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本文引用的文献

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Na and K Ions Differently Affect Nucleosome Structure, Stability, and Interactions with Proteins.钠离子和钾离子对核小体结构、稳定性和与蛋白质相互作用的影响不同。
Microsc Microanal. 2022 Feb;28(1):243-253. doi: 10.1017/S1431927621013751.
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Tetranucleosome Interactions Drive Chromatin Folding.四核小体相互作用驱动染色质折叠。
ACS Cent Sci. 2021 Jun 23;7(6):1019-1027. doi: 10.1021/acscentsci.1c00085. Epub 2021 May 7.
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Surprising Twists in Nucleosomal DNA with Implication for Higher-order Folding.核小体 DNA 的惊人扭曲及其对高级折叠的影响。
J Mol Biol. 2021 Sep 3;433(18):167121. doi: 10.1016/j.jmb.2021.167121. Epub 2021 Jun 28.
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The structural plasticity of nucleic acid duplexes revealed by WAXS and MD.小角X射线散射(WAXS)和分子动力学(MD)揭示的核酸双链体结构可塑性
Sci Adv. 2021 Apr 23;7(17). doi: 10.1126/sciadv.abf6106. Print 2021 Apr.
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The Dynamic Influence of Linker Histone Saturation within the Poly-Nucleosome Array.多核小体阵列中连接组蛋白饱和度的动态影响。
J Mol Biol. 2021 May 14;433(10):166902. doi: 10.1016/j.jmb.2021.166902. Epub 2021 Mar 2.
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Topological polymorphism of nucleosome fibers and folding of chromatin.核小体纤维的拓扑多态性与染色质折叠。
Biophys J. 2021 Feb 16;120(4):577-585. doi: 10.1016/j.bpj.2021.01.008. Epub 2021 Jan 16.
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How potassium came to be the dominant biological cation: of metabolism, chemiosmosis, and cation selectivity since the beginnings of life.钾元素如何成为主要的生物阳离子:自生命起源以来的代谢、化学渗透及阳离子选择性。
Bioessays. 2021 Jan;43(1):e2000108. doi: 10.1002/bies.202000108. Epub 2020 Nov 16.
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Near-atomic resolution structures of interdigitated nucleosome fibres.交错核小体纤维的近原子分辨率结构。
Nat Commun. 2020 Sep 21;11(1):4747. doi: 10.1038/s41467-020-18533-2.
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Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations.核小体-CHD4 染色质重塑器结构图谱揭示人类疾病突变。
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A dynamic view of DNA structure within the nucleosome: Biological implications.核小体中 DNA 结构的动态观点:生物学意义。
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核小体DNA的几何变化决定了高阶染色质结构以及增强子与启动子之间的通讯。

Geometric variations in nucleosomal DNA dictate higher-order chromatin structure and enhancer-promoter communication.

作者信息

Todolli Stefjord, Nizovtseva Ekaterina V, Clauvelin Nicolas, Maxian Ondrej, Studitsky Vasily M, Olson Wilma K

机构信息

Department of Chemistry and Chemical Biology, Center for Quantitative Biology, Rutgers, The State University of New Jersey, 610 Taylor Road, Piscataway, New Jersey 08854, USA.

Cancer Epigenetics Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, Pennsylvania 19422, USA.

出版信息

J Chem Phys. 2024 Dec 28;161(24). doi: 10.1063/5.0240991.

DOI:10.1063/5.0240991
PMID:39727280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11681976/
Abstract

The dynamic organization of chromatin plays an essential role in the regulation of genetic activity, interconverting between open and compact forms at the global level. The mechanisms underlying these large-scale changes remain a topic of widespread interest. The simulations of nucleosome-decorated DNA reported herein reveal profound effects of the nucleosome itself on overall chromatin properties. Models that capture the long-range communication between proteins on nucleosome-decorated DNA chains incorporate DNA pathways different from those that were previously proposed based on ultracentrifugation and chemical cross-linking data. New quantitative biochemical assays measuring the rates of communication between interacting proteins bound to a promoter and an enhancer at the ends of saturated, precisely positioned, nucleosome-decorated DNA chains reveal a chromatin architecture with a three-nucleosome repeat, a model inconsistent with the two-start configurations deduced from earlier physical studies. Accompanying computations uncover small differences in the twisting of successive base pairs that seemingly give rise to the observed global properties. These data suggest that the novel state of chromatin determined under physiological conditions differs from that deduced under standard physical conditions, likely reflecting the different salt conditions used in the two types of experiments. This novel chromatin state may be important for a number of DNA transactions that occur in the cell nucleus.

摘要

染色质的动态组织在基因活性调控中起着至关重要的作用,在全局水平上在开放和紧密形式之间相互转换。这些大规模变化背后的机制仍然是广泛关注的话题。本文报道的核小体修饰DNA的模拟揭示了核小体本身对整体染色质特性的深远影响。捕捉核小体修饰DNA链上蛋白质之间远程通讯的模型纳入了与先前基于超速离心和化学交联数据提出的不同的DNA途径。新的定量生化分析测量了结合在饱和、精确定位的核小体修饰DNA链末端的启动子和增强子上相互作用蛋白质之间的通讯速率,揭示了一种具有三个核小体重复的染色质结构,这一模型与早期物理研究推断的双起始构型不一致。伴随的计算揭示了连续碱基对扭曲的微小差异,这些差异似乎导致了观察到的全局特性。这些数据表明,在生理条件下确定的染色质新状态不同于在标准物理条件下推断的状态,这可能反映了两种类型实验中使用的不同盐条件。这种新的染色质状态可能对细胞核中发生的许多DNA交易很重要。