Beck L Lauren, Smith Todd G, Hoover Timothy R
Department of Microbiology, University of Georgia, Athens, GA 30602, USA.
Trends Microbiol. 2007 Dec;15(12):530-7. doi: 10.1016/j.tim.2007.09.008. Epub 2007 Nov 9.
Transcriptional activation in bacteria usually involves an activator protein that binds to sites near the target promoter. Some activators of sigma(54)-RNA polymerase holoenzyme, however, can stimulate transcription even when their DNA-binding domains are removed. Recent studies have revealed examples of sigma(54)-dependent activators that naturally lack DNA-binding domains and seem to activate transcription from solution rather than from specific DNA sites. In addition, some activators that function with other forms of RNA polymerase holoenzyme, including Bacillus subtilis Spx and the bacteriophage N4 single-stranded DNA-binding protein, also stimulate transcription without binding to DNA. Because binding to regulatory sites enables activators to stimulate transcription from specific promoters, alternative strategies for achieving specificity are required for activators that do not bind to DNA.
细菌中的转录激活通常涉及一种激活蛋白,该蛋白与靶启动子附近的位点结合。然而,一些σ⁵⁴-RNA聚合酶全酶的激活剂,即使其DNA结合结构域被去除,也能刺激转录。最近的研究揭示了一些依赖σ⁵⁴的激活剂的例子,这些激活剂天然缺乏DNA结合结构域,似乎是从溶液中而非特定DNA位点激活转录。此外,一些与其他形式的RNA聚合酶全酶起作用的激活剂,包括枯草芽孢杆菌Spx和噬菌体N4单链DNA结合蛋白,也能在不与DNA结合的情况下刺激转录。由于与调控位点的结合使激活剂能够从特定启动子刺激转录,因此对于不与DNA结合的激活剂来说,需要有实现特异性的替代策略。