Department of Chemistry , the Pennsylvania State University , University Park , Pennsylvania 16802 , United States.
ACS Chem Biol. 2019 Mar 15;14(3):506-515. doi: 10.1021/acschembio.9b00018. Epub 2019 Feb 22.
The nucleosome, the fundamental gene-packing unit comprising an octameric histone protein core wrapped with DNA, has a flexible structure that enables dynamic gene regulation mechanisms. Histone lysine acetylation at H3K56 removes a positive charge from the histone core where it interacts with the termini of the nucleosomal DNA and acts as a critical gene regulatory signal that is implicated in transcription initiation and elongation. The predominant proposal for the biophysical role of H3K56 acetylation (H3K56ac) is that weakened electrostatic interaction between DNA termini and the histone core results in facilitated opening and subsequent disassembly of the nucleosome. However, this effect alone is too weak to account for the strong coupling between H3K56ac and its regulatory outcomes. Here we utilized a semisynthetically modified nucleosome with H3K56ac in order to address this discrepancy. Based on the results, we propose an innovative mechanism by which the charge neutralization effect of H3K56ac is significantly amplified via protein binding. We employed three-color single-molecule fluorescence resonance energy transfer (smFRET) to monitor the opening rate of nucleosomal DNA termini induced by binding of histone chaperone Nap1. We observed an elevated opening rate upon H3K56ac by 5.9-fold, which is far larger than the 1.5-fold previously reported for the spontaneous opening dynamics in the absence of Nap1. Our proposed mechanism successfully reconciles this discrepancy because DNA opening for Nap1 binding must be larger than the average spontaneous opening. This is a novel mechanism that can explain how a small biophysical effect of histone acetylation results in a significant change in protein binding rate.
核小体是一种基本的基因包装单元,由包裹着 DNA 的八聚体组蛋白核心组成,具有灵活的结构,能够实现动态的基因调控机制。组蛋白赖氨酸在 H3K56 上的乙酰化会从与核小体 DNA 末端相互作用的组蛋白核心中去除正电荷,作为一个关键的基因调控信号,它参与转录起始和延伸。H3K56 乙酰化(H3K56ac)的主要生物物理作用假设是 DNA 末端与组蛋白核心之间的静电相互作用减弱,导致核小体更容易打开,随后解体。然而,这种单一的作用太弱,无法解释 H3K56ac 与其调控结果之间的强耦合。在这里,我们利用半合成修饰的核小体来研究 H3K56ac,以解决这一差异。基于这些结果,我们提出了一个创新的机制,通过蛋白质结合显著放大了 H3K56ac 的电荷中和效应。我们采用三色单分子荧光共振能量转移(smFRET)来监测组蛋白伴侣 Nap1 结合诱导的核小体 DNA 末端的打开速率。我们观察到 H3K56ac 的打开速率提高了 5.9 倍,这远远大于之前报道的在没有 Nap1 的情况下自发打开动力学的 1.5 倍。我们提出的机制成功地解释了这种差异,因为 Nap1 结合的 DNA 打开必须大于平均自发打开。这是一种新的机制,可以解释组蛋白乙酰化的小生物物理效应如何导致蛋白质结合速率的显著变化。