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Integrated analysis of regulatory and metabolic networks reveals novel regulatory mechanisms in Saccharomyces cerevisiae

机译:调节和代谢网络的综合分析揭示了酿酒酵母中新的调节机制

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摘要

We describe the use of model-driven analysis of multiple data types relevant to transcriptional regulation of metabolism to discover novel regulatory mechanisms in Saccharomyces cerevisiae. We have reconstructed the nutrient-controlled transcriptional regulatory network controlling metabolism in S. cerevisiae consisting of 55 transcription factors regulating 750 metabolic genes, based on information in the primary literature. This reconstructed regulatory network coupled with an existing genome-scale metabolic network model allows in silico prediction of growth phenotypes of regulatory gene deletions as well as gene expression profiles. We compared model predictions of gene expression changes in response to genetic and environmental perturbations to experimental data to identify potential novel targets for transcription factors. We then identified regulatory cascades connecting transcription factors to the potential targets through a systematic model expansion strategy using published genome-wide chromatin immunoprecipitation and binding-site-motif data sets. Finally, we show the ability of an integrated metabolic and regulatory network model to predict growth phenotypes of transcription factor knockout strains. These studies illustrate the potential of model-driven data integration to systematically discover novel components and interactions in regulatory and metabolic networks in eukaryotic cells.
机译:我们描述了与代谢的转录调控有关的多种数据类型的模型驱动分析的使用,以发现酿酒酵母中的新型调控机制。我们已根据原始文献中的信息,重建了由啤酒酵母组成的营养控制转录调控网络,该网络由55个转录因子调控750个代谢基因组成。这种重构的调控网络与现有的基因组规模的代谢网络模型相结合,可以对调控基因缺失的生长表型以及基因表达谱进行计算机预测。我们将基因表达响应遗传和环境扰动的模型预测与实验数据进行了比较,以确定潜在的新型靶标转录因子。然后,我们使用已发布的全基因组染色质免疫沉淀和结合位点基序数据集,通过系统的模型扩展策略,确定了将转录因子连接到潜在靶标的调控级联反应。最后,我们展示了整合的代谢和调控网络模型预测转录因子敲除菌株的生长表型的能力。这些研究说明了模型驱动的数据集成潜在地系统地发现真核细胞中调节和代谢网络中的新成分和相互作用的潜力。

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