Schulmeyer Kayley H, Yahr Timothy L
Department of Microbiology, University of Iowa, United States.
Department of Microbiology, University of Iowa, United States.
Curr Opin Microbiol. 2017 Apr;36:30-36. doi: 10.1016/j.mib.2017.01.009. Epub 2017 Feb 10.
Type III secretion systems (T3SS) serve as a primary anti-host defense mechanism for many Gram-negative plant and animal pathogens. T3SS production is tightly controlled and activated by host-associated signals. Although transcriptional responses represent a significant component of the activation cascade, recent studies have uncovered diverse post-transcriptional mechanisms that also contribute to T3SS production. Targets for post-transcriptional control are often AraC/XylS transcription factors that promote T3SS gene expression. Commons mechanisms of post-transcriptional regulation include direct control of either the activity of AraC/XylS transcription factors by protein ligands, small molecules, or post-translational modification, or transcription factor synthesis. In the latter case, RNA-binding proteins such as Hfq, CsrA/RsmA, and components of the RNA degradosome alter mRNA stability and/or the rate of translation initiation to control transcription factor synthesis. Here we summarize post-transcriptional mechanisms that contribute to the exquisite regulation of T3SS gene expression.
III型分泌系统(T3SS)是许多革兰氏阴性植物和动物病原体的主要抗宿主防御机制。T3SS的产生受到宿主相关信号的严格控制和激活。虽然转录反应是激活级联反应的重要组成部分,但最近的研究发现了多种转录后机制,这些机制也有助于T3SS的产生。转录后控制的靶点通常是促进T3SS基因表达的AraC/XylS转录因子。转录后调控的常见机制包括通过蛋白质配体、小分子或翻译后修饰直接控制AraC/XylS转录因子的活性,或转录因子合成。在后一种情况下,诸如Hfq、CsrA/RsmA等RNA结合蛋白以及RNA降解体的成分会改变mRNA的稳定性和/或翻译起始速率,以控制转录因子的合成。在此,我们总结了有助于T3SS基因表达精确调控的转录后机制。