Martin Alberto J, Contreras-Riquelme Sebastián, Dominguez Calixto, Perez-Acle Tomas
Computational Biology Laboratory (DLab), Fundacion Ciencia y Vida, Santiago, Chile; Centro Interdisciplinario de Neurociencia de Valparaíso, Valparaiso, Chile.
Computational Biology Laboratory (DLab), Fundacion Ciencia y Vida, Santiago, Chile; Facultad de Ciencias Biologicas, Universidad Andres Bello, Santiago, Chile.
PeerJ. 2017 Feb 28;5:e3052. doi: 10.7717/peerj.3052. eCollection 2017.
One of the main challenges of the post-genomic era is the understanding of how gene expression is controlled. Changes in gene expression lay behind diverse biological phenomena such as development, disease and the adaptation to different environmental conditions. Despite the availability of well-established methods to identify these changes, tools to discern how gene regulation is orchestrated are still required. The regulation of gene expression is usually depicted as a Gene Regulatory Network (GRN) where changes in the network structure (i.e., network topology) represent adjustments of gene regulation. Like other networks, GRNs are composed of basic building blocks; small induced subgraphs called graphlets. Here we present , a novel method that using Graphlet Based Metrics (GBMs) identifies topological variations between different states of a GRN. Under our approach, different states of a GRN are analyzed to determine the types of graphlet formed by all triplets of nodes in the network. Subsequently, graphlets occurring in a state of the network are compared to those formed by the same three nodes in another version of the network. Once the comparisons are performed, applies metrics from binary classification problems calculated on the existence and absence of graphlets to assess the topological similarity between both network states. Experiments performed on randomized networks demonstrate that GBMs are more sensitive to topological variation than the same metrics calculated on single edges. Additional comparisons with other common metrics demonstrate that our GBMs are capable to identify nodes whose local topology changes between different states of the network. Notably, due to the explicit use of graphlets, captures topological variations that are disregarded by other approaches. is freely available as an online web server at http://dlab.cl/loto.
后基因组时代的主要挑战之一是理解基因表达是如何被调控的。基因表达的变化是多种生物学现象的基础,如发育、疾病以及对不同环境条件的适应。尽管已有成熟的方法来识别这些变化,但仍需要工具来辨别基因调控是如何协调的。基因表达的调控通常被描绘为一个基因调控网络(GRN),其中网络结构的变化(即网络拓扑)代表基因调控的调整。与其他网络一样,GRN由基本构建块组成;称为图元的小诱导子图。在这里,我们提出了一种新方法,即使用基于图元的度量(GBM)来识别GRN不同状态之间的拓扑变化。在我们的方法中,分析GRN的不同状态以确定网络中所有节点三元组形成的图元类型。随后,将网络一种状态中出现的图元与网络另一个版本中相同三个节点形成的图元进行比较。一旦完成比较,就应用基于图元存在与否计算的二元分类问题的度量来评估两个网络状态之间的拓扑相似性。在随机网络上进行的实验表明,GBM对拓扑变化比基于单边计算的相同度量更敏感。与其他常用度量的进一步比较表明,我们的GBM能够识别其局部拓扑在网络不同状态之间发生变化的节点。值得注意的是,由于明确使用了图元,该方法捕捉到了其他方法忽略的拓扑变化。该方法可作为在线网络服务器免费获取,网址为http://dlab.cl/loto。