Børglum A D, Nyegaard M, Kvistgaard A B, Mullaart E, Uitterlinden A G, Vijg J, Kruse T A
Institute of Human Genetics and Danish Centre for Human Genome Research, Aarhus University.
Cytogenet Cell Genet. 1997;79(3-4):248-56. doi: 10.1159/000134737.
Two-dimensional (2-D) DNA typing is based on electrophoretic separation of genomic DNA fragments in two dimensions according to independent criteria (size and base-pair sequence), followed by hybridization analysis using multilocus probes. The technique allows simultaneous visualization of several hundred loci as spots in a 2-D pattern. The majority of the loci resolved are polymorphic. Using linkage analysis in a large CEPH family, this study reports the mapping of 34 loci detected by the minisatellite core probe 33.6. By multipoint linkage analysis, regional chromosome positions of the 33.6 loci could be deduced, showing no evidence of clustering. In the analysis of spot patterns, use was made of a computerized image analysis system specifically designed for 2-D DNA typing. Since experimental variations between different separation patterns were automatically corrected for with this program, rapid and reliable scorings could be obtained. The results presented demonstrate the availability of reliable genetic information throughout the 2-D separation pattern. Adding the use of semiautomated computerized pattern analysis, this study further substantiates the applicability of 2-D DNA typing in genome scanning, not only in theoretical but also in practical terms. Moreover, it can be anticipated that this method will have a specific advantage in studies that scan for trinucleotide repeat expansions and somatic instability, where the repeat sequences detected by appropriate core probes are of particular interest.
二维(2-D)DNA分型基于基因组DNA片段根据独立标准(大小和碱基对序列)在两个维度上的电泳分离,随后使用多位点探针进行杂交分析。该技术允许同时以二维模式将数百个基因座可视化为斑点。所解析的大多数基因座是多态性的。通过在一个大型CEPH家族中进行连锁分析,本研究报告了由小卫星核心探针33.6检测到的34个基因座的定位。通过多点连锁分析,可以推断出33.6基因座的区域染色体位置,未显示出聚类证据。在斑点模式分析中,使用了专门为二维DNA分型设计的计算机图像分析系统。由于该程序自动校正了不同分离模式之间的实验变化,因此可以获得快速可靠的评分。所呈现的结果证明了在整个二维分离模式中可靠遗传信息的可用性。加上使用半自动计算机模式分析,本研究进一步证实了二维DNA分型在基因组扫描中的适用性,不仅在理论上而且在实践中。此外,可以预期该方法在扫描三核苷酸重复扩增和体细胞不稳定性的研究中将具有特定优势,在这些研究中,由适当核心探针检测到的重复序列特别令人感兴趣。