Preobrazhenskaia E S, Klebanova L M, Budovskiĭ E I, Kriviskiĭ A S
Genetika. 1978 May;14(5):877-89.
Intracellular development of DNA-containing cd phage in the presence of O-methylhydroxylamine (in vivo mutagenesis) results in 50-fold increase of mutants in the phage progeny. The main effect is due to the mutagen presence during replication of phage DNA (within 10-20 min after the infection). The presence of the mutagen both before and after DNA replication does not produce any considerable mutagenic effect. Comparison of the data obtained with kinetic reaction of O-methylhydroxylamine with nucleic acid components is due to enzymatic formation of modified precursors, N4-metoxycytidine and/or N6-metoxyadenosine derivatives, which have dual functional specificity, and to their incorporation into genome under DNA replication. The presence of O-methylhydroxylamine increases not only the number of mixed clones with a high content of mutants, but also the number of pure mutant clones. Recombinogenic activity of O-methylhydroxylamine is considered to be a possible cause of this effect.
在存在O-甲基羟胺的情况下(体内诱变),含DNA的cd噬菌体的细胞内发育导致噬菌体后代中的突变体增加50倍。主要效应是由于诱变剂在噬菌体DNA复制期间(感染后10 - 20分钟内)存在。在DNA复制之前和之后诱变剂的存在不会产生任何显著的诱变效应。将所得数据与O-甲基羟胺与核酸成分的动力学反应进行比较,这是由于修饰前体N4-甲氧基胞苷和/或N6-甲氧基腺苷衍生物的酶促形成,它们具有双重功能特异性,并在DNA复制时掺入基因组。O-甲基羟胺的存在不仅增加了高突变体含量的混合克隆的数量,也增加了纯突变体克隆的数量。O-甲基羟胺的重组活性被认为是这种效应的一个可能原因。