• 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

相分离染色质的表达依赖性折叠。

Expression-dependent folding of interphase chromatin.

机构信息

Institute for Theoretical Physics, Heidelberg, Germany.

出版信息

PLoS One. 2012;7(5):e37525. doi: 10.1371/journal.pone.0037525. Epub 2012 May 23.

DOI:10.1371/journal.pone.0037525
PMID:22649534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3359300/
Abstract

Multiple studies suggest that chromatin looping might play a crucial role in organizing eukaryotic genomes. To investigate the interplay between the conformation of interphase chromatin and its transcriptional activity, we include information from gene expression profiles into a polymer model for chromatin that incorporates genomic loops. By relating loop formation to transcriptional activity, we are able to generate chromosome conformations whose structural and topological properties are consistent with experimental data. The model particularly allows to reproduce the conformational variations that are known to occur between highly and lowly expressed chromatin regions. As previously observed in experiments, lowly expressed regions of the simulated polymers are much more compact. Due to the changes in loop formation, the distributions of chromatin loops are also expression-dependent and exhibit a steeper decay in highly active regions. As a results of entropic interaction between differently looped parts of the chromosome, we observe topological alterations leading to a preferential positioning of highly transcribed loci closer to the surface of the chromosome territory. Considering the diffusional behavior of the chromatin fibre, the simulations furthermore show that the higher the expression level of specific parts of the chromatin fibre is, the more dynamic they are. The results exhibit that variations of loop formation along the chromatin fibre, and the entropic changes that come along with it, do not only influence the structural parameters on the local scale, but also effect the global chromosome conformation and topology.

摘要

多项研究表明,染色质环可能在真核生物基因组的组织中发挥关键作用。为了研究染色质的相间构象与其转录活性之间的相互作用,我们将基因表达谱的信息纳入包含基因组环的染色质聚合物模型中。通过将环形成与转录活性相关联,我们能够生成与实验数据一致的染色体构象,其结构和拓扑性质。该模型特别允许再现已知在高表达和低表达染色质区域之间发生的构象变化。如实验中先前观察到的,模拟聚合物中低表达区域更加紧凑。由于环形成的变化,染色质环的分布也依赖于表达,并在高活性区域表现出更陡峭的衰减。由于染色体不同环部分之间的熵相互作用,我们观察到拓扑变化导致转录活跃的基因座优先定位在染色体区域的表面附近。考虑到染色质纤维的扩散行为,模拟进一步表明,特定部分的染色质纤维的表达水平越高,其动态性就越高。结果表明,沿着染色质纤维的环形成变化以及随之而来的熵变化不仅会影响局部尺度上的结构参数,还会影响全局染色体构象和拓扑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/2910bab4ecf0/pone.0037525.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/80fbbef97d26/pone.0037525.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/d9ce929adf0d/pone.0037525.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/488dd7d60e49/pone.0037525.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/f25df6691dc5/pone.0037525.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/2910bab4ecf0/pone.0037525.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/80fbbef97d26/pone.0037525.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/d9ce929adf0d/pone.0037525.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/488dd7d60e49/pone.0037525.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/f25df6691dc5/pone.0037525.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa3d/3359300/2910bab4ecf0/pone.0037525.g005.jpg

