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Detection of cooperatively bound transcription factor pairs using ChIP-seq peak intensities and expectation maximization

机译:使用芯片-SEQ峰值强度检测协同结合转录因子对的峰值强度和期望最大化

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摘要

Transcription factors (TFs) often work cooperatively, where the binding of one TF to DNA enhances the binding affinity of a second TF to a nearby location. Such cooperative binding is important for activating gene expression from promoters and enhancers in both prokaryotic and eukaryotic cells. Existing methods to detect cooperative binding of a TF pair rely on analyzing the sequence that is bound. We propose a method that uses, instead, only ChIP-seq peak intensities and an expectation maximization (CPI-EM) algorithm. We validate our method using ChIP-seq data from cells where one of a pair of TFs under consideration has been genetically knocked out. Our algorithm relies on our observation that cooperative TF-TF binding is correlated with weak binding of one of the TFs, which we demonstrate in a variety of cell types, including E. coli, S. cerevisiae and M. musculus cells. We show that this method performs significantly better than a predictor based only on the ChIP-seq peak distance of the TFs under consideration. This suggests that peak intensities contain information that can help detect the cooperative binding of a TF pair. CPI-EM also outperforms an existing sequence-based algorithm in detecting cooperative binding. The CPI-EM algorithm is available at https://github.com/vishakad/cpi-em.
机译:转录因子(TFS)通常协同工作,其中一个TF与DNA的结合增强了第二个TF到附近位置的结合亲和力。这种合作结合对于激活来自原发性和真核细胞中的启动子和增强子的激活基因表达是重要的。检测TF对协同绑定的现有方法依赖于分析绑定的序列。我们提出了一种使用的方法,而是仅使用芯片SEQ峰值强度和期望最大化(CPI-EM)算法。我们使用来自芯片的芯片-SEQ数据验证我们的方法,其中一对正在考虑的TFS中的一个已被遗传淘汰。我们的算法依赖于我们的观察,即合作的TF-TF结合与其中一种TFS的弱结合相关,我们在各种细胞类型中展示,包括大肠杆菌,S.酿酒酵母和M. Musculus细胞。我们表明该方法仅仅基于所考虑的TFS的芯片-SEQ峰值距离而显着优于预测器。这表明峰强度包含可以有助于检测TF对的协同绑定的信息。 CPI-EM还优于检测合作绑定的现有序列的算法。 CPI-EM算法在https://github.com/vishakad/cpi-em中提供。

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