Kirsch S, Keil R, Edelmann A, Henegariu O, Hirschmann P, LePaslier D, Vogt P H
Reproductiongenetics in Institute of Human Genetics, University of Heidelberg, Germany.
Cytogenet Cell Genet. 1996;75(2-3):197-206. doi: 10.1159/000134481.
Conventional methods of long range restriction mapping for analysis of the genomic DNA structure failed in Yq11, because single-copy DNA probes for blot hybridization analyses are rare and the rate of DNA methylation is high in this Y region. Numerous repetitive sequence blocks of unknown extensions are scattered throughout Yq11 and a patchwork of X-Y homologous DNA blocks were found by different investigators. Therefore, our approach towards a molecular analysis of this Y region reduced this complexity by performing first its molecular analysis in YAC clones mapping to Yq11. YACs contain only a part of the whole Yq11 DNA structure. In this paper, we present our first results of this approach based on quantitative blot analysis of 51 DNA loci in 67 YAC clones. The YACs were isolated from the three CEPH libraries and mapped to a contig of 13 Mb from proximal to distal Yq11 with aid of a detailed interval map. In distal Yq11, our analysis revealed the presence of local amplification events of different DNA domains. A model of their possible arrangement is presented.
用于分析基因组DNA结构的传统长程限制酶切图谱绘制方法在Yq11区域失效,原因是用于印迹杂交分析的单拷贝DNA探针稀少,且该Y区域的DNA甲基化率很高。众多延伸情况未知的重复序列块散布于整个Yq11区域,不同研究者发现了X-Y同源DNA块的拼凑情况。因此,我们对该Y区域进行分子分析的方法是,首先在定位到Yq11的酵母人工染色体(YAC)克隆中进行分子分析,从而降低这种复杂性。YAC仅包含整个Yq11 DNA结构的一部分。在本文中,我们基于对67个YAC克隆中51个DNA位点的定量印迹分析,展示了该方法的首批结果。这些YAC是从三个CEPH文库中分离出来的,并借助详细的区间图谱定位到从Yq11近端到远端的一个13 Mb的重叠群上。在Yq11远端,我们的分析揭示了不同DNA结构域存在局部扩增事件。文中给出了它们可能排列的模型。