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核小体、连接DNA和连接组蛋白形成一种独特的结构基序,指导染色质的高级折叠和压缩。

Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin.

作者信息

Bednar J, Horowitz R A, Grigoryev S A, Carruthers L M, Hansen J C, Koster A J, Woodcock C L

机构信息

Department of Biology, University of Massachusetts, Amherst, MA 01003, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14173-8. doi: 10.1073/pnas.95.24.14173.

Abstract

The compaction level of arrays of nucleosomes may be understood in terms of the balance between the self-repulsion of DNA (principally linker DNA) and countering factors including the ionic strength and composition of the medium, the highly basic N termini of the core histones, and linker histones. However, the structural principles that come into play during the transition from a loose chain of nucleosomes to a compact 30-nm chromatin fiber have been difficult to establish, and the arrangement of nucleosomes and linker DNA in condensed chromatin fibers has never been fully resolved. Based on images of the solution conformation of native chromatin and fully defined chromatin arrays obtained by electron cryomicroscopy, we report a linker histone-dependent architectural motif beyond the level of the nucleosome core particle that takes the form of a stem-like organization of the entering and exiting linker DNA segments. DNA completes approximately 1.7 turns on the histone octamer in the presence and absence of linker histone. When linker histone is present, the two linker DNA segments become juxtaposed approximately 8 nm from the nucleosome center and remain apposed for 3-5 nm before diverging. We propose that this stem motif directs the arrangement of nucleosomes and linker DNA within the chromatin fiber, establishing a unique three-dimensional zigzag folding pattern that is conserved during compaction. Such an arrangement with peripherally arranged nucleosomes and internal linker DNA segments is fully consistent with observations in intact nuclei and also allows dramatic changes in compaction level to occur without a concomitant change in topology.

摘要

核小体阵列的压缩程度可以通过DNA(主要是连接DNA)的自排斥与包括介质的离子强度和组成、核心组蛋白的高碱性N端以及连接组蛋白在内的对抗因素之间的平衡来理解。然而,从松散的核小体链转变为紧密的30纳米染色质纤维过程中起作用的结构原理一直难以确定,并且浓缩染色质纤维中核小体和连接DNA的排列从未得到完全解析。基于通过电子冷冻显微镜获得的天然染色质和完全确定的染色质阵列的溶液构象图像,我们报道了一种依赖连接组蛋白的结构基序,其超出了核小体核心颗粒的水平,呈进入和退出的连接DNA片段的茎状组织形式。在有和没有连接组蛋白的情况下,DNA在组蛋白八聚体上完成约1.7圈缠绕。当存在连接组蛋白时,两个连接DNA片段在距离核小体中心约8纳米处并列,并在分开前保持3 - 5纳米的并列状态。我们提出,这种茎状基序指导染色质纤维内核小体和连接DNA的排列,建立一种在压缩过程中保守的独特三维锯齿状折叠模式。这种外周排列核小体和内部连接DNA片段的排列与在完整细胞核中的观察结果完全一致,并且还允许在不伴随拓扑结构变化的情况下发生压缩程度的显著变化。

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本文引用的文献

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Chromatin organization re-viewed.染色质组织再审视。
Trends Cell Biol. 1995 Jul;5(7):272-7. doi: 10.1016/s0962-8924(00)89038-8.
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