Ta Hung Xuan, Yoon Chang No, Holm Liisa, Han Seung Kee
Institute of Biotechnology, PO Box 56, 00014 University of Helsinki, Finland.
BMC Syst Biol. 2010 May 26;4:70. doi: 10.1186/1752-0509-4-70.
Biological networks, such as protein-protein interactions, metabolic, signalling, transcription-regulatory networks and neural synapses, are representations of large-scale dynamic systems. The relationship between the network structure and functions remains one of the central problems in current multidisciplinary research. Significant progress has been made toward understanding the implication of topological features for the network dynamics and functions, especially in biological networks. Given observations of a network system's behaviours or measurements of its functional dynamics, what can we conclude of the details of physical connectivity of the underlying structure?
We modelled the network system by employing a scale-free network of coupled phase oscillators. Pairwise phase coherence (PPC) was calculated for all the pairs of oscillators to present functional dynamics induced by the system. At the regime of global incoherence, we observed a Significant pairwise synchronization only between two nodes that are physically connected. Right after the onset of global synchronization, disconnected nodes begin to oscillate in a correlated fashion and the PPC of two nodes, either connected or disconnected, depends on their degrees.Based on the observation of PPCs, we built a weighted network of synchronization (WNS), an all-to-all functionally connected network where each link is weighted by the PPC of two oscillators at the ends of the link. In the regime of strong coupling, we observed a Significant similarity in the organization of WNSs induced by systems sharing the same substrate network but different configurations of initial phases and intrinsic frequencies of oscillators.We reconstruct physical network from the WNS by choosing the links whose weights are higher than a given threshold. We observed an optimal reconstruction just before the onset of global synchronization.Finally, we correlated the topology of the background network to the observed change of the functional activities in the system.
The results presented in this study indicate a strong relationship between the structure and dynamics of complex network systems. As coupling strength increases, synchronization emerges among hub nodes and recruits small-degree nodes. The results show that the onset of global synchronization in the system hinders the reconstruction of an underlying complex structure. Our analysis helps to clarify how the synchronization is achieved in systems of different network topologies.
生物网络,如蛋白质 - 蛋白质相互作用、代谢、信号传导、转录调控网络和神经突触,是大规模动态系统的表现形式。网络结构与功能之间的关系仍然是当前多学科研究的核心问题之一。在理解拓扑特征对网络动态和功能的影响方面已经取得了重大进展,特别是在生物网络中。鉴于对网络系统行为的观察或其功能动态的测量,我们能对潜在结构的物理连通性细节得出什么结论呢?
我们通过使用耦合相位振荡器的无标度网络对网络系统进行建模。计算所有振荡器对之间的成对相位相干性(PPC),以呈现系统诱导的功能动态。在全局非相干状态下,我们仅在物理上相连的两个节点之间观察到显著的成对同步。在全局同步开始后不久,不相连的节点开始以相关方式振荡,并且两个节点(无论相连与否)的PPC取决于它们的度数。基于对PPC的观察,我们构建了一个同步加权网络(WNS),这是一个全对全功能连接的网络,其中每个链接由链接两端两个振荡器的PPC加权。在强耦合状态下,我们观察到由共享相同底物网络但振荡器的初始相位和固有频率配置不同的系统诱导的WNS在组织上有显著相似性。我们通过选择权重高于给定阈值的链接从WNS重建物理网络。我们在全局同步开始前观察到了最佳重建。最后,我们将背景网络的拓扑结构与系统中观察到的功能活动变化相关联。
本研究中呈现的结果表明复杂网络系统的结构与动态之间存在密切关系。随着耦合强度增加,枢纽节点之间出现同步并吸引小度数节点。结果表明系统中全局同步的开始阻碍了潜在复杂结构的重建。我们的分析有助于阐明在不同网络拓扑结构的系统中如何实现同步。