Li Jie, Overall Christopher C, Johnson Rudd C, Jones Marcus B, McDermott Jason E, Heffron Fred, Adkins Joshua N, Cambronne Eric D
Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, United States of America.
Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States of America.
PLoS One. 2015 Sep 21;10(9):e0138466. doi: 10.1371/journal.pone.0138466. eCollection 2015.
The alternative sigma factor σE functions to maintain bacterial homeostasis and membrane integrity in response to extracytoplasmic stress by regulating thousands of genes both directly and indirectly. The transcriptional regulatory network governed by σE in Salmonella and E. coli has been examined using microarray, however a genome-wide analysis of σE-binding sites in Salmonella has not yet been reported. We infected macrophages with Salmonella Typhimurium over a select time course. Using chromatin immunoprecipitation followed by high-throughput DNA sequencing (ChIP-seq), 31 σE-binding sites were identified. Seventeen sites were new, which included outer membrane proteins, a quorum-sensing protein, a cell division factor, and a signal transduction modulator. The consensus sequence identified for σE in vivo binding was similar to the one previously reported, except for a conserved G and A between the -35 and -10 regions. One third of the σE-binding sites did not contain the consensus sequence, suggesting there may be alternative mechanisms by which σE modulates transcription. By dissecting direct and indirect modes of σE-mediated regulation, we found that σE activates gene expression through recognition of both canonical and reversed consensus sequence. New σE regulated genes (greA, luxS, ompA and ompX) are shown to be involved in heat shock and oxidative stress responses.
替代σ因子σE通过直接和间接调控数千个基因,在应对胞外应激时维持细菌内稳态和膜完整性。已使用微阵列研究了沙门氏菌和大肠杆菌中由σE控制的转录调控网络,然而尚未有关于沙门氏菌中σE结合位点的全基因组分析报道。我们在选定的时间进程中用鼠伤寒沙门氏菌感染巨噬细胞。通过染色质免疫沉淀结合高通量DNA测序(ChIP-seq),鉴定出31个σE结合位点。其中17个位点是新发现的,包括外膜蛋白、群体感应蛋白、细胞分裂因子和信号转导调节剂。体内σE结合鉴定出的共有序列与先前报道的相似,只是在-35和-10区域之间有一个保守的G和A。三分之一的σE结合位点不包含共有序列,这表明σE可能存在调节转录的其他机制。通过剖析σE介导调控的直接和间接模式,我们发现σE通过识别典型和反向共有序列来激活基因表达。新发现的受σE调控的基因(greA、luxS、ompA和ompX)显示参与热休克和氧化应激反应。