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首页> 外文期刊>Nucleic Acids Research >DNA bending and expression of the divergent nagE-B operons.
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DNA bending and expression of the divergent nagE-B operons.

机译:DNA弯曲和不同nagE-B操纵子的表达。

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Repression of the divergent nagE - B operons requires NagC binding to two operators which overlap the nagE and nagB promoters, resulting in formation of a DNA loop. Binding of the cAMP/CAP activator to its site, adjacent to the nagE operator, stabilizes the DNA loop in vitro. The DNA of the nagE-B intergenic region is intrinsically bent, with the bend centred on the CAP site. We show that displacement of the CAP site by 6 bp results in complete derepression of the two operons. This derepression is observed even in the absence of cAMP/CAP binding and despite the fact that the two NagC operators are still in phase, demonstrating that the inherently bent structure of the DNA loop is important for repression. Since no interaction between NagC and CAP has been detected, we propose that the role of CAP in the repression loop is architectural, stabilizing the intrinsic bend. The cAMP/CAP complex is necessary for activation of the nagE-B promoters. In this case protein-protein contacts between CAP and RNA polymerase are necessary for full activation, but at least a part of the activation is likely due to an effect of CAP binding altering DNA structure.
机译:抑制不同的nagE-B操纵子需要将NagC结合到两个与nagE和nagB启动子重叠的操纵子上,从而形成DNA环。 cAMP / CAP激活剂与其邻近nagE操纵子的位点结合,可在体外稳定DNA环。 nagE-B基因间区域的DNA本质上是弯曲的,弯曲位于CAP位点的中心。我们显示CAP站点的位移6 bp导致两个操纵子的完全抑制。即使在没有cAMP / CAP结合的情况下,尽管存在两个NagC操纵子仍在同相的事实,也观察到这种抑制作用,这表明DNA环的固有弯曲结构对于抑制作用很重要。由于未检测到NagC和CAP之间的相互作用,因此我们建议CAP在阻抑环中的作用是结构性的,从而稳定了固有弯曲。 cAMP / CAP复合物是激活nagE-B启动子所必需的。在这种情况下,CAP和RNA聚合酶之间的蛋白-蛋白接触对于完全激活是必需的,但是至少有一部分激活可能是由于CAP结合改变DNA结构的作用。

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