Ma Hong-Wu, Kumar Bharani, Ditges Uta, Gunzer Florian, Buer Jan, Zeng An-Ping
Department of Genome Analysis and Department of Mucosal Immunity, GBF-German Research Center for Biotechnology, Mascheroder Weg 1, 38124 Braunschweig, Germany.
Nucleic Acids Res. 2004 Dec 16;32(22):6643-9. doi: 10.1093/nar/gkh1009. Print 2004.
Recent studies of genome-wide transcriptional regulatory network (TRN) revealed several intriguing structural and dynamic features of gene expression at a system level. Unfortunately, the network under study is often far from complete. A critical question is thus how much the network is incomplete and to what extent this would affect the results of analysis. Here we compare the Escherichia coli TRN built by Shen-Orr et al. (Nature Genet., 31, 64-68) with two TRNs reconstructed from RegulonDB and Ecocyc respectively and present an extended E.coli TRN by integrating information from these databases and literature. The scale of the extended TRN is about twice as large as the previous ones. The new network preserves the multi-layer hierarchical structure which we recently reported but has more layers. More global regulators are inferred. While the feed forward loop (FFL) is confirmed to be highly representative in the network, the distribution of the different types of FFLs is different from that based on the incomplete network. In contrast to the notion of motif aggregation and formation of homologous motif clusters, we found that most FFLs interact and form a giant motif cluster. Furthermore, we show that only a small portion of the genes is solely regulated by only one FFL. Many genes are regulated by two or more interacting FFLs or other more complicated network motifs together with transcriptional factors not belonging to any network motifs, thereby forming complex regulatory circuits. Overall, the extended TRN represents a more solid basis for structural and functional analysis of genome-wide gene regulation in E.coli.
最近对全基因组转录调控网络(TRN)的研究揭示了系统水平上基因表达的几个有趣的结构和动态特征。不幸的是,所研究的网络往往远非完整。因此,一个关键问题是该网络的不完整性程度如何,以及这将在多大程度上影响分析结果。在这里,我们将Shen-Orr等人构建的大肠杆菌TRN(《自然遗传学》,第31卷,第64 - 68页)与分别从RegulonDB和Ecocyc重建的两个TRN进行比较,并通过整合来自这些数据库和文献的信息,呈现一个扩展的大肠杆菌TRN。扩展后的TRN规模约为之前的两倍。新网络保留了我们最近报道的多层层次结构,但层数更多。推断出了更多的全局调控因子。虽然前馈环(FFL)在网络中被证实具有高度代表性,但不同类型FFL的分布与基于不完整网络的分布不同。与基序聚集和同源基序簇形成的概念相反,我们发现大多数FFL相互作用并形成一个巨大的基序簇。此外,我们表明只有一小部分基因仅由一个FFL单独调控。许多基因由两个或更多相互作用的FFL或其他更复杂的网络基序以及不属于任何网络基序的转录因子共同调控,从而形成复杂的调控回路。总体而言,扩展后的TRN为大肠杆菌全基因组基因调控的结构和功能分析提供了更坚实的基础。