Voelkel-Meiman K, DiNardo S, Sternglanz R
Gene. 1986;42(2):193-9. doi: 10.1016/0378-1119(86)90296-9.
The structural gene for DNA topoisomerase II from the yeast Saccharomyces cerevisiae has been cloned. The clones were selected from a YEp13 plasmid bank of yeast DNA by complementing a temperature-sensitive mutation (top2-1) in the topoisomerase II gene, TOP2. Chromosomal integrants of the clone were derived by homologous recombination in strains lacking the 2 mu circle plasmid. Genetic analysis of these integrants indicates that we have cloned the TOP2 gene and not an extragenic suppressor. A YEp13-TOP2 hybrid plasmid integrant was used to localize the TOP2 gene to the left arm of chromosome XIV by the 2 mu circle-directed marker loss method. Results from standard meiotic mapping experiments indicate that TOP2 is about 16 centi-Morgans to the centromere proximal side of MET4. Northern blot analysis of TOP2 RNA isolated from a wild-type strain and from an rna2 mutant shows the RNA to be 4.5 kb long in both cases, thus indicating that the TOP2 gene has no large introns.
已克隆出酿酒酵母DNA拓扑异构酶II的结构基因。通过对拓扑异构酶II基因TOP2中的温度敏感突变(top2-1)进行互补,从酵母DNA的YEp13质粒文库中筛选出这些克隆。在缺乏2μm环状质粒的菌株中,通过同源重组获得该克隆的染色体整合体。对这些整合体的遗传分析表明,我们克隆的是TOP2基因,而非基因外抑制子。利用2μm环状质粒定向标记缺失法,将一个YEp13-TOP2杂交质粒整合体中的TOP2基因定位到了十四号染色体的左臂上。标准减数分裂定位实验结果表明,TOP2基因位于MET4基因着丝粒近端约16厘摩处。对从野生型菌株和rna2突变体中分离出的TOP2 RNA进行的Northern印迹分析表明,两种情况下RNA长度均为4.5kb,这表明TOP2基因没有大的内含子。