Omer C A, Cohen S N
Mol Gen Genet. 1984;196(3):429-38. doi: 10.1007/BF00436190.
We present data showing that the SLP1 plasmids found in Streptomyces lividans after mating with S. coelicolor strain A3(2) originate as deletion mutants of a 17 kb segment of the S. coelicolor chromosome. Excision of the entire 17 kb segment yields a transiently existing plasmid containing a site for integration into the chromosome of recipient SLP1- S. lividans strains at a unique locus that corresponds to the original chromosomal location of SLP1 in S. coelicolor. The deletion mutants of SLP1 lack the attachment site and/or other regions required for its integration, and thus persist in the recipient as autonomously replicating plasmids. Plasmids that contain the complete 17 kb sequence of the chromosomally integrated SLP1 segment were constructed in vitro by circularization of restriction endonuclease-generated fragments of chromosomal DNA carrying a tandemly-duplicated integrant of SLP1. Transformation of an SLP1- S. lividans strain with such plasmids results in chromosomal integration of the SLP1 sequence at the same site at which it is integrated in S. lividans cells that acquire the sequence by mating with S. coelicolor. A model for the site-specific excision and integration of SLP1 is presented.
我们提供的数据表明,与天蓝色链霉菌菌株A3(2)交配后在淡青链霉菌中发现的SLP1质粒起源于天蓝色链霉菌染色体17 kb片段的缺失突变体。切除整个17 kb片段会产生一个瞬时存在的质粒,该质粒含有一个整合位点,可整合到受体SLP1 - 淡青链霉菌菌株的染色体上的一个独特位点,该位点与SLP1在天蓝色链霉菌中的原始染色体位置相对应。SLP1的缺失突变体缺乏其整合所需的附着位点和/或其他区域,因此在受体中作为自主复制质粒持续存在。通过将携带SLP1串联重复整合体的染色体DNA的限制性内切酶产生的片段环化,在体外构建了包含染色体整合的SLP1片段完整17 kb序列的质粒。用这种质粒转化SLP1 - 淡青链霉菌菌株会导致SLP1序列在与天蓝色链霉菌交配获得该序列的淡青链霉菌细胞中整合的相同位点进行染色体整合。本文提出了一个SLP1位点特异性切除和整合的模型。