Vella Danila, Zoppis Italo, Mauri Giancarlo, Mauri Pierluigi, Di Silvestre Dario
Institute for Biomedical Technologies - National Research Council (ITB-CNR), 93 Fratelli Cervi, Segrate, Milan, Italy.
Department of Computer Science, Systems and Communication DiSCo, University of Milano-Bicocca, 336 Viale Sarca, Milan, Italy.
EURASIP J Bioinform Syst Biol. 2017 Dec;2017(1):6. doi: 10.1186/s13637-017-0059-z. Epub 2017 Mar 20.
The reductionist approach of dissecting biological systems into their constituents has been successful in the first stage of the molecular biology to elucidate the chemical basis of several biological processes. This knowledge helped biologists to understand the complexity of the biological systems evidencing that most biological functions do not arise from individual molecules; thus, realizing that the emergent properties of the biological systems cannot be explained or be predicted by investigating individual molecules without taking into consideration their relations. Thanks to the improvement of the current -omics technologies and the increasing understanding of the molecular relationships, even more studies are evaluating the biological systems through approaches based on graph theory. Genomic and proteomic data are often combined with protein-protein interaction (PPI) networks whose structure is routinely analyzed by algorithms and tools to characterize hubs/bottlenecks and topological, functional, and disease modules. On the other hand, co-expression networks represent a complementary procedure that give the opportunity to evaluate at system level including organisms that lack information on PPIs. Based on these premises, we introduce the reader to the PPI and to the co-expression networks, including aspects of reconstruction and analysis. In particular, the new idea to evaluate large-scale proteomic data by means of co-expression networks will be discussed presenting some examples of application. Their use to infer biological knowledge will be shown, and a special attention will be devoted to the topological and module analysis.
将生物系统分解为其组成部分的还原论方法在分子生物学的第一阶段取得了成功,阐明了几种生物过程的化学基础。这些知识帮助生物学家理解了生物系统的复杂性,证明大多数生物功能并非源于单个分子;因此,人们认识到,如果不考虑分子之间的关系,仅研究单个分子是无法解释或预测生物系统的涌现特性的。由于当前组学技术的改进以及对分子关系的日益了解,越来越多的研究开始通过基于图论的方法来评估生物系统。基因组和蛋白质组数据通常与蛋白质-蛋白质相互作用(PPI)网络相结合,其结构通常通过算法和工具进行分析,以表征枢纽/瓶颈以及拓扑、功能和疾病模块。另一方面,共表达网络是一种补充方法,它提供了在系统水平上进行评估的机会,包括那些缺乏PPI信息的生物体。基于这些前提,我们向读者介绍PPI和共表达网络,包括重建和分析方面。特别是,将讨论通过共表达网络评估大规模蛋白质组数据的新想法,并展示一些应用实例。将展示它们在推断生物学知识方面的用途,并将特别关注拓扑和模块分析。