Prentki P, Binda A, Epstein A
Department of Molecular Biology, University of Geneva, Switzerland.
Gene. 1991 Jul 15;103(1):17-23. doi: 10.1016/0378-1119(91)90385-o.
We have constructed two plasmid vectors which allow selection for in vivo deletions within cloned DNA fragments. The plasmids are derivatives of pBR322 which carry the Escherichia coli rpsL (strA) gene, known to confer a dominant streptomycin (Sm)-sensitivity phenotype to the host cell, and a copy of the IS1 transposable element. Sm-resistant strains that harbor these plasmids display sensitivity to Sm. Spontaneous IS1-promoted deletions across the rpsL gene can be isolated simply by selection for Sm resistance. Hence, nested sets of deletions of a cloned DNA can be obtained and sequenced with an IS1-specific primer. Using this approach, we have determined the complete nucleotide sequence of the omega interposon [Prentki and Krisch, Gene 29 (1984) 303-313].
我们构建了两种质粒载体,可用于筛选克隆DNA片段中的体内缺失情况。这些质粒是pBR322的衍生物,携带大肠杆菌rpsL(strA)基因,已知该基因赋予宿主细胞显性链霉素(Sm)敏感表型,以及IS1转座元件的一个拷贝。携带这些质粒的Sm抗性菌株对Sm表现出敏感性。通过选择Sm抗性,可简单地分离出由IS1促进的、跨越rpsL基因的自发缺失。因此,可获得克隆DNA的嵌套缺失集,并使用IS1特异性引物进行测序。利用这种方法,我们已经确定了ω插入序列的完整核苷酸序列[普伦蒂基和克里施,《基因》29(1984)303 - 313]。