首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Probing the assembly of transcription initiation complexes through changes in σ~N protease sensitivity
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Probing the assembly of transcription initiation complexes through changes in σ~N protease sensitivity

机译:通过改变σ〜N蛋白酶敏感性来探测转录起始复合物的组装

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摘要

The alternative bacterial σ~N RNA polymer- ase holoenzyme binds promoters as a transcriptionally inac- tive complex that is activated by enhancer-binding proteins. Little is known about how sigma factors respond to their ligands or how the responses lead to transcription. To examine the liganded state of σ~N, the assembly of end-labeled Klebsiella pneumoniae σ~N into holoenzyme, closed promoter complexes, and initiated transcription complexes was analyzed by enzy- matic protein footprinting. V8 protease-sensitive sites in free σ~N were identified in the acidic region II and bordering or within the minimal DNA binding domain.
机译:备选的细菌σ〜N RNA聚合酶全酶将启动子结合为转录不活跃复合物,并被增强子结合蛋白激活。关于σ因子如何响应其配体或响应如何导致转录,人们所知甚少。为了检查σ〜N的配体状态,通过酶促蛋白质印迹法分析了末端标记的肺炎克雷伯菌σ〜N组装成全酶,封闭的启动子复合物和起始的转录复合物。在酸性区II中,在最小DNA结合域的边界或内部,发现了游离σ〜N中的V8蛋白酶敏感位点。

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