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Robustness and Evolvability of the Human Signaling Network

机译:人类信号网络的鲁棒性和可扩展性

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Biological systems are known to be both robust and evolvable to internal and external perturbations, but what causes these apparently contradictory properties? We used Boolean network modeling and attractor landscape analysis to investigate the evolvability and robustness of the human signaling network. Our results show that the human signaling network can be divided into an evolvable core where perturbations change the attractor landscape in state space, and a robust neighbor where perturbations have no effect on the attractor landscape. Using chemical inhibition and overexpression of nodes, we validated that perturbations affect the evolvable core more strongly than the robust neighbor. We also found that the evolvable core has a distinct network structure, which is enriched in feedback loops, and features a higher degree of scale-freeness and longer path lengths connecting the nodes. In addition, the genes with high evolvability scores are associated with evolvability-related properties such as rapid evolvability, low species broadness, and immunity whereas the genes with high robustness scores are associated with robustness-related properties such as slow evolvability, high species broadness, and oncogenes. Intriguingly, US Food and Drug Administration-approved drug targets have high evolvability scores whereas experimental drug targets have high robustness scores.
机译:众所周知,生物系统既健壮又可发展为内部和外部的扰动,但是是什么原因导致这些明显矛盾的特性呢?我们使用布尔网络建模和吸引子景观分析来研究人类信号网络的发展性和鲁棒性。我们的研究结果表明,人类信号网络可分为扰动改变状态空间中吸引子景观的可演化核心和扰动对吸引子景观无影响的强大邻居。使用化学抑制和节点的过表达,我们验证了扰动对可演化核心的影响比对健壮邻居的影响更大。我们还发现,可演化的核心具有独特的网络结构,该网络结构丰富了反馈回路,并且具有更高的无标度和连接节点的路径长度更长的特征。此外,具有高进化评分的基因与进化相关的特性(例如快速进化,低物种广度和免疫力)相关,而具有高鲁棒性评分的基因与与鲁棒性相关的特性(例如缓慢进化,高物种广度,和致癌基因。有趣的是,美国食品药品监督管理局批准的药物靶标具有较高的可进化性评分,而实验药物靶标具有较高的鲁棒性评分。

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