Department of Biology, University of Alabama at Birmingham, Birmingham, USA.
Department of Computer & Information Sciences, University of Alabama at Birmingham, Birmingham, USA.
Sci Rep. 2017 Aug 10;7(1):7849. doi: 10.1038/s41598-017-08073-z.
The universal nature of networks' structural and physical properties across diverse systems offers a better prospect to elucidate the interplay between a system and its environment. In the last decade, several large-scale transcriptome and interactome studies were conducted to understand the complex and dynamic nature of interactions between Arabidopsis and its bacterial pathogen, Pseudomonas syringae pv. tomato DC3000. We took advantage of these publicly available datasets and performed "-omics"-based integrative, and network topology analyses to decipher the transcriptional and protein-protein interaction activities of effector targets. We demonstrated that effector targets exhibit shorter distance to differentially expressed genes (DEGs) and possess increased information centrality. Intriguingly, effector targets are differentially expressed in a sequential manner and make for 1% of the total DEGs at any time point of infection with virulent or defense-inducing DC3000 strains. We revealed that DC3000 significantly alters the expression levels of 71% effector targets and their downstream physical interacting proteins in Arabidopsis interactome. Our integrative "-omics"--based analyses identified dynamic complexes associated with MTI and disease susceptibility. Finally, we discovered five novel plant defense players using a systems biology-fueled top-to-bottom approach and demonstrated immune-related functions for them, further validating the power and resolution of our network analyses.
网络的结构和物理性质在不同系统中的普遍性为阐明系统与其环境之间的相互作用提供了更好的前景。在过去的十年中,进行了几项大规模的转录组和互作组研究,以了解拟南芥与其细菌病原体丁香假单胞菌 pv.番茄 DC3000 之间复杂和动态的相互作用性质。我们利用这些公开可用的数据集,进行了基于“组学”的综合和网络拓扑分析,以破译效应靶标的转录和蛋白-蛋白相互作用活性。我们证明了效应靶标与差异表达基因 (DEGs) 的距离更短,并且具有增加的信息中心性。有趣的是,效应靶标以顺序方式差异表达,并且在感染强毒力或诱导防御的 DC3000 菌株的任何时间点,占总 DEGs 的 1%。我们揭示了 DC3000 显著改变了拟南芥互作组中 71%的效应靶标及其下游物理相互作用蛋白的表达水平。我们的基于综合“组学”的分析确定了与 MTI 和疾病易感性相关的动态复合物。最后,我们使用基于系统生物学的自上而下的方法发现了五个新的植物防御参与者,并证明了它们的免疫相关功能,进一步验证了我们的网络分析的力量和分辨率。