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Integrative inference of gene-regulatory networks in Escherichia coli using information theoretic concepts and sequence analysis

机译:利用信息理论和序列分析方法对大肠埃希菌基因调控网络进行综合推断

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Background Although Escherichia coli is one of the best studied model organisms, a comprehensive understanding of its gene regulation is not yet achieved. There exist many approaches to reconstruct regulatory interaction networks from gene expression experiments. Mutual information based approaches are most useful for large-scale network inference. Results We used a three-step approach in which we combined gene regulatory network inference based on directed information (DTI) and sequence analysis. DTI values were calculated on a set of gene expression profiles from 19 time course experiments extracted from the Many Microbes Microarray Database. Focusing on influences between pairs of genes in which one partner encodes a transcription factor (TF) we derived a network which contains 878 TF - gene interactions of which 166 are known according to RegulonDB. Afterward, we selected a subset of 109 interactions that could be confirmed by the presence of a phylogenetically conserved binding site of the respective regulator. By this second step, the fraction of known interactions increased from 19% to 60%. In the last step, we checked the 44 of the 109 interactions not yet included in RegulonDB for functional relationships between the regulator and the target and, thus, obtained ten TF - target gene interactions. Five of them concern the regulator LexA and have already been reported in the literature. The remaining five influences describe regulations by Fis (with two novel targets), PhdR, PhoP, and KdgR. For the validation of our approach, one of them, the regulation of lipoate synthase (LipA) by the pyruvate-sensing pyruvate dehydrogenate repressor (PdhR), was experimentally checked and confirmed. Conclusions We predicted a set of five novel TF - target gene interactions in E. coli. One of them, the regulation of lipA by the transcriptional regulator PdhR was validated experimentally. Furthermore, we developed DTInfer, a new R-package for the inference of gene-regulatory networks from microarrays using directed information.
机译:背景技术尽管大肠杆菌是研究最深入的模型生物之一,但尚未对其基因调控获得全面的了解。存在许多从基因表达实验重建调控相互作用网络的方法。基于互信息的方法对于大规模网络推断最为有用。结果我们采用了三步法,其中我们将基于定向信息(DTI)和序列分析的基因调控网络推论相结合。 DTI值是根据从许多微生物微阵列数据库中提取的19个时程实验中的一组基因表达谱计算得出的。着眼于一对伴侣编码转录因子(TF)的基因对之间的影响,我们得出了一个包含878 TF的网络-根据RegulonDB已知其中166个基因相互作用。之后,我们选择了109种相互作用的子集,可以通过相应调节子的系统发育保守结合位点的存在来确认。通过第二步,已知相互作用的比例从19%增加到60%。在最后一步中,我们检查了RegulonDB中尚未包括的109种相互作用中的44种,以了解调节剂与靶标之间的功能关系,从而获得10种TF-靶基因相互作用。其中有五个涉及监管机构LexA,并且已有文献报道。其余五种影响描述了Fis(具有两个新颖的目标)的法规PhdR,PhoP和KdgR。为了验证我们的方法,其中之一是通过丙酮酸敏感的丙酮酸脱氢阻遏物(PdhR)对脂酸合酶(LipA)的调节进行了实验检查和确认。结论我们预测了在大肠杆菌中的五个新的TF-靶基因相互作用的集合。其中之一是转录调节因子PdhR对lipA的调节作用已通过实验验证。此外,我们开发了DTInfer,这是一个新的R包,用于使用定向信息从微阵列推断基因调控网络。

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