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Interactions of regulated and deregulated forms of the σ~(54) holoenzyme with heteroduplex promoter DNA

机译:调节型和去调节型σ〜(54)全酶与异源双链启动子DNA的相互作用

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摘要

The bacterial σ~(54) RNA polymerase holoenzyme binds to promoters as a stable closed complex that is silent for transcription unless acted upon by an enhancer-dependent σ~(54) holoenzyme to interact with promoter DNA containing various regions of heteroduplex from -12 to -1 was assessed. Different DNA regions important for stabilising σ~(54) holoenzyme-promoter interactions, destabilising binding, limiting template utilisation in activator-dependent transcription and for stable binding of a deregulated form of the holoenzyme lacking σ~(54) Region I were identified. It appears that homoduplex structures are required for early events in σ~(54) holoenzyme promoter binding and that disruption of a repressive fork junction structure only modestly deregulates transcription. DNA opening from -5 to -1 appears important for stable engagement of the holoenzyme following activation. The regulatory Region I of σ~(54) was shown to be involved in interactions with the sequences in the -5 to -1 area.
机译:细菌σ〜(54)全酶与稳定的封闭复合物结合启动子,对转录沉默,除非受增强子依赖性σ〜(54)全酶作用与包含-12异源双链体各个区域的启动子DNA相互作用到-1被评估。确定了对稳定σ〜(54)全酶启动子相互作用,不稳定的结合,限制模板在激活剂依赖性转录中的利用以及稳定结合缺乏σ〜(54)I区的失调形式的完整酶的重要DNA不同区域。似乎同源双链体结构是σ〜(54)全酶启动子结合中早期事件所必需的,而阻抑叉连接结构的破坏仅适度地解除了转录调控。从-5到-1的DNA开口对于激活后完整酶的稳定结合很重要。显示了σ〜(54)的调控区I与-5至-1区域中的序列相互作用。

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