Liebeschuetz J, Ritchie D A
J Mol Biol. 1986 Dec 20;192(4):681-92. doi: 10.1016/0022-2836(86)90021-5.
The T1 pac site has been cloned into a plasmid vector. This recombinant plasmid was tested for T1-mediated transduction efficiency in comparison with a plasmid containing the phage lambda T1-pac-like site esp-lambda, plasmids containing T1 sequences other than the pac site, and plasmids containing neither T1 sequences nor known pac sites. The data obtained indicate that there are at least two distinct mechanisms of T1-mediated plasmid transduction. One requires the presence of any T1 sequence on the plasmid and probably takes place via cointegrate formation with the homologous region of an infecting T1 genome. The other is specifically dependent on the presence of a pac site on the plasmid. Plasmids are packaged as head-to-tail multimers that have one heterogeneous molecular end and the other terminated at pac, and the direction of packaging with respect to the pac site is the same for plasmids as for T1. Possible roles of pac in plasmid packaging and their implications with regard to the packaging of phage DNA are discussed.
T1 pac位点已被克隆到质粒载体中。将该重组质粒与含有噬菌体λ T1-pac样位点esp-λ的质粒、含有pac位点以外T1序列的质粒以及既不含有T1序列也不含有已知pac位点的质粒进行比较,测试其T1介导的转导效率。所获得的数据表明,T1介导的质粒转导至少有两种不同机制。一种机制要求质粒上存在任何T1序列,可能是通过与感染性T1基因组的同源区域形成共整合体而发生。另一种机制则特别依赖于质粒上pac位点的存在。质粒被包装成头尾多聚体,其一端分子异质,另一端在pac处终止,质粒相对于pac位点的包装方向与T1相同。讨论了pac在质粒包装中的可能作用及其对噬菌体DNA包装的影响。