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Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes

机译:从整个基因组的系统发育统计分析得出的蛋白质网络的装配规则

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BackgroundWe report an analysis of a protein network of functionally linked proteins, identified from a phylogenetic statistical analysis of complete eukaryotic genomes. Phylogenetic methods identify pairs of proteins that co-evolve on a phylogenetic tree, and have been shown to have a high probability of correctly identifying known functional links.ResultsThe eukaryotic correlated evolution network we derive displays the familiar power law scaling of connectivity. We introduce the use of explicit phylogenetic methods to reconstruct the ancestral presence or absence of proteins at the interior nodes of a phylogeny of eukaryote species. We find that the connectivity distribution of proteins at the point they arise on the tree and join the network follows a power law, as does the connectivity distribution of proteins at the time they are lost from the network. Proteins resident in the network acquire connections over time, but we find no evidence that 'preferential attachment' – the phenomenon of newly acquired connections in the network being more likely to be made to proteins with large numbers of connections – influences the network structure. We derive a 'variable rate of attachment' model in which proteins vary in their propensity to form network interactions independently of how many connections they have or of the total number of connections in the network, and show how this model can produce apparent power-law scaling without preferential attachment.ConclusionA few simple rules can explain the topological structure and evolutionary changes to protein-interaction networks: most change is concentrated in satellite proteins of low connectivity and small phenotypic effect, and proteins differ in their propensity to form attachments. Given these rules of assembly, power law scaled networks naturally emerge from simple principles of selection, yielding protein interaction networks that retain a high-degree of robustness on short time scales and evolvability on longer evolutionary time scales.
机译:背景我们报告了功能连接蛋白的蛋白质网络的分析,该蛋白网络是根据完整的真核基因组的系统发育统计分析确定的。系统发育方法可识别在进化树上共同进化的蛋白质对,并已被证明具有正确识别已知功能链接的高可能性。结果我们得到的真核相关进化网络显示出熟悉的幂律连通性尺度。我们介绍了使用显式系统发育方法来重建真核生物种系内部节点中蛋白质的祖先存在或不存在。我们发现蛋白质在树上出现并连接到网络时的连接分布遵循幂律,蛋白质从网络中丢失时的连接分布也遵循幂律。驻留在网络中的蛋白质会随着时间的推移获得连接,但我们没有发现证据表明“优先连接”(网络中新获得的连接更可能与具有大量连接的蛋白质发生连接的现象)会影响网络结构。我们推导了一个“可变附着速率”模型,其中蛋白质形成网络相互作用的倾向与蛋白质具有多少连接或网络中的连接总数无关,并且表明该模型如何产生明显的幂律。结论没有几个简单的规则就可以解释蛋白质相互作用网络的拓扑结构和进化变化:大多数变化集中在低连接性和小表型效应的卫星蛋白质上,蛋白质形成附件的倾向也不同。给定这些组装规则,幂律定标网络自然会从简单的选择原理中出现,从而产生蛋白质相互作用网络,在较短的时间尺度上保持高度的鲁棒性,而在较长的进化时间尺度上保持可进化性。

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