Lockett T J, Lewy D, Holmes P, Medveczky K, Saint R
CSIRO, Division of Biomolecular Engineering, North Ryde, NSW, Australia.
Gene. 1992 May 15;114(2):187-93. doi: 10.1016/0378-1119(92)90573-8.
We describe a new vector for the P-element-mediated introduction of gene constructs into the germ line of Drosophila melanogaster. The P-element vector carries 6.8 kb of genomic DNA containing the rough gene (ro) from D. melanogaster and a polylinker (MCS) containing ten unique cloning sites. To demonstrate its utility, we have cloned into the MCS of this vector, the firefly luciferase (Luc)-encoding gene (luc) under the control of the D. melanogaster hsp70 promoter and have transformed flies with the resultant P-element. Single insertions of this element, whether in the hemizygous or homozygous condition, completely rescued the ro- mutation and directed heat-inducible synthesis of Luc mRNA and enzyme.
我们描述了一种新的载体,用于通过P因子介导将基因构建体导入黑腹果蝇的种系。该P因子载体携带6.8 kb的基因组DNA,其中包含来自黑腹果蝇的粗糙基因(ro)以及一个含有十个独特克隆位点的多克隆位点(MCS)。为了证明其效用,我们已将萤火虫荧光素酶(Luc)编码基因(luc)在黑腹果蝇hsp70启动子的控制下克隆到该载体的MCS中,并用所得的P因子转化果蝇。该元件的单插入,无论处于半合子还是纯合子状态,都能完全挽救ro突变,并指导热诱导的Luc mRNA和酶的合成。