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核小体 DNA 的惊人扭曲及其对高级折叠的影响。

Surprising Twists in Nucleosomal DNA with Implication for Higher-order Folding.

机构信息

Department of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.

Department of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.

出版信息

J Mol Biol. 2021 Sep 3;433(18):167121. doi: 10.1016/j.jmb.2021.167121. Epub 2021 Jun 28.

Abstract

While nucleosomes are dynamic entities that must undergo structural deformations to perform their functions, the general view from available high-resolution structures is a largely static one. Even though numerous examples of twist defects have been documented, the DNA wrapped around the histone core is generally thought to be overtwisted. Analysis of available high-resolution structures from the Protein Data Bank reveals a heterogeneous distribution of twist along the nucleosomal DNA, with clear patterns that are consistent with the literature, and a significant fraction of structures that are undertwisted. The subtle differences in nucleosomal DNA folding, which extend beyond twist, have implications for nucleosome disassembly and modeled higher-order structures. Simulations of oligonucleosome arrays built with undertwisted models behave very differently from those constructed from overtwisted models, in terms of compaction and inter-nucleosome contacts, introducing configurational changes equivalent to those associated with 2-3 base-pair changes in nucleosome spacing. Differences in the nucleosomal DNA pathway, which underlie the way that DNA enters and exits the nucleosome, give rise to different nucleosome-decorated minicircles and affect the topological mix of configurational states.

摘要

虽然核小体是动态实体,必须经历结构变形才能发挥其功能,但从现有高分辨率结构中得到的总体观点是相对静态的。尽管已经记录了许多扭曲缺陷的例子,但围绕组蛋白核心的 DNA 通常被认为是过度扭曲的。对来自蛋白质数据库(PDB)的现有高分辨率结构的分析揭示了核小体 DNA 上扭曲的不均匀分布,存在与文献一致的明显模式,以及相当一部分的欠扭转结构。核小体 DNA 折叠的细微差异,超出了扭曲的范围,对核小体的解组装和模拟的高级结构有影响。用欠扭转模型构建的寡核小体阵列的模拟与用过度扭转模型构建的模拟非常不同,在紧凑性和核小体之间的接触方面,会产生与核小体间距中 2-3 个碱基对变化相关的构象变化。核小体 DNA 途径的差异,是 DNA 进入和离开核小体的基础,导致不同的核小体修饰的迷你环,并影响构象状态的拓扑混合。

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