论文标题
信号指标分析细菌多OMIC网络中的振荡模式
Signal metrics analysis of oscillatory patterns in bacterial multi-omic networks
论文作者
论文摘要
动机:通过分析生物分子振荡及其相互作用,系统生物学的一个分支集中在对潜在调节网络的深刻理解上。合成生物学利用基因或/和蛋白质调节网络来设计振荡网络,以产生有用的化合物。因此,在不同级别的应用和不同目的的情况下,生物分子振荡的研究可能会导致有关活细胞所基于的机制的不同线索。众所周知,网络级相互作用涉及多种类型的生物分子以及以多种OMIC水平运行的生物过程。将网络/途径级信息与遗传信息相结合,可以描述良好或未知的细菌机制和有机体特定的动力学。结果:网络多OMIC集成导致发现了有趣的振荡信号。遵循信号处理和通信工程中使用的方法,引入了一种新方法,以识别和量化信号的多摩尼克振荡程度。新的信号指标旨在允许进一步的生物技术解释,并提供有关途径及其调节回路的振荡性质的重要线索。我们设计用于分析多族信号的算法对在11种不同的细菌上进行了测试和验证,该算法因通过不同的实验条件在网络级别扰动的数千个多摩变信号。有关基因,密码子使用,基因表达和蛋白质分子量的顺序的信息,以三种不同的功能水平整合。振荡显示了有趣的证据,表明网络级多摩尼克信号与分类单元同步对扰动和进化关系的响应。
Motivation: One of the branches of Systems Biology is focused on a deep understanding of underlying regulatory networks through the analysis of the biomolecules oscillations and their interplay. Synthetic Biology exploits gene or/and protein regulatory networks towards the design of oscillatory networks for producing useful compounds. Therefore, at different levels of application and for different purposes, the study of biomolecular oscillations can lead to different clues about the mechanisms underlying living cells. It is known that network-level interactions involve more than one type of biomolecule as well as biological processes operating at multiple omic levels. Combining network/pathway-level information with genetic information it is possible to describe well-understood or unknown bacterial mechanisms and organism-specific dynamics. Results: Network multi-omic integration has led to the discovery of interesting oscillatory signals. Following the methodologies used in signal processing and communication engineering, a new methodology is introduced to identify and quantify the extent of the multi-omic oscillations of the signal. New signal metrics are designed to allow further biotechnological explanations and provide important clues about the oscillatory nature of the pathways and their regulatory circuits. Our algorithms designed for the analysis of multi-omic signals are tested and validated on 11 different bacteria for thousands of multi-omic signals perturbed at the network level by different experimental conditions. Information on the order of genes, codon usage, gene expression, and protein molecular weight is integrated at three different functional levels. Oscillations show interesting evidence that network-level multi-omic signals present a synchronized response to perturbations and evolutionary relations along with taxa.