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亚核小体基因组结构揭示了独特的核小体折叠模式。

Sub-nucleosomal Genome Structure Reveals Distinct Nucleosome Folding Motifs.

机构信息

Laboratory for Cell Systems Control, RIKEN Center for Biosystems Dynamics Research, 6-2-3 Furuedai, Suita, Osaka 565-0874, Japan.

Laboratory for Biomolecular Function Simulation, Quantitative Biology Center, RIKEN, 6-7-1 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.

出版信息

Cell. 2019 Jan 24;176(3):520-534.e25. doi: 10.1016/j.cell.2018.12.014. Epub 2019 Jan 17.

Abstract

Elucidating the global and local rules that govern genome-wide, hierarchical chromatin architecture remains a critical challenge. Current high-throughput chromosome conformation capture (Hi-C) technologies have identified large-scale chromatin structural motifs, such as topologically associating domains and looping. However, structural rules at the smallest or nucleosome scale remain poorly understood. Here, we coupled nucleosome-resolved Hi-C technology with simulated annealing-molecular dynamics (SA-MD) simulation to reveal 3D spatial distributions of nucleosomes and their genome-wide orientation in chromatin. Our method, called Hi-CO, revealed distinct nucleosome folding motifs across the yeast genome. Our results uncovered two types of basic secondary structural motifs in nucleosome folding: α-tetrahedron and β-rhombus analogous to α helix and β sheet motifs in protein folding. Using mutants and cell-cycle-synchronized cells, we further uncovered motifs with specific nucleosome positioning and orientation coupled to epigenetic features at individual loci. By illuminating molecular-level structure-function relationships in eukaryotic chromatin, our findings establish organizational principles of nucleosome folding.

摘要

阐明控制全基因组层次化染色质结构的全局和局部规则仍然是一个关键挑战。目前的高通量染色体构象捕获(Hi-C)技术已经确定了大规模染色质结构基序,如拓扑关联域和环。然而,在最小的核小体尺度或核小体尺度上的结构规则仍然知之甚少。在这里,我们将核小体分辨 Hi-C 技术与模拟退火-分子动力学(SA-MD)模拟相结合,以揭示核小体在染色质中的三维空间分布及其在基因组上的取向。我们的方法称为 Hi-CO,揭示了酵母基因组中不同的核小体折叠基序。我们的结果揭示了核小体折叠中的两种基本二级结构基序:类似于蛋白质折叠中α螺旋和β片层的α四面体和β菱形。使用突变体和细胞周期同步化的细胞,我们进一步揭示了与特定核小体定位和取向相关的基序,并与单个基因座的表观遗传特征相关联。通过阐明真核染色质中分子水平的结构-功能关系,我们的发现建立了核小体折叠的组织原则。

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