Youderian P, Sugiono P, Brewer K L, Higgins N P, Elliott T
Department of Biological Sciences, University of Southern California, Los Angeles 90089-1481.
Genetics. 1988 Apr;118(4):581-92. doi: 10.1093/genetics/118.4.581.
Hybrid genetic elements, Mud-P and Mud-Q (collectively, Mud-P22s), have been constructed that carry two-thirds of the temperate Salmonella phage P22 genome sandwiched between the ends of transposon Mu. Insertions of these elements in the Salmonella chromosome generate locked-in P22 prophages that cannot excise. Upon induction (as a consequence of the inactivation of P22 c2 repressor), a locked-in prophage replicates its DNA in situ, resulting in the amplification of neighboring regions of the chromosome and the processive packaging of three contiguous headsful of adjacent DNA in one direction from the P22 packaging site, pac. Phage particles in an induced lysate of a Mud-P22 lysogen contain DNA molecules corresponding to several minutes of chromosomal DNA adjacent to the site of prophage insertion and transduce nearby genetic markers with high efficiencies. Mud-P22 prophages have been introduced into an F' episome by transposition; resident Mud insertions on the Salmonella chromosome may be converted to Mud-P22 insertions by homologous recombination in P22-mediated transductional crosses.
构建了杂种遗传元件Mud-P和Mud-Q(统称Mud-P22),它们携带三分之二的温和型沙门氏菌噬菌体P22基因组,夹在转座子Mu的两端之间。这些元件插入沙门氏菌染色体后会产生无法切离的锁定P22原噬菌体。诱导后(由于P22 c2阻遏物失活),锁定的原噬菌体在原位复制其DNA,导致染色体邻近区域扩增,并从P22包装位点pac沿一个方向进行性包装三个连续的满头部相邻DNA。Mud-P22溶原菌诱导裂解物中的噬菌体颗粒含有与原噬菌体插入位点相邻的几分钟染色体DNA对应的DNA分子,并能高效转导附近的遗传标记。通过转座将Mud-P22原噬菌体引入F'附加体;沙门氏菌染色体上的常驻Mud插入可通过P22介导的转导杂交中的同源重组转化为Mud-P22插入。