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Initial transcribed region sequences influence the composition and functional properties of the bacterial elongation complex

机译:最初的转录区域序列会影响细菌延伸复合物的组成和功能特性

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摘要

The bacterial RNA polymerase (RNAP) holoenzyme consists of a catalytic core enzyme (α2ββ′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.
机译:细菌RNA聚合酶(RNAP)全酶由催化核心酶(α2ββ'ω)与σ因子复合而成,该因子对于启动子识别和转录启动至关重要。在早期延伸期间,σ与转录复合物其余部分之间相互作用的稳定性降低。然而,没有机械要求在过渡到伸长时释放σ。此外,σ可以在转录延伸期间与RNAP保持关联,并影响在转录延伸期间发生的调节事件。在这里,我们证明了已知转录起始区域内的启动子样DNA序列元素,通过与σ的序列特异性相互作用诱导早期延伸暂停,也起到了增加下游延伸复合体的σ含量的作用。我们的发现建立了σ依赖性停顿作为一种机制,通过该机制,初始转录区域序列可以在至少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。

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