• 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

复制体加载可减少染色质运动,而与 DNA 合成无关。

Replisome loading reduces chromatin motion independent of DNA synthesis.

机构信息

Department of Biology, Technical University of Darmstadt, Darmstadt, Germany.

Biomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Heidelberg, Germany.

出版信息

Elife. 2023 Oct 31;12:RP87572. doi: 10.7554/eLife.87572.

DOI:10.7554/eLife.87572
PMID:37906089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10617993/
Abstract

Chromatin has been shown to undergo diffusional motion, which is affected during gene transcription by RNA polymerase activity. However, the relationship between chromatin mobility and other genomic processes remains unclear. Hence, we set out to label the DNA directly in a sequence unbiased manner and followed labeled chromatin dynamics in interphase human cells expressing GFP-tagged proliferating cell nuclear antigen (PCNA), a cell cycle marker and core component of the DNA replication machinery. We detected decreased chromatin mobility during the S-phase compared to G1 and G2 phases in tumor as well as normal diploid cells using automated particle tracking. To gain insight into the dynamical organization of the genome during DNA replication, we determined labeled chromatin domain sizes and analyzed their motion in replicating cells. By correlating chromatin mobility proximal to the active sites of DNA synthesis, we showed that chromatin motion was locally constrained at the sites of DNA replication. Furthermore, inhibiting DNA synthesis led to increased loading of DNA polymerases. This was accompanied by accumulation of the single-stranded DNA binding protein on the chromatin and activation of DNA helicases further restricting local chromatin motion. We, therefore, propose that it is the loading of replisomes but not their catalytic activity that reduces the dynamics of replicating chromatin segments in the S-phase as well as their accessibility and probability of interactions with other genomic regions.

摘要

染色质已被证明会发生扩散运动,这种运动在基因转录过程中会受到 RNA 聚合酶活性的影响。然而,染色质流动性与其他基因组过程之间的关系尚不清楚。因此,我们着手以非序列偏向的方式直接标记 DNA,并在表达 GFP 标记的增殖细胞核抗原(PCNA)的人间期细胞中追踪标记的染色质动力学,PCNA 是细胞周期标志物和 DNA 复制机制的核心组成部分。我们使用自动粒子追踪技术检测到,与 G1 和 G2 期相比,肿瘤和正常二倍体细胞在 S 期的染色质流动性降低。为了深入了解 DNA 复制过程中基因组的动态组织,我们确定了标记染色质结构域的大小,并分析了它们在复制细胞中的运动。通过将靠近 DNA 合成活性位点的染色质流动性进行关联,我们表明在 DNA 复制位点处染色质运动受到局部限制。此外,抑制 DNA 合成会导致 DNA 聚合酶的加载增加。这伴随着单链 DNA 结合蛋白在染色质上的积累以及 DNA 解旋酶的激活,进一步限制了局部染色质运动。因此,我们提出正是复制体的加载而不是它们的催化活性降低了 S 期复制染色质片段的动力学以及它们与其他基因组区域相互作用的可及性和概率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/3ae0db3b71bb/elife-87572-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/58f27abfe1aa/elife-87572-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/17bccea93d23/elife-87572-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/a7169f33b0dc/elife-87572-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/41f1cb919151/elife-87572-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/43a2545a36e2/elife-87572-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/c3705bc5a07d/elife-87572-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/b5eb3568bd26/elife-87572-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/928460e78d3a/elife-87572-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/d904bcb42e9a/elife-87572-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/410ec6ba609a/elife-87572-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/c779822823cf/elife-87572-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/fe56cdad7484/elife-87572-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/f2c80dfb377b/elife-87572-fig5-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/1372a9927baa/elife-87572-fig5-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/bbbdba7001bb/elife-87572-fig5-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/b36bff67cdf1/elife-87572-fig5-figsupp8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/ed61173f689a/elife-87572-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/7fa25e5c3743/elife-87572-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/3ae0db3b71bb/elife-87572-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/58f27abfe1aa/elife-87572-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/17bccea93d23/elife-87572-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/a7169f33b0dc/elife-87572-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/41f1cb919151/elife-87572-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/43a2545a36e2/elife-87572-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/c3705bc5a07d/elife-87572-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/b5eb3568bd26/elife-87572-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/928460e78d3a/elife-87572-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/d904bcb42e9a/elife-87572-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/410ec6ba609a/elife-87572-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/c779822823cf/elife-87572-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/fe56cdad7484/elife-87572-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/f2c80dfb377b/elife-87572-fig5-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/1372a9927baa/elife-87572-fig5-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/bbbdba7001bb/elife-87572-fig5-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/b36bff67cdf1/elife-87572-fig5-figsupp8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/ed61173f689a/elife-87572-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/7fa25e5c3743/elife-87572-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44fb/10617993/3ae0db3b71bb/elife-87572-fig6-figsupp2.jpg

