McAllister W T, Wu H L
Proc Natl Acad Sci U S A. 1978 Feb;75(2):804-8. doi: 10.1073/pnas.75.2.804.
The transcription program of bacteriophage T7 in vivo was analyzed by hybridizing T7 mRNAs, labeled at intervals after infection, to Hpa I restriction fragments of T7 DNA. Transcripcion of the late genes is temporally regulated: class II genes are transcribed between 4 and 16 min after infection; most class III genes are transcribed from 8 min after infection until lysis. Genes 8--10 are transcribed as both class II and class III genes. The rate of T7 RNA synthesis decreases sharply at 10 min after infection. The rapid decrease in the rate of T7 RNA synthesis and the shutoff of class II RNA synthesis were not observed in cells infected with phage defective in gene 3.5 (lysozyme). Although the decrease in the rate of T7 RNA synthesis is independent of DNA replication, the failure to shut off class II RNA synthesis normally in 3.5-- -infected cells may reflect the role of T7 lysozyme in DNA replication. In vitro, the regions of T7 DNA transcribed by the phage RNA polymerase were found to be dependent upon ionic conditions.
通过将感染后不同时间标记的T7信使核糖核酸(mRNA)与T7脱氧核糖核酸(DNA)的Hpa I限制性片段杂交,分析了噬菌体T7在体内的转录程序。晚期基因的转录受时间调控:II类基因在感染后4至16分钟转录;大多数III类基因在感染后8分钟开始转录直至裂解。基因8 - 10既作为II类基因也作为III类基因转录。感染后10分钟,T7核糖核酸(RNA)合成速率急剧下降。在感染有3.5基因(溶菌酶)缺陷的噬菌体的细胞中,未观察到T7 RNA合成速率的快速下降和II类RNA合成的关闭。尽管T7 RNA合成速率的下降与DNA复制无关,但在3.5感染的细胞中未能正常关闭II类RNA合成可能反映了T7溶菌酶在DNA复制中的作用。在体外,发现噬菌体RNA聚合酶转录的T7 DNA区域取决于离子条件。