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Predicting eukaryotic transcriptional cooperativity by Bayesian network integration of genome-wide data.

机译:通过全基因组数据的贝叶斯网络整合预测真核转录的协同性。

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Transcriptional cooperativity among several transcription factors (TFs) is believed to be the main mechanism of complexity and precision in transcriptional regulatory programs. Here, we present a Bayesian network framework to reconstruct a high-confidence whole-genome map of transcriptional cooperativity in Saccharomyces cerevisiae by integrating a comprehensive list of 15 genomic features. We design a Bayesian network structure to capture the dominant correlations among features and TF cooperativity, and introduce a supervised learning framework with a well-constructed gold-standard dataset. This framework allows us to assess the predictive power of each genomic feature, validate the superior performance of our Bayesian network compared to alternative methods, and integrate genomic features for optimal TF cooperativity prediction. Data integration reveals 159 high-confidence predicted cooperative relationships among 105 TFs, most of which are subsequently validated by literature search. The existing and predicted transcriptional cooperativities can be grouped into three categories based on the combination patterns of the genomic features, providing further biological insights into the different types of TF cooperativity. Our methodology is the first supervised learning approach for predicting transcriptional cooperativity, compares favorably to alternative unsupervised methodologies, and can be applied to other genomic data integration tasks where high-quality gold-standard positive data are scarce.
机译:几个转录因子(TF)之间的转录合作性被认为是转录调控程序中复杂性和精确性的主要机制。在这里,我们提出了一个贝叶斯网络框架,通过整合15个基因组特征的完整列表来重建酿酒酵母转录合作性的高可信度全基因组图谱。我们设计了一种贝叶斯网络结构,以捕获特征和TF合作性之间的主导关系,并引入具有良好构建的金标准数据集的监督学习框架。该框架使我们能够评估每个基因组特征的预测能力,验证贝叶斯网络与其他方法相比的优越性能,并整合基因组特征以实现最佳TF合作性预测。数据整合揭示了105个TF之间的159个高可信度预测的合作关系,其中大多数随后都通过文献检索得到了验证。基于基因组特征的组合模式,可以将现有和预测的转录合作性分为三类,从而为TF合作性的不同类型提供进一步的生物学见解。我们的方法是用于预测转录合作性的第一种监督学习方法,与替代的无监督方法相比具有优势,并且可以应用于缺乏高质量金标准阳性数据的其他基因组数据整合任务。

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