 1993 Aug;2(8):1129-35. doi: 10.1093/hmg/2.8.1129.

Abstract

Minisatellite variant repeat unit mapping by PCR (MVR-PCR) assays the interspersion pattern of variant repeat units along minisatellite alleles. Mapping such internal variation in the highly polymorphic minisatellite MS31A (locus D7S21), reveals extreme levels of allelic variability, far in excess of that detectable by allele length analysis. Flanking base substitutional polymorphisms have enabled the 5' structure of large numbers of MS31A alleles to be derived from genomic DNA by allele-specific MVR-PCR. More than 100 alleles have now been mapped and all are different. Several alleles show related internal structures and some of these provide evidence of polarity in allelic variation reminiscent of that seen at two other hypervariable minisatellites, D1S8 (MS32) and D16S309 (MS205). We also describe the diploid digital coding of MS31A, including the simultaneous coding of MS31A and a second locus, MS32, by duplex MVR-PCR, which greatly enhances the potential forensic applications of this technique.

摘要

通过聚合酶链反应进行小卫星变异重复单元定位(MVR-PCR)可分析变异重复单元沿小卫星等位基因的散布模式。对高度多态性小卫星MS31A(基因座D7S21)的这种内部变异进行定位,揭示了等位基因变异的极端水平,远远超过通过等位基因长度分析所能检测到的水平。侧翼碱基替代多态性使得能够通过等位基因特异性MVR-PCR从基因组DNA中推导大量MS31A等位基因的5'结构。目前已定位了100多个等位基因,且所有等位基因均不相同。几个等位基因显示出相关的内部结构,其中一些提供了等位基因变异极性的证据,这让人联想到在另外两个高变小卫星D1S8(MS32)和D16S309(MS205)中所观察到的情况。我们还描述了MS31A的二倍体数字编码,包括通过双链MVR-PCR对MS31A和第二个基因座MS32进行同时编码,这极大地增强了该技术在法医领域的潜在应用。

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