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大肠杆菌RNA聚合酶-抗σ⁷⁰ AsiA复合物利用上游启动子接触的α-羧基末端结构域从-10/-35启动子进行转录。

The Escherichia coli RNA polymerase.anti-sigma 70 AsiA complex utilizes alpha-carboxyl-terminal domain upstream promoter contacts to transcribe from a -10/-35 promoter.

作者信息

Orsini G, Kolb A, Buc H

机构信息

Unité de Physico-Chimie des Macromolécules Biologiques, CNRS URA 1773, Département de Biologie Moléculaire, Institut Pasteur, 25 rue du Dr. Roux, 75724 Paris Cedex 15, France.

出版信息

J Biol Chem. 2001 Jun 8;276(23):19812-9. doi: 10.1074/jbc.M010105200. Epub 2001 Mar 1.

Abstract

During infection of Escherichia coli, the phage T4 early protein AsiA inhibits open complex formation by the RNA polymerase holoenzyme Efinal sigma(70) at -10/-35 bacterial promoters through binding to region 4.2 of the final sigma(70) subunit. We used the -10/-35 lacUV5 promoter to study the properties of the Efinal sigma(70). AsiA complex in the presence of the glutamate anion. Under these experimental conditions, inhibition by AsiA was significantly decreased. KMnO(4) probing showed that the observed residual transcriptional activity was due to the slow transformation of the ternary complex Efinal sigma(70). AsiA.lacUV5 into an open complex. In agreement with this observation, affinity of the enzyme for the promoter was 10-fold lower in the ternary complex than in the binary complex Efinal sigma(70).lacUV5. A tau plot analysis of abortive transcription reactions showed that AsiA binding to Efinal sigma(70) resulted in a 120-fold decrease in the second-order on-rate constant of the reaction of Efinal sigma(70) with lacUV5 and a 55-fold decrease in the rate constant of the isomerization step leading to the open complex. This ternary complex still responded to activation by the cAMP.catabolite activator protein complex. We show that compensatory Efinal sigma(70)/promoter upstream contacts involving the C-terminal domains of alpha subunits in Efinal sigma(70) become essential for the binding of Efinal sigma(70). AsiA to the lacUV5 promoter.

摘要

在大肠杆菌感染过程中,噬菌体T4早期蛋白AsiA通过与最终σ⁷⁰亚基的4.2区域结合,抑制RNA聚合酶全酶E最终σ⁷⁰在细菌 -10/-35启动子处形成开放复合物。我们使用 -10/-35 lacUV5启动子来研究E最终σ⁷⁰。AsiA复合物在谷氨酸阴离子存在下的特性。在这些实验条件下,AsiA的抑制作用显著降低。高锰酸钾探测表明,观察到的残余转录活性是由于三元复合物E最终σ⁷⁰。AsiA.lacUV5缓慢转化为开放复合物所致。与该观察结果一致,在三元复合物中酶对启动子的亲和力比在二元复合物E最终σ⁷⁰。lacUV5中低10倍。对流产转录反应的τ图分析表明,AsiA与E最终σ⁷⁰结合导致E最终σ⁷⁰与lacUV5反应的二级结合速率常数降低120倍,以及导致开放复合物的异构化步骤的速率常数降低55倍。该三元复合物仍对cAMP。分解代谢物激活蛋白复合物的激活有反应。我们表明,涉及E最终σ⁷⁰中α亚基C末端结构域的补偿性E最终σ⁷⁰/启动子上游接触对于E最终σ⁷⁰。AsiA与lacUV5启动子的结合变得至关重要。

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