Hovig E, Mullaart E, Børresen A L, Uitterlinden A G, Vijg J
Department of Genetics, Norwegian Radium Hospital, Oslo.
Genomics. 1993 Jul;17(1):66-75. doi: 10.1006/geno.1993.1284.
We have analyzed tumor and lymphocyte DNA from six breast cancer patients by one- and two-dimensional DNA fingerprinting using micro- and minisatellite core probes to estimate the extent and nature of DNA alterations in tumors. Both approaches were compared regarding sensitivity in genome analysis. We find that the number of deletions and amplifications increases linearly with the number of restriction fragments analyzed using the two-dimensional approach, as compared with the number found using the more traditional one-dimensional method. A set of four micro- and minisatellite core probes resulted in a total number of approximately 70 bands per patient using one-dimensional analysis of RsaI-digested DNA. When the same DNA was analyzed with the two-dimensional approach about 300 analyzable spots were resolved. In one patient, the tumor DNA contained 11 amplified spots and 14 deleted spots when compared to the patients lymphocyte DNA. Using HaeIII-digested DNA, a maximum of 845 spots could be observed, with only three probes.
我们使用微卫星和小卫星核心探针,通过一维和二维DNA指纹图谱分析了6名乳腺癌患者的肿瘤和淋巴细胞DNA,以评估肿瘤中DNA改变的程度和性质。对这两种方法在基因组分析中的敏感性进行了比较。我们发现,与使用更传统的一维方法相比,使用二维方法分析时,缺失和扩增的数量随分析的限制性片段数量呈线性增加。使用一组四个微卫星和小卫星核心探针,对经RsaI消化的DNA进行一维分析时,每位患者总共约有70条带。当用二维方法分析相同的DNA时,可分辨出约300个可分析的斑点。在一名患者中,与患者的淋巴细胞DNA相比,肿瘤DNA包含11个扩增斑点和14个缺失斑点。使用经HaeIII消化的DNA,仅用三个探针最多可观察到845个斑点。