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Nucleosome conformational variability in solution and in interphase nuclei evidenced by cryo-electron microscopy of vitreous sections

机译:玻璃体切片的冷冻电子显微镜观察证明溶液和相间核中的核小体构象变异

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摘要

In Eukaryotes, DNA is wound around the histone octamer forming the basic chromatin unit, the nucleosome. Atomic structures have been obtained from crystallography and single particle cryo-electron microscopy (cryoEM) of identical engineered particles. But native nucleosomes are dynamical entities with diverse DNA sequence and histone content, and little is known about their conformational variability, especially in the cellular context. Using cryoEM and tomography of vitreous sections we analyse native nucleosomes, both in vitro, using purified particles solubilized at physiologically relevant concentrations (25–50%), and in situ, within interphase nuclei. We visualize individual nucleosomes at a level of detail that allows us to measure the distance between the DNA gyres wrapped around. In concentrated solutions, we demonstrate a salt-dependent transition, with a high salt compact conformation resembling the canonical nucleosome and an open low salt one, closer to nuclear nucleosomes. Although further particle characterization and cartography are needed to understand the relationship between this conformational variability and chromatin functional states, this work opens a route to chromatin exploration in situ.
机译:在真核生物中,DNA缠绕在组蛋白八聚体周围,形成基本的染色质单位,即核小体。原子结构已经从晶体学和相同工程颗粒的单颗粒低温电子显微镜(cryoEM)中获得。但是天然核小体是具有不同DNA序列和组蛋白含量的动力学实体,对其构象变异性知之甚少,尤其是在细胞环境中。使用cryoEM和玻璃体断层扫描,我们可以分析体外的天然核小体,既可以使用在生理上相关浓度(25%至50%)溶解的纯化颗粒,也可以在相间核内原位分析。我们以详细程度可视化单个核小体,使我们能够测量缠绕的DNA回旋体之间的距离。在浓缩溶液中,我们证明了盐依赖性过渡,具有类似于规范核小体的高盐紧密构象和接近核核小体的开放低盐盐构象。尽管需要进一步的颗粒表征和制图来了解这种构象变异性与染色质功能状态之间的关系,但这项工作为染色质原位探索开辟了道路。

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