• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

局部体积浓度、包装域和染色质的缩放性质。

Local volume concentration, packing domains, and scaling properties of chromatin.

机构信息

Department of Biomedical Engineering, Northwestern University, Evanston, United States.

Magnetism and Interface Physics & Computational Polymer Physics, Department of Materials, ETH Zurich, Zurich, Switzerland.

出版信息

Elife. 2024 Sep 27;13:RP97604. doi: 10.7554/eLife.97604.

DOI:10.7554/eLife.97604
PMID:39331520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11434620/
Abstract

We propose the Self Returning Excluded Volume (SR-EV) model for the structure of chromatin based on stochastic rules and physical interactions. The SR-EV generate conformationally defined domains observed by single-cell imaging techniques. From nucleosome to chromosome scales, the model captures the overall chromatin organization as a corrugated system, with dense and dilute regions alternating in a manner that resembles the mixing of two disordered bi-continuous phases. This particular organizational topology is a consequence of the multiplicity of interactions and processes occurring in the nuclei, and mimicked by the proposed return rules. Single configuration properties and ensemble averages show a robust agreement between theoretical and experimental results including chromatin volume concentration, contact probability, packing domain identification and size characterization, and packing scaling behavior. Model and experimental results suggest that there is an inherent chromatin organization regardless of the cell character and resistant to an external forcing such as RAD21 degradation.

摘要

我们提出了基于随机规则和物理相互作用的染色质结构的自归巢排斥体积 (SR-EV) 模型。SR-EV 产生通过单细胞成像技术观察到的构象定义的域。从核小体到染色体尺度,该模型将整体染色质组织捕获为波纹系统,密集和稀疏区域以类似于两种无序双连续相混合的方式交替。这种特殊的组织拓扑结构是核内发生的多种相互作用和过程的结果,并通过提出的返回规则来模拟。单个构型特性和整体平均值表明理论和实验结果之间存在稳健的一致性,包括染色质体积浓度、接触概率、包装域识别和大小特征以及包装缩放行为。模型和实验结果表明,存在内在的染色质组织,无论细胞特征如何,并且不受 RAD21 降解等外部强制的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/60a04fd53241/elife-97604-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/9bcd0c8924be/elife-97604-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7be7648b2528/elife-97604-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7e70317776be/elife-97604-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/6f9b1dd307ce/elife-97604-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/279b82560adc/elife-97604-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/8518b2320954/elife-97604-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/09a3809c880d/elife-97604-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7bab102bd93b/elife-97604-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/ccd5ea98559a/elife-97604-fig7-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/d204001c2c71/elife-97604-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/d45975bb385c/elife-97604-fig8-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/ac6d82deb9e2/elife-97604-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/60a04fd53241/elife-97604-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/9bcd0c8924be/elife-97604-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7be7648b2528/elife-97604-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7e70317776be/elife-97604-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/6f9b1dd307ce/elife-97604-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/279b82560adc/elife-97604-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/8518b2320954/elife-97604-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/09a3809c880d/elife-97604-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/7bab102bd93b/elife-97604-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/ccd5ea98559a/elife-97604-fig7-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/d204001c2c71/elife-97604-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/d45975bb385c/elife-97604-fig8-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/ac6d82deb9e2/elife-97604-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/770e/11434620/60a04fd53241/elife-97604-fig10.jpg

相似文献

1
Local volume concentration, packing domains, and scaling properties of chromatin.局部体积浓度、包装域和染色质的缩放性质。
Elife. 2024 Sep 27;13:RP97604. doi: 10.7554/eLife.97604.
2
Local Volume Concentration, Packing Domains and Scaling Properties of Chromatin.染色质的局部体积浓度、堆积结构域和标度性质
ArXiv. 2024 Jun 13:arXiv:2310.02257v3.
3
Local Volume Concentration, Packing Domains and Scaling Properties of Chromatin.染色质的局部体积浓度、堆积结构域和标度性质
Res Sq. 2023 Oct 17:rs.3.rs-3399177. doi: 10.21203/rs.3.rs-3399177/v1.
4
Macromolecular crowding: chemistry and physics meet biology (Ascona, Switzerland, 10-14 June 2012).大分子拥挤现象:化学与物理邂逅生物学(瑞士阿斯科纳,2012年6月10日至14日)
Phys Biol. 2013 Aug;10(4):040301. doi: 10.1088/1478-3975/10/4/040301. Epub 2013 Aug 2.
5
[Attraction of Likenesses: Mechanisms of Self-Association and Compartmentalization of Eukaryotic Chromatin].[相似性的吸引:真核染色质的自我关联和区室化机制]
Mol Biol (Mosk). 2019 Nov-Dec;53(6):933-953. doi: 10.1134/S0026898419060053.
6
DNA topology in chromatin is defined by nucleosome spacing.染色质中的 DNA 拓扑结构由核小体间隔定义。
Sci Adv. 2017 Oct 27;3(10):e1700957. doi: 10.1126/sciadv.1700957. eCollection 2017 Oct.
7
A variable topology for the 30-nm chromatin fibre.30纳米染色质纤维的可变拓扑结构。
EMBO Rep. 2007 Dec;8(12):1129-34. doi: 10.1038/sj.embor.7401115.
8
Organization of fast and slow chromatin revealed by single-nucleosome dynamics.通过单个核小体动力学揭示快速和慢速染色质的组织。
Proc Natl Acad Sci U S A. 2019 Oct 1;116(40):19939-19944. doi: 10.1073/pnas.1907342116. Epub 2019 Sep 16.
9
From Nucleosomes to Compartments: Physicochemical Interactions Underlying Chromatin Organization.从核小体到区室:染色质组织的物理化学相互作用。
Annu Rev Biophys. 2024 Jul;53(1):221-245. doi: 10.1146/annurev-biophys-030822-032650. Epub 2024 Jun 28.
10
Capturing Structural Heterogeneity in Chromatin Fibers.捕捉染色质纤维中的结构异质性。
J Mol Biol. 2017 Oct 13;429(20):3031-3042. doi: 10.1016/j.jmb.2017.09.002. Epub 2017 Sep 9.

