Rayssiguier C, Dohet C, Radman M
Mutagenesis Laboratory, Institut Jacques Monod, Paris, France.
Biochimie. 1991 Apr;73(4):371-4. doi: 10.1016/0300-9084(91)90103-8.
Interspecific recombination in conjugation between Escherichia coli and Salmonella typhimurium is several orders of magnitude lower than intraspecies recombination and is dependent on the RecA function. This low efficiency is due to a 20% divergence in the DNA sequence. The methyl-directed (mut H,L,S dependent) mismatch repair system appears to control the fidelity of homologous recombination; inactivating one of the Mut functions increases the interspecies recombination at least by 10(3)-fold. The interspecific recombination in mutS or mutL mutants is only approximately 10-fold lower than recombination in homospecific crosses as found after correction for the efficiency of mating and DNA transfer by zygotic induction experiments. The interspecific recombination is dependent on the RecABCD pathway: it was abolished in a recA mutant and decreased approximately 10(3)-fold in a recC mutant.
大肠杆菌与鼠伤寒沙门氏菌之间接合过程中的种间重组比种内重组低几个数量级,并且依赖于RecA功能。这种低效率是由于DNA序列存在20%的差异。甲基定向(依赖于mutH、L、S)错配修复系统似乎控制着同源重组的保真度;使其中一个Mut功能失活会使种间重组至少增加10³倍。在mutS或mutL突变体中的种间重组仅比同物种杂交中的重组低约10倍,这是通过合子诱导实验校正交配和DNA转移效率后发现的。种间重组依赖于RecABCD途径:在recA突变体中它被消除,在recC突变体中它降低了约10³倍。