Kelly M T, Ferguson J A, Hoover T R
Department of Microbiology, University of Georgia, Athens, Georgia 30602, USA.
J Bacteriol. 2000 Nov;182(22):6503-8. doi: 10.1128/JB.182.22.6503-6508.2000.
Transcription by sigma(54)-RNA polymerase holoenzyme requires an activator that catalyzes isomerization of the closed promoter complex to an open complex. We examined mutant forms of Salmonella enterica serovar Typhimurium sigma(54) that were defective in transcription initiation but retained core RNA polymerase- and promoter-binding activities. Four of the mutant proteins allowed activator-independent transcription from a heteroduplex DNA template. One of these mutant proteins, L124P V148A, had substitutions in a sequence that had not been shown previously to participate in the prevention of activator-independent transcription. The remaining mutants did not allow efficient activator-independent transcription from the heteroduplex DNA template and had substitutions within a conserved 20-amino-acid segment (Leu-179 to Leu-199), suggesting a role for this sequence in transcription initiation.
由σ(54)-RNA聚合酶全酶进行的转录需要一种激活剂,该激活剂催化封闭启动子复合物异构化为开放复合物。我们研究了鼠伤寒沙门氏菌σ(54)的突变形式,这些突变体在转录起始方面存在缺陷,但保留了核心RNA聚合酶和启动子结合活性。其中四种突变蛋白允许从异源双链DNA模板进行不依赖激活剂的转录。这些突变蛋白之一,L124P V148A,在一个以前未显示参与防止不依赖激活剂转录的序列中发生了取代。其余的突变体不允许从异源双链DNA模板进行有效的不依赖激活剂的转录,并且在一个保守的20个氨基酸片段(Leu-179至Leu-199)内发生了取代,这表明该序列在转录起始中起作用。