Dong Qian, Fang Mingxu, Roychowdhury Sugata, Bauer Carl E
Molecular and Cellular Biochemistry Department, Indiana University, Bloomington, IN, 47405, USA.
Present address: Owensboro Cancer Research Program, University of Louisville James Graham Brown Cancer Center, Owensboro, KY, 42303, USA.
BMC Genomics. 2015 Dec 16;16:1066. doi: 10.1186/s12864-015-2248-z.
Several Gram-negative species undergo development leading to the formation of metabolically dormant desiccation resistant cysts. Recent analysis of cyst development has revealed that ~20 % of the Rhodospirillum centenum transcriptome undergo temporal changes in expression as cells transition from vegetative to cyst forms. It has also been established that one trigger for cyst formation is the synthesis of the signaling nucleotide 3', 5'- cyclic guanosine monophosphate (cGMP) that is sensed by a homolog of the catabolite repressor protein called CgrA. CgrA in the presence of cGMP initiate a cascade of gene expression leading to the development of cysts.
In this study, we have used RNA-seq and chromatin immunoprecipitation (ChIP-Seq) techniques to define the CgrA-cGMP regulon. Our results indicate that disruption of CgrA leads to altered expression of 258 genes, 131 of which have been previously reported to be involved in cyst development. ChIP-seq analysis combined with transcriptome data also demonstrates that CgrA directly regulates the expression of numerous sigma factors and transcription factors several of which are known to be involved in cyst cell development.
This analysis reveals the presence of CgrA binding sites upstream of many developmentally regulated genes including many transcription factors and signal transduction components. CgrA thus functions as master controller of the cyst development by initiating a hierarchal cascade of downstream transcription factors that induces temporal expression of encystment genes.
几种革兰氏阴性菌会经历发育过程,最终形成代谢休眠且抗干燥的孢囊。最近对孢囊发育的分析表明,当细胞从营养态转变为孢囊态时,约20%的深红红螺菌转录组在表达上会发生时间变化。还已确定,孢囊形成的一个触发因素是信号核苷酸3',5'-环鸟苷单磷酸(cGMP)的合成,它由一种名为CgrA的分解代谢物阻遏蛋白同源物感知。在cGMP存在的情况下,CgrA启动一系列基因表达,导致孢囊发育。
在本研究中,我们使用RNA测序(RNA-seq)和染色质免疫沉淀(ChIP-Seq)技术来定义CgrA-cGMP调控子。我们的结果表明,CgrA的破坏导致258个基因的表达改变,其中131个基因先前已报道参与孢囊发育。ChIP-seq分析与转录组数据相结合还表明,CgrA直接调控众多σ因子和转录因子的表达,其中一些已知参与孢囊细胞发育。
该分析揭示了许多发育调控基因上游存在CgrA结合位点,包括许多转录因子和信号转导成分。因此,CgrA通过启动下游转录因子的层级级联反应来诱导包囊化基因的时间表达,从而作为孢囊发育的主控因子发挥作用。