Bouzyk M, Bryant S P, Schmitt K, Goodfellow P N, Ekong R, Spurr N K
Human Genetic Resources, Clare Hall Laboratories, South Mimms, Hertsfordshire, EN6 3LD, United Kingdom.
Genomics. 1996 Jun 1;34(2):187-92. doi: 10.1006/geno.1996.0264.
A radiation hybrid panel has been constructed for chromosome 9 using the somatic cell hybrid GM10611 as the donor cell line fused to the hamster cell line A23. The hybrid GM10611 was characterized by fluorescence in situ hybridization and reverse painting onto spreads of normal human metaphase chromosomes; it contains human chromosome 9 as the only cytogenetically detectable human material. GM10611 was irradiated with 6000 rads of X rays prior to fusion, a total of 93 independent clones were selected, and frozen stocks and DNA were prepared from each clone. These clones were screened by PCR amplification with oligonucleotide primers for sequence-tagged sites specific for 50 single-copy loci mapping to the short arm of chromosome 9. The average retention frequency of these hybrids was approximately 23%. The markers were ordered into a framework map by analyzing coretention patterns, minimizing the number of obligatory chromosome breaks, and finally confirming the order by maximum likelihood methods. A framework map ordering 27 markers with odds greater than 1000:1 was constructed. A further 16 markers that could not be uniquely placed on the map with the required support were positioned within a range of adjacent intervals.
已构建了一个用于9号染色体的辐射杂种板,使用体细胞杂种GM10611作为供体细胞系,与仓鼠细胞系A23融合。通过荧光原位杂交和反向涂染到正常人中期染色体铺片上对杂种GM10611进行了表征;它含有9号染色体作为唯一可细胞遗传学检测到的人类物质。GM10611在融合前用6000拉德的X射线进行辐照,共选择了93个独立克隆,并从每个克隆中制备了冷冻储备和DNA。用针对映射到9号染色体短臂的50个单拷贝基因座的序列标签位点的寡核苷酸引物通过PCR扩增对这些克隆进行筛选。这些杂种的平均保留频率约为23%。通过分析共保留模式、尽量减少必需的染色体断裂数量,并最终通过最大似然法确认顺序,将这些标记排列成一个框架图。构建了一个排序27个标记且优势比大于1000:1的框架图。另外16个不能以所需支持唯一地定位在图上的标记位于一系列相邻区间内。