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The Structural Basis for Promoter −35 Element Recognition by the Group IV σ Factors

机译:IV族σ因子促进启动子−35元素识别的结构基础

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摘要

The control of bacterial transcription initiation depends on a primary σ factor for housekeeping functions, as well as alternative σ factors that control regulons in response to environmental stresses. The largest and most diverse subgroup of alternative σ factors, the group IV extracytoplasmic function σ factors, directs the transcription of genes that regulate a wide variety of responses, including envelope stress and pathogenesis. We determined the 2.3-Å resolution crystal structure of the −35 element recognition domain of a group IV σ factor, Escherichia coli σE 4, bound to its consensus −35 element, GGAACTT. Despite similar function and secondary structure, the primary and group IV σ factors recognize their −35 elements using distinct mechanisms. Conserved sequence elements of the σE −35 element induce a DNA geometry characteristic of AA/TT-tract DNA, including a rigid, straight double-helical axis and a narrow minor groove. For this reason, the highly conserved AA in the middle of the GGAACTT motif is essential for −35 element recognition by σE 4, despite the absence of direct protein–DNA interactions with these DNA bases. These principles of σE 4/−35 element recognition can be applied to a wide range of other group IV σ factors.
机译:细菌转录起始的控制取决于管家功能的主要σ因子,以及响应环境压力而控制调控因子的替代σ因子。替代性σ因子的最大,种类最多的亚组IV组胞浆外功能σ因子指导着调控多种反应(包括包膜应激和发病机制)的基因的转录。我们确定了IV组σ因子大肠杆菌σ E 4的-35元素识别域的2.3-Å分辨率晶体结构,该结构与其共识的-35元素GGAACTT绑定。尽管功能和二级结构相似,但一级和四级σ因子仍使用不同的机制识别-35元素。 σ E -35元素的保守序列元素可诱导AA / TT-tract DNA的DNA几何特征,包括刚性,直双螺旋轴和狭窄的小沟。因此,尽管没有与这些DNA碱基直接的蛋白质DNA相互作用,但GGAACTT基序中间的高度保守的AA对于σ E 4识别-35元素至关重要。 σ E 4 / -35元素识别的这些原理可以应用于广泛的其他IV组σ因子。

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