相似文献

1
Expression-dependent folding of interphase chromatin.相分离染色质的表达依赖性折叠。
PLoS One. 2012;7(5):e37525. doi: 10.1371/journal.pone.0037525. Epub 2012 May 23.
2
Simulation of Different Three-Dimensional Models of Whole Interphase Nuclei Compared to Experiments - A Consistent Scale-Bridging Simulation Framework for Genome Organization.模拟全相间核的不同三维模型与实验比较——基因组组织的一致的跨尺度模拟框架。
Results Probl Cell Differ. 2022;70:495-549. doi: 10.1007/978-3-031-06573-6_18.
3
Simulation of different three-dimensional polymer models of interphase chromosomes compared to experiments-an evaluation and review framework of the 3D genome organization.模拟不同的相间染色体的三维聚合物模型与实验比较——3D 基因组组织的评估和综述框架。
Semin Cell Dev Biol. 2019 Jun;90:19-42. doi: 10.1016/j.semcdb.2018.07.012. Epub 2018 Aug 24.
4
Entropic organization of interphase chromosomes.间期染色体的熵组织
J Cell Biol. 2009 Sep 21;186(6):825-34. doi: 10.1083/jcb.200903083. Epub 2009 Sep 14.
5
Chromatin folding--from biology to polymer models and back.染色质折叠——从生物学到聚合物模型再到生物学。
J Cell Sci. 2011 Mar 15;124(Pt 6):839-45. doi: 10.1242/jcs.077628.
6
Diffusion-driven looping provides a consistent framework for chromatin organization.扩散驱动的环化提供了一个一致的染色质组织框架。
PLoS One. 2010 Aug 25;5(8):e12218. doi: 10.1371/journal.pone.0012218.
7
[Topology of chromosomes in somatic cells. Part 1].[体细胞中染色体的拓扑结构。第1部分]
Postepy Hig Med Dosw (Online). 2006;60:331-42.
8
Spatially confined folding of chromatin in the interphase nucleus.间期细胞核中染色质的空间受限折叠
Proc Natl Acad Sci U S A. 2009 Mar 10;106(10):3812-7. doi: 10.1073/pnas.0809501106. Epub 2009 Feb 20.
9
Looping probabilities in model interphase chromosomes.模型相间染色体中的环化概率。
Biophys J. 2010 Jun 2;98(11):2410-9. doi: 10.1016/j.bpj.2010.01.054.
10
The Physical Behavior of Interphase Chromosomes: Polymer Theory and Coarse-Grain Computer Simulations.染色质的物理行为:高分子理论与粗粒化计算机模拟。
Methods Mol Biol. 2022;2301:235-258. doi: 10.1007/978-1-0716-1390-0_12.

引用本文的文献

1
A guide to studying 3D genome structure and dynamics in the kidney.肾脏三维基因组结构与动力学研究指南。
Nat Rev Nephrol. 2025 Feb;21(2):97-114. doi: 10.1038/s41581-024-00894-2. Epub 2024 Oct 15.
2
Consistencies and contradictions in different polymer models of chromatin architecture.染色质结构不同聚合物模型中的一致性与矛盾之处。
Comput Struct Biotechnol J. 2023 Jan 24;21:1084-1091. doi: 10.1016/j.csbj.2023.01.033. eCollection 2023.
3
Mechanisms of Chromosome Folding and Nuclear Organization: Their Interplay and Open Questions.

