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捕捉染色质纤维中的结构异质性。

Capturing Structural Heterogeneity in Chromatin Fibers.

作者信息

Ekundayo Babatunde, Richmond Timothy J, Schalch Thomas

机构信息

Department of Molecular Biology, Faculty of Sciences, University of Geneva, CH-1211 Geneva 4, Switzerland; Institute of Genetics and Genomics of Geneva (iGE3), University of Geneva, CH-1211 Geneva 4, Switzerland.

Institute of Molecular Biology and Biophysics, Department of Biology, Swiss Federal Institute of Technology Zurich, CH-8093 Zurich, Switzerland.

出版信息

J Mol Biol. 2017 Oct 13;429(20):3031-3042. doi: 10.1016/j.jmb.2017.09.002. Epub 2017 Sep 9.

Abstract

Chromatin fiber organization is implicated in processes such as transcription, DNA repair and chromosome segregation, but how nucleosomes interact to form higher-order structure remains poorly understood. We solved two crystal structures of tetranucleosomes with approximately 11-bp DNA linker length at 5.8 and 6.7 Å resolution. Minimal intramolecular nucleosome-nucleosome interactions result in a fiber model resembling a flat ribbon that is compatible with a two-start helical architecture, and that exposes histone and DNA surfaces to the environment. The differences in the two structures combined with electron microscopy reveal heterogeneous structural states, and we used site-specific chemical crosslinking to assess the diversity of nucleosome-nucleosome interactions through identification of structure-sensitive crosslink sites that provide a means to characterize fibers in solution. The chromatin fiber architectures observed here provide a basis for understanding heterogeneous chromatin higher-order structures as they occur in a genomic context.

摘要

染色质纤维组织与转录、DNA修复和染色体分离等过程有关,但核小体如何相互作用形成高阶结构仍知之甚少。我们解析了两个连接DNA长度约为11bp的四核小体的晶体结构,分辨率分别为5.8 Å和6.7 Å。分子内核小体-核小体间的最小相互作用产生了一种类似于扁平带的纤维模型,该模型与双起始螺旋结构兼容,并将组蛋白和DNA表面暴露于环境中。两种结构的差异与电子显微镜结果相结合揭示了结构的异质性状态,我们使用位点特异性化学交联通过鉴定对结构敏感的交联位点来评估核小体-核小体相互作用的多样性,这些位点为表征溶液中的纤维提供了一种方法。此处观察到的染色质纤维结构为理解基因组背景下的异质染色质高阶结构提供了基础。

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