National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20892
Proc Natl Acad Sci U S A. 2014 May 13;111(19):7156-60. doi: 10.1073/pnas.1311231111. Epub 2014 Apr 28.
Recently, the focus of network research shifted to network controllability, prompting us to determine proteins that are important for the control of the underlying interaction webs. In particular, we determined minimum dominating sets of proteins (MDSets) in human and yeast protein interaction networks. Such groups of proteins were defined as optimized subsets where each non-MDSet protein can be reached by an interaction from an MDSet protein. Notably, we found that MDSet proteins were enriched with essential, cancer-related, and virus-targeted genes. Their central position allowed MDSet proteins to connect protein complexes and to have a higher impact on network resilience than hub proteins. As for their involvement in regulatory functions, MDSet proteins were enriched with transcription factors and protein kinases and were significantly involved in bottleneck interactions, regulatory links, phosphorylation events, and genetic interactions.
最近,网络研究的焦点转移到了网络可控性上,这促使我们确定对于底层相互作用网络的控制很重要的蛋白质。特别是,我们确定了人类和酵母蛋白质相互作用网络中的最小支配集(MDSets)。这些蛋白质组被定义为优化子集,其中每个非 MDSet 蛋白质都可以通过 MDSet 蛋白质的相互作用来达到。值得注意的是,我们发现 MDSet 蛋白质富含必需的、与癌症相关的和针对病毒的基因。它们的中心位置使 MDSet 蛋白质能够连接蛋白质复合物,并对网络弹性产生比枢纽蛋白质更高的影响。至于它们在调节功能中的参与,MDSet 蛋白质富含转录因子和蛋白激酶,并且它们显著参与瓶颈相互作用、调节链接、磷酸化事件和遗传相互作用。