Guimerà Roger, Nunes Amaral Luís A
NICO and Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Nature. 2005 Feb 24;433(7028):895-900. doi: 10.1038/nature03288.
High-throughput techniques are leading to an explosive growth in the size of biological databases and creating the opportunity to revolutionize our understanding of life and disease. Interpretation of these data remains, however, a major scientific challenge. Here, we propose a methodology that enables us to extract and display information contained in complex networks. Specifically, we demonstrate that we can find functional modules in complex networks, and classify nodes into universal roles according to their pattern of intra- and inter-module connections. The method thus yields a 'cartographic representation' of complex networks. Metabolic networks are among the most challenging biological networks and, arguably, the ones with most potential for immediate applicability. We use our method to analyse the metabolic networks of twelve organisms from three different superkingdoms. We find that, typically, 80% of the nodes are only connected to other nodes within their respective modules, and that nodes with different roles are affected by different evolutionary constraints and pressures. Remarkably, we find that metabolites that participate in only a few reactions but that connect different modules are more conserved than hubs whose links are mostly within a single module.
高通量技术正促使生物数据库规模呈爆发式增长,并为彻底改变我们对生命和疾病的理解创造了机会。然而,对这些数据的解读仍然是一项重大的科学挑战。在此,我们提出一种方法,使我们能够提取并展示复杂网络中包含的信息。具体而言,我们证明能够在复杂网络中找到功能模块,并根据节点在模块内和模块间的连接模式将其分类为通用角色。该方法由此产生复杂网络的“地图表示”。代谢网络是最具挑战性的生物网络之一,可以说也是最具直接应用潜力的网络。我们使用我们的方法分析来自三个不同超界的十二种生物的代谢网络。我们发现,通常80%的节点仅与各自模块内的其他节点相连,并且具有不同角色的节点受到不同的进化约束和压力影响。值得注意的是,我们发现仅参与少数反应但连接不同模块的代谢物比那些连接大多在单个模块内的中心节点更保守。