Shleser R, Puga A, Tessman E S
J Virol. 1969 Oct;4(4):394-9. doi: 10.1128/JVI.4.4.394-399.1969.
Gene IV mutants of bacteriophage S13 are known to be blocked in infectious replicative form (RF) DNA synthesis, producing only a small fraction of the RF formed by wild-type phage. This investigation shows that gene IV mutants form only parental RF and are blocked in the synthesis of any progeny RF, either infectious or noninfectious. This was determined by density labeling of RF in cells treated with mitomycin C to suppress host deoxyribonucleic acid (DNA) synthesis. RF synthesis was also studied in untreated cells, using methylated albumin columns to separate RF from host DNA. In this case it was also found that synthesis of progeny RF by gene IV mutants is negligible. It has been found by DNA-ribonucleic acid (RNA) hybridization experiments that gene IV mutants form at least as much or more messenger RNA than wild-type phage. Therefore, parental RF alone can form messenger RNA in appreciable amounts.
已知噬菌体S13的基因IV突变体在感染性复制型(RF)DNA合成中受阻,仅产生野生型噬菌体形成的RF的一小部分。本研究表明,基因IV突变体仅形成亲本RF,并且在任何子代RF(无论是感染性的还是非感染性的)的合成中受阻。这是通过用丝裂霉素C处理细胞以抑制宿主脱氧核糖核酸(DNA)合成来对RF进行密度标记确定的。还使用甲基化白蛋白柱从未处理的细胞中分离RF,对RF合成进行了研究。在这种情况下,还发现基因IV突变体产生子代RF的合成可以忽略不计。通过DNA-核糖核酸(RNA)杂交实验发现,基因IV突变体形成的信使RNA至少与野生型噬菌体一样多或更多。因此,仅亲本RF就能形成相当数量的信使RNA。