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THE SIGMA SUBUNIT OF ESCHERICHIA COLI RNA POLYMERASE SENSES PROMOTER SPACING

机译:大肠埃希菌COLI RNA聚合酶的SIGMA子启动子

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The promoters recognized by sigma(70), the primary sigma of Escherichia coli, consist of two highly conserved hexamers located at -10 and -35 bp from the start point of transcription, separated by a preferred spacing of 17 bp, sigma factors have two distinct DNA binding domains that recognize the two hexamer sequences, However, the component of RNA polymerase recognizing the length of the spacing between hexamers has not been determined, Using an equilibrium DNA binding competition assay, we demonstrate that a polypeptide of sigma(70) carrying both DNA binding domains is very sensitive to promoter spacing, whereas a sigma(70) polypeptide with only one DNA binding domain is not, Furthermore, a mutant sigma, selected for increasing transcription of the minimal lac promoter (18-bp spacer), has an altered response to promoter spacing in vivo and in vitro. Our data support the idea that sigma makes simultaneous, productive contacts at both the -10 and the -35 regions of the promoter and discerns the spacing between these conserved regions. [References: 23]
机译:被大肠杆菌(Escherichia coli)的主要sigma(70)识别的启动子由两个高度保守的六聚体组成,这些六聚体位于转录起始点的-10和-35 bp之间,并以17 bp的优选间隔隔开,sigma因子有两个识别两个六聚体序列的不同DNA结合结构域,但是,尚未确定识别六聚体之间的间隔长度的RNA聚合酶的成分。使用平衡DNA结合竞争测定法,我们证明了sigma(70)携带的多肽这两个DNA结合结构域对启动子间距非常敏感,而只有一个DNA结合结构域的sigma(70)多肽不是,而且,选择用于增加最小lac启动子(18-bp间隔子)转录的突变sigma具有体内和体外对启动子间隔的反应改变。我们的数据支持sigma在启动子的-10和-35区域同时进行有效接触的想法,并可以看出这些保守区域之间的间隔。 [参考:23]

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