Duffy J J, Geiduschek E P
Cell. 1976 Aug;8(4):595-604. doi: 10.1016/0092-8674(76)90227-0.
The phage SPO1-modified RNA polymerase B-P can form rapidly initiating complexes with SPO1 DNA but not with heterologous phi1 DNA. The B-P enzyme binds only weakly to heterologous phi29 DNA: preincubation with phi29 DNA does not substantially slow the formation of rapidly initiating complexes between polymerase B-P and subsequently added SPO1 DNA. In contrast, B. subtilis holoenzyme and core polymerase are substantially sequestered by preincubation with phi29 DNA. The results show that at least one of the phage SPO1-coded subunits of the polymerase B-P determines selective transcription at the level of DNA binding and RNA chain initiation, weakens the binding of RNA polymerase core to heterologous DNA, and discriminates against promoter complex formation at certain promoters that are utilized by the B. subtilis holoenzyme.
噬菌体SPO1修饰的RNA聚合酶B-P能与SPO1 DNA迅速形成起始复合物,但不能与异源的phi1 DNA形成起始复合物。B-P酶与异源的phi29 DNA结合很弱:用phi29 DNA预孵育不会显著减慢聚合酶B-P与随后添加的SPO1 DNA之间快速起始复合物的形成。相反,枯草芽孢杆菌全酶和核心聚合酶通过与phi29 DNA预孵育而被大量隔离。结果表明,聚合酶B-P的噬菌体SPO1编码亚基中至少有一个在DNA结合和RNA链起始水平决定选择性转录,减弱RNA聚合酶核心与异源DNA的结合,并在枯草芽孢杆菌全酶利用的某些启动子处阻碍启动子复合物的形成。