Borotkanics Robert, Lehmann Harold
Department of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA,
Arch Toxicol. 2015 Apr;89(4):489-99. doi: 10.1007/s00204-014-1274-y. Epub 2014 May 22.
Cellular molecules interact in complex ways, giving rise to a cell's functional outcomes. Conscientious efforts have been made in recent years to better characterize these patterns of interactions. It has been learned that many of these interactions can be represented abstractly as a network and within a network there in many instances are network motifs. Network motifs are subgraphs that are statistically overrepresented within networks. To date, specific network motifs have been experimentally identified across various species and also within specific, intracellular networks; however, motifs that recur across species and major network types have not been systematically characterized. We reason that recurring network motifs could potentially have important implications and applications for toxicology and, in particular, toxicity testing. Therefore, the goal of this study was to determine the set of intracellular, network motifs found to recur across species of both gene regulatory and protein-protein interaction networks. We report the recurrence of 13 intracellular, network motifs across species. Ten recurring motifs were found across both protein-protein interaction networks and gene regulatory networks. The significant pair motif was found to recur only in gene regulatory networks. The diamond and one-way cycle reversible step motifs were found to recur only in protein-protein interaction networks. This study is the first formal review of recurring, intracellular network motifs across species. Within toxicology, combining our understanding of recurring motifs with mechanism and mode of action knowledge could result in more robust and efficient toxicity testing models. We are sure that our results will support research in applying network motifs to toxicity testing.
细胞分子以复杂的方式相互作用,从而产生细胞的功能结果。近年来,人们一直在认真努力,以更好地描述这些相互作用模式。现已了解到,其中许多相互作用可以抽象地表示为一个网络,并且在一个网络中,在许多情况下都存在网络基序。网络基序是在网络中统计上过度出现的子图。迄今为止,已经在各种物种以及特定的细胞内网络中通过实验确定了特定的网络基序;然而,跨物种和主要网络类型反复出现的基序尚未得到系统的表征。我们推断,反复出现的网络基序可能对毒理学,特别是毒性测试具有重要意义和应用价值。因此,本研究的目的是确定在基因调控网络和蛋白质-蛋白质相互作用网络的物种中反复出现的细胞内网络基序集。我们报告了13种细胞内网络基序在物种间的反复出现情况。在蛋白质-蛋白质相互作用网络和基因调控网络中都发现了10种反复出现的基序。发现显著对基序仅在基因调控网络中反复出现。发现菱形和单向循环可逆步骤基序仅在蛋白质-蛋白质相互作用网络中反复出现。本研究是对跨物种反复出现的细胞内网络基序的首次正式综述。在毒理学领域,将我们对反复出现的基序的理解与作用机制和作用方式知识相结合,可能会产生更强大、更有效的毒性测试模型。我们确信我们的结果将支持将网络基序应用于毒性测试的研究。