Speek M, Raff J W, Harrison-Lavoie K, Little P F, Glover D M
Department of Biochemistry, Imperial College, London, U.K.
Gene. 1988 Apr 15;64(1):173-7. doi: 10.1016/0378-1119(88)90491-x.
We describe a new phage-lambda-replicon-based cosmid vector suitable for both chromosome walking and P-element-mediated transformation in Drosophila. Its unique BamHI cloning site is flanked by the promoters for the SP6 and T7-encoded RNA polymerases, permitting the synthesis of probes complementary to the ends of the cloned inserts for library screening. The selectable marker is tet for bacterial cell transformation and neo for Drosophila transformation expressed under the control of the Drosophila hsp70 promoter.
我们描述了一种基于噬菌体λ复制子的新型黏粒载体,它适用于果蝇中的染色体步移和P因子介导的转化。其独特的BamHI克隆位点两侧是SP6和T7编码的RNA聚合酶的启动子,允许合成与克隆插入片段末端互补的探针用于文库筛选。选择标记在果蝇hsp70启动子的控制下,细菌细胞转化用tet,果蝇转化用neo。