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与Hin重组增强子序列和Fis-增强子复合物相关的DNA弯曲的位置、程度和方向。

Location, degree, and direction of DNA bending associated with the Hin recombinational enhancer sequence and Fis-enhancer complex.

作者信息

Perkins-Balding D, Dias D P, Glasgow A C

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

J Bacteriol. 1997 Aug;179(15):4747-53. doi: 10.1128/jb.179.15.4747-4753.1997.

Abstract

The Fis protein of Escherichia coli and Salmonella typhimurium stimulates several site-specific DNA recombination reactions, as well as transcription of a number of genes. Fis binds to a 15-bp core recognition sequence and induces DNA bending. Mutations in Fis which alter its ability to bend DNA have been shown to reduce the stimulatory activity of Fis in both site-specific recombination and transcription systems. To examine the role of DNA bending in the activity of the Fis-recombinational enhancer complex in Hin-mediated site-specific DNA inversion, we have determined the locations, degrees, and directions of DNA bends associated with the recombinational enhancer and the Fis-enhancer complex. Circular-permutation assays demonstrated that a sequence-directed DNA bend is associated with the Fis binding sites in the proximal and distal domains of the recombinational enhancer. Binding of Fis to its core recognition sequence significantly increases the degree of DNA bending associated with the proximal and distal domains. The degree of DNA bending induced by Fis binding depended on the DNA sequences flanking the core Fis binding site, with angles ranging from 42 to 69 degrees. Phasing analyses indicate that both the sequence-directed and the Fis-induced DNA bends associated with the proximal and distal domains face the minor groove of the DNA helix at the center of the Fis binding site. The positions and directions of DNA bends associated with the Fis-recombinational complex support a direct role for Fis-induced DNA bending in assembly of the active invertasome.

摘要

大肠杆菌和鼠伤寒沙门氏菌的Fis蛋白可刺激多种位点特异性DNA重组反应以及多个基因的转录。Fis与一个15bp的核心识别序列结合并诱导DNA弯曲。已表明,Fis中改变其弯曲DNA能力的突变会降低Fis在位点特异性重组和转录系统中的刺激活性。为了研究DNA弯曲在Hin介导的位点特异性DNA倒位中Fis重组增强子复合物活性中的作用,我们确定了与重组增强子和Fis-增强子复合物相关的DNA弯曲的位置、程度和方向。环形置换分析表明,序列导向的DNA弯曲与重组增强子近端和远端结构域中的Fis结合位点相关。Fis与其核心识别序列的结合显著增加了与近端和远端结构域相关的DNA弯曲程度。Fis结合诱导的DNA弯曲程度取决于Fis核心结合位点侧翼的DNA序列,角度范围为42至69度。相位分析表明,与近端和远端结构域相关的序列导向和Fis诱导的DNA弯曲都面向Fis结合位点中心处DNA螺旋的小沟。与Fis重组复合物相关的DNA弯曲的位置和方向支持Fis诱导的DNA弯曲在活性倒位体组装中的直接作用。

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