Liang Han, Li Wen-Hsiung
Department of Ecology and Evolution, University of Chicago, IL 60637, USA.
RNA. 2007 Sep;13(9):1402-8. doi: 10.1261/rna.634607. Epub 2007 Jul 24.
Since the functional state of a protein-protein interaction network depends on gene expression, a fundamental question is what relationships exist between protein interaction network and gene regulation. In particular, microRNAs have recently emerged as a major class of post-transcriptional regulators that influences a large proportion of genes in higher eukaryotes. Here we show that protein connectivity in the human protein-protein interaction network is positively correlated with the number of microRNA target-site types in the 3' untranslated regions of the gene encoding the protein and that interacting proteins tend to share more microRNA target-site types than random pairs. Moreover, our results demonstrate that microRNA targeting propensity for genes in different biological processes can be largely explained by their protein connectivity. Finally, we show that for hub proteins, microRNA regulation complexity is negatively correlated with clustering coefficient, suggesting that microRNA regulation is more important to inter-modular hubs than to intramodular ones. Taken together, our study provides the first evidence for global correlation between microRNA repression and protein-protein interactions.
由于蛋白质-蛋白质相互作用网络的功能状态取决于基因表达,一个基本问题是蛋白质相互作用网络与基因调控之间存在何种关系。特别是,微小RNA最近已成为一类主要的转录后调节因子,影响高等真核生物中很大一部分基因。我们在此表明,人类蛋白质-蛋白质相互作用网络中的蛋白质连接性与编码该蛋白质的基因的3'非翻译区中微小RNA靶位点类型的数量呈正相关,并且相互作用的蛋白质往往比随机配对的蛋白质共享更多的微小RNA靶位点类型。此外,我们的结果表明,不同生物学过程中基因的微小RNA靶向倾向在很大程度上可以由它们的蛋白质连接性来解释。最后,我们表明,对于枢纽蛋白,微小RNA调控复杂性与聚类系数呈负相关,这表明微小RNA调控对模块间枢纽比对模块内枢纽更重要。综上所述,我们的研究为微小RNA抑制与蛋白质-蛋白质相互作用之间的全局相关性提供了首个证据。