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Widespread evidence of cooperative DNA binding by transcription factors in Drosophila development

机译:果蝇发育过程中转录因子协同DNA结合的广泛证据

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Regulation of eukaryotic gene transcription is often combinatorial in nature, with multiple transcription factors (TFs) regulating common target genes, often through direct or indirect mutual interactions. Many individual examples of cooperative binding by directly interacting TFs have been identified, but it remains unclear how pervasive this mechanism is during animal development. Cooperative TF binding should be manifest in genomic sequences as biased arrangements of TF-binding sites. Here, we explore the extent and diversity of such arrangements related to gene regulation during Drosophila embryogenesis. We used the DNA-binding specificities of 322 TFs along with chromatin accessibility information to identify enriched spacing and orientation patterns of TF-binding site pairs. We developed a new statistical approach for this task, specifically designed to accurately assess inter-site spacing biases while accounting for the phenomenon of homotypic site clustering commonly observed in developmental regulatory regions. We observed a large number of short-range distance preferences between TF-binding site pairs, including examples where the preference depends on the relative orientation of the binding sites. To test whether these binding site patterns reflect physical interactions between the corresponding TFs, we analyzed 27 TF pairs whose binding sites exhibited short distance preferences. In vitro protein-protein binding experiments revealed that > 65% of these TF pairs can directly interact with each other. For five pairs, we further demonstrate that they bind cooperatively to DNA if both sites are present with the preferred spacing. This study demonstrates how DNA-binding motifs can be used to produce a comprehensive map of sequence signatures for different mechanisms of combinatorial TF action.
机译:真核基因转录的调控本质上通常是组合的,通常通过直接或间接的相互作用,多种转录因子(TF)调控共同的靶基因。已经确定了通过直接相互作用的TFs进行合作结合的许多单独实例,但尚不清楚该机制在动物发育过程中的普遍性。合作TF结合应在基因组序列中表现为TF结合位点的有序排列。在这里,我们探索果蝇胚胎发生过程中与基因调控相关的这种安排的程度和多样性。我们使用322 TFs的DNA结合特异性以及染色质可及性信息来鉴定TF结合位点对的富集的间隔和方向模式。我们为此任务开发了一种新的统计方法,该方法专门设计用于准确评估站点间间距偏差,同时解决在发育调控区域中常见的同型站点聚类现象。我们观察到TF结合位点对之间的大量短距离距离偏好,包括其中偏好取决于结合位点的相对方向的示例。为了测试这些结合位点模式是否反映了相应TF之间的物理相互作用,我们分析了27个TF对,其结合位点表现出短距离偏好。体外蛋白质-蛋白质结合实验表明,这些TF对中> 65%可以直接相互相互作用。对于五对,我们进一步证明,如果两个位点均以优选的间隔存在,则它们将与DNA协同结合。这项研究表明如何结合DNA结合基序可用于产生组合TF作用的不同机制的序列签名的全面图。

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