Gabr Haitham, Kahveci Tamer
BMC Bioinformatics. 2015;16 Suppl 17(Suppl 17):S6. doi: 10.1186/1471-2105-16-S17-S6. Epub 2015 Dec 7.
Studying biological networks is of extreme importance in understanding cellular functions. These networks model interactions between molecules in each cell. A large volume of research has been done to uncover different characteristics of biological networks, such as large-scale organization, node centrality and network robustness. Nevertheless, the vast majority of research done in this area assume that biological networks have deterministic topologies. Biological interactions are however probabilistic events that may or may not appear at different cells or even in the same cell at different times.
In this paper, we present novel methods for characterizing probabilistic signaling networks. Our methods do this by computing the probability that a signal propagates successfully from receptor to reporter genes through interactions in the network. We characterize such networks with respect to (i) centrality of individual nodes, (ii) stability of the entire network, and (iii) important functions served by the network. We use these methods to characterize major H. sapiens signaling networks including Wnt, ErbB and MAPK.
研究生物网络对于理解细胞功能极为重要。这些网络对每个细胞中分子间的相互作用进行建模。为揭示生物网络的不同特征,如大规模组织、节点中心性和网络鲁棒性,已经开展了大量研究。然而,该领域的绝大多数研究都假定生物网络具有确定性拓扑结构。然而,生物相互作用是概率性事件,在不同细胞甚至同一细胞的不同时间可能出现也可能不出现。
在本文中,我们提出了表征概率信号网络的新方法。我们的方法通过计算信号在网络中通过相互作用从受体成功传播到报告基因的概率来实现这一点。我们从以下几个方面对这类网络进行表征:(i)单个节点的中心性,(ii)整个网络的稳定性,以及(iii)网络所发挥的重要功能。我们使用这些方法来表征包括Wnt、ErbB和MAPK在内的主要人类信号网络。