引用本文的文献

1
Multiplexed Chromatin Analysis Using Optical Spectroscopic Statistical Nanosensing.利用光谱统计纳米传感技术进行多重染色质分析
ACS Photonics. 2025 Jul 10. doi: 10.1021/acsphotonics.5c00311.
2
Geometrically encoded positioning of introns, intergenic segments, and exons in the human genome.人类基因组中内含子、基因间区域和外显子的几何编码定位
bioRxiv. 2025 May 29:2025.05.29.656862. doi: 10.1101/2025.05.29.656862.
3
Chromatin conformation, gene transcription, and nucleosome remodeling as an emergent system.染色质构象、基因转录和核小体重塑作为一个涌现系统。

本文引用的文献

1
In vitro reconstitution of chromatin domains shows a role for nucleosome positioning in 3D genome organization.体外重建染色质结构域表明核小体定位在 3D 基因组组织中的作用。
Nat Genet. 2024 Mar;56(3):483-492. doi: 10.1038/s41588-023-01649-8. Epub 2024 Jan 30.
2
Transcription modulates chromatin dynamics and locus configuration sampling.转录调节染色质动力学和基因座构象采样。
Nat Struct Mol Biol. 2023 Sep;30(9):1275-1285. doi: 10.1038/s41594-023-01059-8. Epub 2023 Aug 3.
3
Regulation of chromatin microphase separation by binding of protein complexes.
Sci Adv. 2025 Jan 10;11(2):eadq6652. doi: 10.1126/sciadv.adq6652.
通过蛋白质复合物的结合调控染色质微分离相
Elife. 2023 Jul 12;12:e82983. doi: 10.7554/eLife.82983.
4
Theory of chromatin organization maintained by active loop extrusion.由活跃的环挤出维持的染色质组织理论。
Proc Natl Acad Sci U S A. 2023 Jun 6;120(23):e2222078120. doi: 10.1073/pnas.2222078120. Epub 2023 May 30.
5
Topologically associating domain boundaries are required for normal genome function.拓扑关联域边界对于正常的基因组功能是必需的。
Commun Biol. 2023 Apr 20;6(1):435. doi: 10.1038/s42003-023-04819-w.
6
Chromatin accessibility: methods, mechanisms, and biological insights.染色质可及性:方法、机制与生物学见解。
Nucleus. 2022 Dec;13(1):236-276. doi: 10.1080/19491034.2022.2143106.
7
Chromatin Liquid-Liquid Phase Separation (LLPS) Is Regulated by Ionic Conditions and Fiber Length.染色质液-液相分离(LLPS)受离子条件和纤维长度的调节。
Cells. 2022 Oct 6;11(19):3145. doi: 10.3390/cells11193145.
8
CTCF-CTCF loops and intra-TAD interactions show differential dependence on cohesin ring integrity.CTCF-CTCF 环和 intra-TAD 相互作用显示出对黏连蛋白环完整性的不同依赖性。
Nat Cell Biol. 2022 Oct;24(10):1516-1527. doi: 10.1038/s41556-022-00992-y. Epub 2022 Oct 6.
9
Brownian dynamics simulations of mesoscale chromatin fibers.介观染色质纤维的布朗动力学模拟。
Biophys J. 2023 Jul 25;122(14):2884-2897. doi: 10.1016/j.bpj.2022.09.013. Epub 2022 Sep 17.
10
Analysis of three-dimensional chromatin packing domains by chromatin scanning transmission electron microscopy (ChromSTEM).通过染色质扫描透射电子显微镜(ChromSTEM)分析三维染色质包装域。
Sci Rep. 2022 Jul 16;12(1):12198. doi: 10.1038/s41598-022-16028-2.