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Transcription activation at promoters carrying tandem DNA sites for the Escherichia coli cyclic AMP receptor protein: Organisation of the RNA polymerase alpha subunits

机译:在带有大肠杆菌环状AMP受体蛋白质的串联DNA位点的启动子上的转录激活:RNA聚合酶α亚基的组织

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摘要

We have constructed a family of promoters carrying tandem DNA sites for the Escherichia coli cyclic AMP receptor protein (CRP), with one of the sites centred between base-pairs 41 and 42 upstream from the transcription start site, and the second site located further upstream. In vivo activity measurements show that the activity of these promoters is completely dependent on CRP and that, depending on the precise location, CRP bound at the upstream site increases transcription activation. Hydroxyl radical footprinting was exploited to investigate the binding of CRP and RNA polymerase holoenzyme (RNAP) to these promoters. The study shows that the C-terminal domains of the RNAP alpha subunits bind adjacent to the upstream CRP and that their Precise positioning depends on the location of upstream-bound CRP. The C-terminal domains of the RNAP alpha subunits interact with both the upstream and downstream-bound CRP via activating region 1 of CRP. (C) 1998 Academic Press Limited . [References: 32]
机译:我们已经构建了一个带有大肠杆菌环状AMP受体蛋白(CRP)的串联DNA位点的启动子家族,其中一个位点位于转录起始位点上游的碱基对41和42之间,第二个位点位于上游。体内活性测量表明,这些启动子的活性完全取决于CRP,并且取决于精确的位置,结合在上游位点的CRP增加了转录激活。利用羟基自由基足迹研究了CRP和RNA聚合酶全酶(RNAP)与这些启动子的结合。研究表明,RNAPα亚基的C末端结构域与上游CRP相邻结合,并且它们的精确定位取决于上游结合CRP的位置。 RNAP alpha亚基的C末端结构域通过激活CRP的区域1与上游和下游结合的CRP相互作用。 (C)1998 Academic Press Limited。 [参考:32]

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