1 State Key Laboratory of Plant Genomics, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
2 School of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China; and.
Mol Plant Microbe Interact. 2018 Mar;31(3):299-310. doi: 10.1094/MPMI-07-17-0187-R. Epub 2018 Jan 3.
MarR (multiple antibiotic resistance regulator)-family transcription factors (TFs), which regulate the expression of virulence factors and other physiological pathways in pathogenic bacteria, are regarded as ideal molecular targets for the development of novel antimicrobial strategies. In the plant bacterial pathogen Xanthomonas campestris pv. campestris, HpaR, a typical MarR-family TF, is associated with bacterial virulence, but its mechanism of virulence regulation remains unclear. Here, we dissected the HpaR regulon using high-throughput RNA sequencing and chromatin immunoprecipitation sequencing. HpaR directly or indirectly controls the expression of approximately 448 genes; it acts both as a transcriptional activator and a repressor to control the expression of downstream genes by directly binding to their promoter regions. The consensus HpaR-binding DNA motifs contain imperfect palindromic sequences similar to [G/T]CAACAATT[C/T]TTG. In-depth analysis revealed that HpaR positively modulates transcription level of the vgrR-vgrS operon that encodes an important two-component signal transduction system to sense iron depletion and regulate bacterial virulence. Epistasis analysis demonstrated that vgrR-vgrS is a core downstream component of HpaR regulation, as overexpression of vgrR restored the phenotypic deficiencies caused by a hpaR mutation. This dissection of the HpaR regulon should facilitate future studies focused on the activating mechanism of HpaR during bacterial infection.
MarR(多重抗生素耐药调节因子)家族转录因子(TFs)调节病原菌中毒力因子和其他生理途径的表达,被认为是开发新型抗菌策略的理想分子靶标。在植物细菌性病原菌丁香假单胞菌 pv. 丁香假单胞菌中,HpaR 是一种典型的 MarR 家族 TF,与细菌毒力有关,但它的毒力调节机制尚不清楚。在这里,我们使用高通量 RNA 测序和染色质免疫沉淀测序对 HpaR 调控组进行了剖析。HpaR 直接或间接控制大约 448 个基因的表达;它通过直接结合其启动子区域,作为转录激活子和抑制剂来控制下游基因的表达。HpaR 结合 DNA 模体的共识包含类似 [G/T]CAACAATT[C/T]TTG 的不完美回文序列。深入分析表明,HpaR 正向调节 vgrR-vgrS 操纵子的转录水平,该操纵子编码一个重要的双组分信号转导系统,用于感知铁耗竭并调节细菌毒力。上位性分析表明,vgrR-vgrS 是 HpaR 调控的核心下游成分,因为 vgrR 的过表达恢复了 hpaR 突变引起的表型缺陷。HpaR 调控组的剖析应该有助于未来研究集中在 HpaR 在细菌感染过程中的激活机制上。