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鉴定与布鲁氏菌 2308 毒力相关的两个小调控 RNA。

Identification of two small regulatory RNAs linked to virulence in Brucella abortus 2308.

机构信息

Department of Microbiology and Immunology, East Carolina University School of Medicine, Greenville, NC 27834, USA.

出版信息

Mol Microbiol. 2012 Jul;85(2):345-60. doi: 10.1111/j.1365-2958.2012.08117.x. Epub 2012 Jun 12.

Abstract

Hfq is an RNA-binding protein that functions in post-transcriptional gene regulation by mediating interactions between mRNAs and small regulatory RNAs (sRNAs). Two proteins encoded by BAB1_1794 and BAB2_0612 are highly over-produced in a Brucella abortus hfq mutant compared with the parental strain, and recently, expression of orthologues of these proteins in Agrobacterium tumefaciens was shown to be regulated by two sRNAs, called AbcR1 and AbcR2. Orthologous sRNAs (likewise designated AbcR1 and AbcR2) have been identified in B. abortus 2308. In Brucella, abcR1 and abcR2 single mutants are not defective in their ability to survive in cultured murine macrophages, but an abcR1 abcR2 double mutant exhibits significant attenuation in macrophages. Additionally, the abcR1 abcR2 double mutant displays significant attenuation in a mouse model of chronic Brucella infection. Quantitative proteomics and microarray analyses revealed that the AbcR sRNAs predominantly regulate genes predicted to be involved in amino acid and polyamine transport and metabolism, and Northern blot analyses indicate that the AbcR sRNAs accelerate the degradation of the target mRNAs. In an Escherichia coli two-plasmid reporter system, overexpression of either AbcR1 or AbcR2 was sufficient for regulation of target mRNAs, indicating that the AbcR sRNAs from B. abortus 2308 perform redundant regulatory functions.

摘要

Hfq 是一种 RNA 结合蛋白,通过介导 mRNA 和小调控 RNA(sRNA)之间的相互作用,在转录后基因调控中发挥作用。BAB1_1794 和 BAB2_0612 编码的两种蛋白质在布鲁氏菌 hfq 突变体中比亲本菌株大量过度产生,最近,在根癌农杆菌中这些蛋白质的同源物的表达被证明受到两种 sRNA(称为 AbcR1 和 AbcR2)的调控。在 B. abortus 2308 中也鉴定出了同源 sRNA(同样命名为 AbcR1 和 AbcR2)。在布鲁氏菌中,abcR1 和 abcR2 单突变体在其在培养的鼠巨噬细胞中存活的能力方面没有缺陷,但 abcR1 abcR2 双突变体在巨噬细胞中表现出明显的衰减。此外,abcR1 abcR2 双突变体在慢性布鲁氏菌感染的小鼠模型中显示出明显的衰减。定量蛋白质组学和微阵列分析显示,AbcR sRNA 主要调控预测与氨基酸和多胺转运和代谢相关的基因,Northern blot 分析表明 AbcR sRNA 加速了靶 mRNA 的降解。在大肠杆菌双质粒报告系统中,过表达 AbcR1 或 AbcR2 中的任何一种都足以调节靶 mRNA,表明来自 B. abortus 2308 的 AbcR sRNA 执行冗余的调节功能。

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