Nolan J M, Lee M P, Wyckoff E, Hsieh T S
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3664-8. doi: 10.1073/pnas.83.11.3664.
We have isolated the gene coding for the Drosophila type II DNA topoisomerase by immunochemically screening a Drosophila cDNA library constructed with a phage lambda expression vector, lambda gt11. The identity of the cloned gene is confirmed by the analysis of an antigenic fusion protein produced in Escherichia coli and by the in vitro translation of its RNA. The gene is 5.1 kilobases in length, the expected size for a gene encoding topoisomerase II (Mr 170,000), and it is divided into five exons. By in situ hybridization to the polytene chromosomes from salivary glands, we have mapped it to chromosome 2L at 37D.
我们通过免疫化学筛选用噬菌体λ表达载体λgt11构建的果蝇cDNA文库,分离出了编码果蝇II型DNA拓扑异构酶的基因。通过对大肠杆菌中产生的抗原融合蛋白的分析以及对其RNA的体外翻译,证实了克隆基因的身份。该基因长度为5.1千碱基,这是编码拓扑异构酶II(分子量170,000)的基因的预期大小,它被分为五个外显子。通过与唾液腺的多线染色体进行原位杂交,我们将其定位到2L染色体的37D处。