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A Context-Specific Network of Protein-DNA and Protein-Protein Interactions Reveals New Regulatory Motifs in Human B Cells

机译:特异性蛋白质-DNA和蛋白质 - 蛋白质相互作用网络揭示了人B细胞中的新调节基序

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Recent genome wide studies in yeast have started to unravel the complex, combinatorial nature of transcriptional regulation in eukaryotic cells, including the concerted regulation of proteins involved in complex formation. In this work, we use a Bayesian evidence integration framework to assemble an integrated network, including both protein-DNA and protein-protein interactions, in a specific cellular context(human B cells). We then use it to study common interaction motifs between protein complexes and regulatory programs, using an enrichment analysis approach. Specifically, we compare the frequency of mixed interaction motifs in the real network against random networks of equivalent connectivity. These motifs include sets of target genes regulated by multiple interacting transcription factors, and gene sets encoding same complex proteins regulated by different transcription factors.
机译:近期基因组在酵母中的研究已经开始解开了真核细胞中转录调节的复杂,包括蛋白质的齐节调节。在这项工作中,我们使用贝叶斯证据整合框架来组装综合网络,包括蛋白质-DNA和蛋白质 - 蛋白质相互作用,在特定的细胞上下文(人B细胞)中。然后,我们使用浓缩分析方法研究蛋白质复合体和监管计划之间的常见相互作用基序。具体地,我们将真实网络中的混合交互基节的频率与等效连通性的随机网络进行比较。这些基序包括由多个相互作用转录因子调节的靶基因组,并且编码由不同转录因子调节的相同复合蛋白的基因组。

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