In Silico Biomolecular Structure and Dynamics Group, Hubrecht Institute, Utrecht, The Netherlands.
Department of Cellular and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
PLoS Comput Biol. 2021 Jun 3;17(6):e1009013. doi: 10.1371/journal.pcbi.1009013. eCollection 2021 Jun.
Genomic DNA is packaged in chromatin, a dynamic fiber variable in size and compaction. In chromatin, repeating nucleosome units wrap 145-147 DNA basepairs around histone proteins. Genetic and epigenetic regulation of genes relies on structural transitions in chromatin which are driven by intra- and inter-nucleosome dynamics and modulated by chemical modifications of the unstructured terminal tails of histones. Here we demonstrate how the interplay between histone H3 and H2A tails control ample nucleosome breathing motions. We monitored large openings of two genomic nucleosomes, and only moderate breathing of an engineered nucleosome in atomistic molecular simulations amounting to 24 μs. Transitions between open and closed nucleosome conformations were mediated by the displacement and changes in compaction of the two histone tails. These motions involved changes in the DNA interaction profiles of clusters of epigenetic regulatory aminoacids in the tails. Removing the histone tails resulted in a large increase of the amplitude of nucleosome breathing but did not change the sequence dependent pattern of the motions. Histone tail modulated nucleosome breathing is a key mechanism of chromatin dynamics with important implications for epigenetic regulation.
基因组 DNA 被包装在染色质中,这是一种大小和紧密度可变的动态纤维。在染色质中,重复的核小体单元将 145-147 个 DNA 碱基对围绕组蛋白蛋白包裹起来。基因的遗传和表观遗传调控依赖于染色质的结构转变,这些转变由核小体内部和核小体之间的动力学驱动,并受组蛋白无规卷曲末端化学修饰的调节。在这里,我们展示了组蛋白 H3 和 H2A 尾部之间的相互作用如何控制丰富的核小体呼吸运动。我们在原子分子模拟中监测了两个基因组核小体的大开口,以及一个工程核小体的适度呼吸,总共达到 24 μs。核小体构象的开和闭之间的转变是由两个组蛋白尾部的位移和压缩变化介导的。这些运动涉及到尾部中簇集的表观遗传调节氨基酸的 DNA 相互作用模式的变化。去除组蛋白尾部会导致核小体呼吸幅度的大幅增加,但不会改变运动的序列依赖性模式。组蛋白尾部调节的核小体呼吸是染色质动力学的关键机制,对表观遗传调控具有重要意义。