Hussey C, Pero J, Shorenstein R G, Losick R
Proc Natl Acad Sci U S A. 1972 Feb;69(2):407-11. doi: 10.1073/pnas.69.2.407.
Two kinds of hybridization competition experiments show that Bacillus subtilis RNA polymerase synthesizes ribosomal RNA (rRNA) in vitro with B. subtilis DNA as a template. First, RNA synthesized in vitro competes with the hybridization of [(32)P]rRNA synthesized in vivo to the heavy strand of B. subtilis DNA. Second, unlabeled rRNA synthesized in vivo competes with the hybridization of [(3)H]RNA synthesized in vitro to denatured DNA or heavy-strand DNA, but not to light-strand DNA. The ability of RNA polymerase holoenzyme to synthesize rRNA in vitro is not lost after extensive purification. RNA polymerase core enzyme, however, which is missing the sigma factor, synthesizes little rRNA in vitro.RNA polymerase purified from wild-type sporulating cells synthesizes little rRNA in vitro, while the in vitro synthesis of rRNA by RNA polymerase from stationary phase cells of the sporulation-defective mutant rfr 10 is apparently unimpaired.
两种杂交竞争实验表明,枯草芽孢杆菌RNA聚合酶以枯草芽孢杆菌DNA为模板在体外合成核糖体RNA(rRNA)。首先,体外合成的RNA与体内合成的[(32)P]rRNA与枯草芽孢杆菌DNA重链的杂交进行竞争。其次,体内合成的未标记rRNA与体外合成的[(3)H]RNA与变性DNA或重链DNA的杂交进行竞争,但不与轻链DNA竞争。RNA聚合酶全酶在体外合成rRNA的能力在广泛纯化后不会丧失。然而,缺少σ因子的RNA聚合酶核心酶在体外合成的rRNA很少。从野生型产孢细胞中纯化的RNA聚合酶在体外合成的rRNA很少,而来自产孢缺陷突变体rfr 10的稳定期细胞的RNA聚合酶在体外合成rRNA显然未受损害。