Mailhammer R, Yang H L, Reiness G, Zubay G
Proc Natl Acad Sci U S A. 1975 Dec;72(12):4928-32. doi: 10.1073/pnas.72.12.4928.
After T4 bacteriophage infection of E. coli a complex series of events take place in the bacterium, including gross inhibition of host transcription and discrete changes in the classes of the genes of T4 that are transcribed. Accompanying these changes in the pattern of transcription one finds T4-induced changes in the RNA polymerase (EC 2.7.7.6; nucleosidetriphosphate:RNA nucleotidyltransferase). The effects of modified polymerase on transcription can be advantageously analyzed in a DNA-directed cell-free system for protein synthesis. In this system gene activity is measured indirectly by the amounts and types of proteins sythesized. In the DNA-directed cell-free system this modified polymerase, like normal polymerase, transcribes T4 DNA with a high efficiency but transcribes bacteriophage lambda and host DNA very poorly. Polymerase reconstruction experiments show that modification of the alpha subunit of the RNA polymerase is sufficient for inhibition of host transcription. Host transcription is also inhibited in vitro by T4 DNA. This latter type of inhibition is presumed to involve competition between host DNA and T4 DNA for some factor essential for transcription. The T4-modified polymerase transcribes from T4 DNA many of the same genes as normal unmodified polymerase; it also shows a capability for transcribing certain "non-early" T4 genes which is enhanced in the presence of protein-containing extracts from T4-infected cells.
T4噬菌体感染大肠杆菌后,细菌内会发生一系列复杂事件,包括宿主转录受到严重抑制以及T4转录基因类别发生离散变化。伴随着转录模式的这些变化,人们发现RNA聚合酶(EC 2.7.7.6;核苷三磷酸:RNA核苷酸转移酶)也出现了T4诱导的变化。在用于蛋白质合成的DNA指导无细胞系统中,可以有利地分析修饰后的聚合酶对转录的影响。在这个系统中,基因活性通过合成的蛋白质的数量和类型来间接测量。在DNA指导无细胞系统中,这种修饰后的聚合酶与正常聚合酶一样,能高效转录T4 DNA,但对噬菌体λ和宿主DNA的转录能力很差。聚合酶重建实验表明,RNA聚合酶α亚基的修饰足以抑制宿主转录。T4 DNA在体外也能抑制宿主转录。推测后一种抑制类型涉及宿主DNA和T4 DNA之间对转录所需某些因子的竞争。T4修饰后的聚合酶与正常未修饰的聚合酶一样,能从T4 DNA转录许多相同的基因;它还表现出转录某些“非早期”T4基因的能力,在存在来自T4感染细胞的含蛋白质提取物时,这种能力会增强。