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荧光假单胞菌中 GacA 控制的小 RNA 基因启动子的激活。

GacA-controlled activation of promoters for small RNA genes in Pseudomonas fluorescens.

机构信息

Département de Microbiologie Fondamentale, Université de Lausanne, Bâtiment Biophore, CH-1015 Lausanne, Switzerland.

出版信息

Appl Environ Microbiol. 2010 Mar;76(5):1497-506. doi: 10.1128/AEM.02014-09. Epub 2010 Jan 4.

Abstract

The Gac/Rsm signal transduction pathway positively regulates secondary metabolism, production of extracellular enzymes, and biocontrol properties of Pseudomonas fluorescens CHA0 via the expression of three noncoding small RNAs, termed RsmX, RsmY, and RsmZ. The architecture and function of the rsmY and rsmZ promoters were studied in vivo. A conserved palindromic upstream activating sequence (UAS) was found to be necessary but not sufficient for rsmY and rsmZ expression and for activation by the response regulator GacA. A poorly conserved linker region located between the UAS and the -10 promoter sequence was also essential for GacA-dependent rsmY and rsmZ expression, suggesting a need for auxiliary transcription factors. One such factor involved in the activation of the rsmZ promoter was identified as the PsrA protein, previously recognized as an activator of the rpoS gene and a repressor of fatty acid degradation. Furthermore, the integration host factor (IHF) protein was found to bind with high affinity to the rsmZ promoter region in vitro, suggesting that DNA bending contributes to the regulated expression of rsmZ. In an rsmXYZ triple mutant, the expression of rsmY and rsmZ was elevated above that found in the wild type. This negative feedback loop appears to involve the translational regulators RsmA and RsmE, whose activity is antagonized by RsmXYZ, and several hypothetical DNA-binding proteins. This highly complex network controls the expression of the three small RNAs in response to cell physiology and cell population densities.

摘要

Gac/Rsm 信号转导途径通过表达三个非编码小 RNA(称为 RsmX、RsmY 和 RsmZ)正向调节荧光假单胞菌 CHA0 的次生代谢、细胞外酶的产生和生物防治特性。rsmY 和 rsmZ 启动子的结构和功能在体内进行了研究。发现保守的回文上游激活序列(UAS)对于 rsmY 和 rsmZ 的表达以及 GacA 响应调节子的激活是必要的,但不是充分的。位于 UAS 和 -10 启动子序列之间的保守性差的连接区对于 GacA 依赖性 rsmY 和 rsmZ 的表达也是必需的,这表明需要辅助转录因子。参与 rsmZ 启动子激活的一个这样的因子被鉴定为 PsrA 蛋白,先前被认为是 rpoS 基因的激活子和脂肪酸降解的抑制剂。此外,整合宿主因子(IHF)蛋白被发现能够在体外与 rsmZ 启动子区域高亲和力结合,表明 DNA 弯曲有助于 rsmZ 的调控表达。在 rsmXYZ 三重突变体中,rsmY 和 rsmZ 的表达高于野生型。这种负反馈环似乎涉及翻译调节剂 RsmA 和 RsmE,其活性受到 RsmXYZ 的拮抗,以及几种假设的 DNA 结合蛋白。这个高度复杂的网络控制着三个小 RNA 的表达,以响应细胞生理学和细胞群体密度。

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