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核小体相关蛋白 fis 与 DNA 的结合受 DNA 呼吸动力学的调节。

Binding of nucleoid-associated protein fis to DNA is regulated by DNA breathing dynamics.

机构信息

Bioscience Division, Los Alamos National Laboratory, Los Alamos, New Mexico, USA.

出版信息

PLoS Comput Biol. 2013;9(1):e1002881. doi: 10.1371/journal.pcbi.1002881. Epub 2013 Jan 17.

Abstract

Physicochemical properties of DNA, such as shape, affect protein-DNA recognition. However, the properties of DNA that are most relevant for predicting the binding sites of particular transcription factors (TFs) or classes of TFs have yet to be fully understood. Here, using a model that accurately captures the melting behavior and breathing dynamics (spontaneous local openings of the double helix) of double-stranded DNA, we simulated the dynamics of known binding sites of the TF and nucleoid-associated protein Fis in Escherichia coli. Our study involves simulations of breathing dynamics, analysis of large published in vitro and genomic datasets, and targeted experimental tests of our predictions. Our simulation results and available in vitro binding data indicate a strong correlation between DNA breathing dynamics and Fis binding. Indeed, we can define an average DNA breathing profile that is characteristic of Fis binding sites. This profile is significantly enriched among the identified in vivo E. coli Fis binding sites. To test our understanding of how Fis binding is influenced by DNA breathing dynamics, we designed base-pair substitutions, mismatch, and methylation modifications of DNA regions that are known to interact (or not interact) with Fis. The goal in each case was to make the local DNA breathing dynamics either closer to or farther from the breathing profile characteristic of a strong Fis binding site. For the modified DNA segments, we found that Fis-DNA binding, as assessed by gel-shift assay, changed in accordance with our expectations. We conclude that Fis binding is associated with DNA breathing dynamics, which in turn may be regulated by various nucleotide modifications.

摘要

DNA 的理化性质,如形状,会影响蛋白-DNA 的识别。然而,对于预测特定转录因子 (TF) 或 TF 类的结合位点最相关的 DNA 性质,尚未被完全理解。在这里,我们使用一种能够准确捕捉双链 DNA 熔融行为和呼吸动力学(双链螺旋自发局部打开)的模型,模拟了 TF 和核小体相关蛋白 Fis 在大肠杆菌中的已知结合位点的动力学。我们的研究涉及呼吸动力学模拟、对大量已发表的体外和基因组数据集的分析,以及对我们预测的靶向实验测试。我们的模拟结果和可用的体外结合数据表明,DNA 呼吸动力学与 Fis 结合之间存在很强的相关性。实际上,我们可以定义一个平均的 DNA 呼吸特征图谱,这是 Fis 结合位点的特征。该图谱在鉴定的大肠杆菌 Fis 结合位点中显著富集。为了检验我们对 Fis 结合如何受 DNA 呼吸动力学影响的理解,我们设计了碱基对取代、错配和甲基化修饰的 DNA 区域,这些区域已知与 Fis 相互作用(或不相互作用)。在每种情况下,目标都是使局部 DNA 呼吸动力学更接近或远离与强 Fis 结合位点相关的呼吸特征图谱。对于修饰后的 DNA 片段,我们发现凝胶迁移分析评估的 Fis-DNA 结合根据我们的预期发生了变化。我们得出结论,Fis 结合与 DNA 呼吸动力学相关,而后者又可能受到各种核苷酸修饰的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47be/3547798/e9575598bf22/pcbi.1002881.g001.jpg

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