Yamada Naomi, Kuntala Prashant Kumar, Pugh B Franklin, Mahony Shaun
Center for Eukaryotic Gene Regulation, Department of Biochemistry & Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania.
J Comput Biol. 2020 Mar;27(3):429-435. doi: 10.1089/cmb.2019.0466. Epub 2020 Feb 5.
Regulatory proteins can employ multiple direct and indirect modes of interaction with the genome. The ChIP-exo mixture model (ChExMix) provides a principled approach to detecting multiple protein-DNA interaction modes in a single ChIP-exo experiment. ChExMix discovers and characterizes binding event subtypes in ChIP-exo data by leveraging both protein-DNA cross-linking signatures and DNA motifs. In this study, we present a summary of the major features and applications of ChExMix. We demonstrate that ChExMix does not require high-resolution protein-DNA binding assay data to detect binding event subtypes. Specifically, we apply ChExMix to analyze 393 ChIP-seq data profiles in K562 cells. Similar binding event subtypes are discovered across multiple proteins, suggesting the existence of colocalized regulatory protein modules that are recruited to DNA through a particular sequence-specific transcription factor. Our results thus suggest that ChExMix can characterize protein-DNA binding interaction modes using data from multiple types of protein-DNA interaction assays.
调控蛋白可采用多种与基因组直接和间接的相互作用方式。染色质免疫沉淀结合外显子测序混合模型(ChExMix)提供了一种在单个染色质免疫沉淀结合外显子测序实验中检测多种蛋白质 - DNA相互作用模式的原则性方法。ChExMix通过利用蛋白质 - DNA交联特征和DNA基序来发现并表征染色质免疫沉淀结合外显子测序数据中的结合事件亚型。在本研究中,我们总结了ChExMix的主要特征和应用。我们证明ChExMix不需要高分辨率的蛋白质 - DNA结合检测数据来检测结合事件亚型。具体而言,我们应用ChExMix分析K562细胞中的393个染色质免疫沉淀测序(ChIP-seq)数据概况。在多种蛋白质中发现了相似的结合事件亚型,这表明存在通过特定序列特异性转录因子被招募到DNA上的共定位调控蛋白模块。因此,我们的结果表明ChExMix可以使用来自多种类型蛋白质 - DNA相互作用检测的数据来表征蛋白质 - DNA结合相互作用模式。