Sowa Steven W, Gelderman Grant, Leistra Abigail N, Buvanendiran Aishwarya, Lipp Sarah, Pitaktong Areen, Vakulskas Christopher A, Romeo Tony, Baldea Michael, Contreras Lydia M
Microbiology Graduate Program, University of Texas at Austin, 100 E. 24th Street Stop A6500, Austin, TX 78712, USA.
McKetta Department of Chemical Engineering, University of Texas at Austin, 200 E. Dean Keeton Street Stop C0400, Austin, TX 78712, USA.
Nucleic Acids Res. 2017 Feb 28;45(4):1673-1686. doi: 10.1093/nar/gkx048.
Multi-target regulators represent a largely untapped area for metabolic engineering and anti-bacterial development. These regulators are complex to characterize because they often act at multiple levels, affecting proteins, transcripts and metabolites. Therefore, single omics experiments cannot profile their underlying targets and mechanisms. In this work, we used an Integrative FourD omics approach (INFO) that consists of collecting and analyzing systems data throughout multiple time points, using multiple genetic backgrounds, and multiple omics approaches (transcriptomics, proteomics and high throughput sequencing crosslinking immunoprecipitation) to evaluate simultaneous changes in gene expression after imposing an environmental stress that accentuates the regulatory features of a network. Using this approach, we profiled the targets and potential regulatory mechanisms of a global regulatory system, the well-studied carbon storage regulatory (Csr) system of Escherichia coli, which is widespread among bacteria. Using 126 sets of proteomics and transcriptomics data, we identified 136 potential direct CsrA targets, including 50 novel ones, categorized their behaviors into distinct regulatory patterns, and performed in vivo fluorescence-based follow up experiments. The results of this work validate 17 novel mRNAs as authentic direct CsrA targets and demonstrate a generalizable strategy to integrate multiple lines of omics data to identify a core pool of regulator targets.
多靶点调节因子在代谢工程和抗菌药物研发方面很大程度上仍是未开发领域。这些调节因子的特性很难描述,因为它们常常在多个层面发挥作用,影响蛋白质、转录本和代谢物。因此,单一的组学实验无法描绘其潜在靶点和作用机制。在这项研究中,我们采用了一种综合四维组学方法(INFO),该方法包括在多个时间点、使用多种遗传背景以及多种组学方法(转录组学、蛋白质组学和高通量测序交联免疫沉淀)收集和分析系统数据,以评估在施加一种能突出网络调节特征的环境应激后基因表达的同步变化。利用这种方法,我们描绘了一个全局调节系统——在细菌中广泛存在且研究充分的大肠杆菌碳储存调节(Csr)系统——的靶点和潜在调节机制。通过126组蛋白质组学和转录组学数据,我们鉴定出136个潜在的CsrA直接靶点,包括50个新靶点,将它们的行为分类为不同的调节模式,并进行了基于体内荧光的后续实验。这项研究的结果验证了17个新的mRNA是真正的CsrA直接靶点,并展示了一种整合多组学数据以识别调节因子靶点核心库的通用策略。