Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2011 Jan 1;25(1):77-88. doi: 10.1101/gad.1991811.
The bacterial RNA polymerase (RNAP) holoenzyme consists of a catalytic core enzyme (α(2)ββ'ω) in complex with a σ factor that is essential for promoter recognition and transcription initiation. During early elongation, the stability of interactions between σ and the remainder of the transcription complex decreases. Nevertheless, there is no mechanistic requirement for release of σ upon the transition to elongation. Furthermore, σ can remain associated with RNAP during transcription elongation and influence regulatory events that occur during transcription elongation. Here we demonstrate that promoter-like DNA sequence elements within the initial transcribed region that are known to induce early elongation pausing through sequence-specific interactions with σ also function to increase the σ content of downstream elongation complexes. Our findings establish σ-dependent pausing as a mechanism by which initial transcribed region sequences can influence the composition and functional properties of the transcription elongation complex over distances of at least 700 base pairs.
细菌 RNA 聚合酶(RNAP)全酶由一个催化核心酶(α(2)ββ'ω)与一个 σ 因子组成,σ 因子对于启动子识别和转录起始是必不可少的。在早期延伸过程中,σ 与转录复合物其余部分之间的相互作用稳定性降低。然而,在过渡到延伸时,没有释放 σ 的机制要求。此外,σ 可以在转录延伸过程中与 RNAP 保持关联,并影响转录延伸过程中发生的调节事件。在这里,我们证明了在初始转录区中已知通过与 σ 的序列特异性相互作用诱导早期延伸暂停的启动子样 DNA 序列元件也能够增加下游延伸复合物中的 σ 含量。我们的发现确立了 σ 依赖性暂停作为初始转录区序列可以在至少 700 个碱基对的距离上影响转录延伸复合物的组成和功能特性的机制。