本文引用的文献

1
The fractal globule as a model of chromatin architecture in the cell.作为细胞中染色质结构模型的分形球。
Chromosome Res. 2011 Jan;19(1):37-51. doi: 10.1007/s10577-010-9177-0.
2
Repulsive forces between looping chromosomes induce entropy-driven segregation.染色体环之间的斥力诱导了熵驱动的分离。
PLoS One. 2011 Jan 4;6(1):e14428. doi: 10.1371/journal.pone.0014428.
3
Diffusion-driven looping provides a consistent framework for chromatin organization.扩散驱动的环化提供了一个一致的染色质组织框架。
染色体折叠和核组织的机制:它们的相互作用和未解决的问题。
Cold Spring Harb Perspect Biol. 2022 Jul 1;14(7):a040147. doi: 10.1101/cshperspect.a040147.
4
Computational 3D genome modeling using Chrom3D.使用 Chrom3D 进行计算三维基因组建模。
Nat Protoc. 2018 May;13(5):1137-1152. doi: 10.1038/nprot.2018.009. Epub 2018 Apr 26.
5
Transient chromatin properties revealed by polymer models and stochastic simulations constructed from Chromosomal Capture data.由聚合物模型和基于染色体捕获数据构建的随机模拟揭示的瞬时染色质特性。
PLoS Comput Biol. 2017 Apr 3;13(4):e1005469. doi: 10.1371/journal.pcbi.1005469. eCollection 2017 Apr.
6
Perspectives: using polymer modeling to understand the formation and function of nuclear compartments.观点:利用聚合物建模来理解核区室的形成与功能
Chromosome Res. 2017 Mar;25(1):35-50. doi: 10.1007/s10577-016-9548-2. Epub 2017 Jan 14.
7
Quantified effects of chromosome-nuclear envelope attachments on 3D organization of chromosomes.染色体与核膜附着对染色体三维组织的量化影响。
Nucleus. 2015;6(3):212-24. doi: 10.1080/19491034.2015.1056441.
8
Radiation induced chromatin conformation changes analysed by fluorescent localization microscopy, statistical physics, and graph theory.通过荧光定位显微镜、统计物理学和图论分析辐射诱导的染色质构象变化。
PLoS One. 2015 Jun 4;10(6):e0128555. doi: 10.1371/journal.pone.0128555. eCollection 2015.
9
Depletion of the chromatin looping proteins CTCF and cohesin causes chromatin compaction: insight into chromatin folding by polymer modelling.染色质环化蛋白CTCF和黏连蛋白的缺失会导致染色质压缩:通过聚合物建模深入了解染色质折叠。
PLoS Comput Biol. 2014 Oct 9;10(10):e1003877. doi: 10.1371/journal.pcbi.1003877. eCollection 2014 Oct.
10
Modeling epigenome folding: formation and dynamics of topologically associated chromatin domains.表观基因组折叠建模:拓扑相关染色质结构域的形成与动态变化
Nucleic Acids Res. 2014 Sep;42(15):9553-61. doi: 10.1093/nar/gku698. Epub 2014 Aug 4.
PLoS One. 2010 Aug 25;5(8):e12218. doi: 10.1371/journal.pone.0012218.
4
Chromatin structure: does the 30-nm fibre exist in vivo?染色质结构:30nm 纤维是否存在于体内?
Curr Opin Cell Biol. 2010 Jun;22(3):291-7. doi: 10.1016/j.ceb.2010.03.001. Epub 2010 Mar 24.
5
Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells.共调控基因之间的优先关联揭示了红细胞中的转录互作网络。
Nat Genet. 2010 Jan;42(1):53-61. doi: 10.1038/ng.496. Epub 2009 Dec 13.
6
Comprehensive mapping of long-range interactions reveals folding principles of the human genome.远距离相互作用的全面图谱揭示了人类基因组的折叠原理。
Science. 2009 Oct 9;326(5950):289-93. doi: 10.1126/science.1181369.
7
Entropic organization of interphase chromosomes.间期染色体的熵组织
J Cell Biol. 2009 Sep 21;186(6):825-34. doi: 10.1083/jcb.200903083. Epub 2009 Sep 14.
8
Topological origins of chromosomal territories.染色体领地的拓扑起源。
Nucleic Acids Res. 2009 Oct;37(19):6316-22. doi: 10.1093/nar/gkp702. Epub 2009 Sep 2.
9
Chromosome conformation capture (from 3C to 5C) and its ChIP-based modification.染色体构象捕获技术(从3C到5C)及其基于染色质免疫沉淀的修饰。
Methods Mol Biol. 2009;567:171-88. doi: 10.1007/978-1-60327-414-2_12.
10
Non-specific interactions are sufficient to explain the position of heterochromatic chromocenters and nucleoli in interphase nuclei.非特异性相互作用足以解释异染色质染色中心和核仁在间期细胞核中的位置。
Nucleic Acids Res. 2009 Jun;37(11):3558-68. doi: 10.1093/nar/gkp219. Epub 2009 Apr 9.