相似文献

1
Replisome loading reduces chromatin motion independent of DNA synthesis.复制体加载可减少染色质运动,而与 DNA 合成无关。
Elife. 2023 Oct 31;12:RP87572. doi: 10.7554/eLife.87572.
2
PCNA is recruited to irradiated chromatin in late S-phase and is most pronounced in G2 phase of the cell cycle.增殖细胞核抗原(PCNA)在S期晚期被募集到受辐射的染色质上,在细胞周期的G2期最为明显。
Protoplasma. 2017 Sep;254(5):2035-2043. doi: 10.1007/s00709-017-1076-1. Epub 2017 Jan 20.
3
Human replication proteins hCdc21, hCdc46 and P1Mcm3 bind chromatin uniformly before S-phase and are displaced locally during DNA replication.人类复制蛋白hCdc21、hCdc46和P1Mcm3在S期之前均匀地结合染色质,并在DNA复制过程中局部移位。
J Cell Sci. 1996 Feb;109 ( Pt 2):309-18. doi: 10.1242/jcs.109.2.309.
4
Dynamic changes in subnuclear NP95 location during the cell cycle and its spatial relationship with DNA replication foci.细胞周期中核内亚核NP95位置的动态变化及其与DNA复制位点的空间关系。
Exp Cell Res. 2001 Feb 15;263(2):202-8. doi: 10.1006/excr.2000.5115.
5
DNA choreography: correlating mobility and organization of DNA across different resolutions from loops to chromosomes.DNA 舞蹈编排:将 DNA 的运动性和组织性关联起来,从环到染色体,跨越不同分辨率。
Histochem Cell Biol. 2024 Jul;162(1-2):109-131. doi: 10.1007/s00418-024-02285-x. Epub 2024 May 17.
6
p21CDKN1A does not interfere with loading of PCNA at DNA replication sites, but inhibits subsequent binding of DNA polymerase delta at the G1/S phase transition.p21CDKN1A并不干扰增殖细胞核抗原(PCNA)在DNA复制位点的加载,但会在G1/S期转换时抑制DNA聚合酶δ的后续结合。
Cell Cycle. 2003 Nov-Dec;2(6):596-603.
7
Chromosome Duplication in Saccharomyces cerevisiae.酿酒酵母中的染色体复制
Genetics. 2016 Jul;203(3):1027-67. doi: 10.1534/genetics.115.186452.
8
ATAD5 regulates the lifespan of DNA replication factories by modulating PCNA level on the chromatin.ATAD5 通过调节染色质上 PCNA 的水平来调控 DNA 复制工厂的寿命。
J Cell Biol. 2013 Jan 7;200(1):31-44. doi: 10.1083/jcb.201206084. Epub 2012 Dec 31.
9
Pfh1 Is an Accessory Replicative Helicase that Interacts with the Replisome to Facilitate Fork Progression and Preserve Genome Integrity.Pfh1是一种辅助性复制解旋酶,它与复制体相互作用以促进叉状结构的进展并维持基因组完整性。
PLoS Genet. 2016 Sep 9;12(9):e1006238. doi: 10.1371/journal.pgen.1006238. eCollection 2016 Sep.
10
Replication sites as revealed by double label immunofluorescence against proliferating cell nuclear antigen (PCNA) and bromodeoxyuridine (BrdU) in synchronized CHO cells and vincristine-induced multinucleate cells.通过对同步化的中国仓鼠卵巢(CHO)细胞和长春新碱诱导的多核细胞进行增殖细胞核抗原(PCNA)和溴脱氧尿苷(BrdU)的双重标记免疫荧光所揭示的复制位点。
Biol Cell. 1994;82(1):23-31. doi: 10.1016/0248-4900(94)90062-0.

引用本文的文献

1
Transcriptional activity generates chromatin motion that drives nuclear blebbing.转录活性产生染色质运动,进而驱动核泡化。
bioRxiv. 2025 May 21:2025.05.20.655131. doi: 10.1101/2025.05.20.655131.
2
DNA choreography: correlating mobility and organization of DNA across different resolutions from loops to chromosomes.DNA 舞蹈编排:将 DNA 的运动性和组织性关联起来,从环到染色体,跨越不同分辨率。
Histochem Cell Biol. 2024 Jul;162(1-2):109-131. doi: 10.1007/s00418-024-02285-x. Epub 2024 May 17.
3
Timeless-Tipin interactions with MCM and RPA mediate DNA replication stress response.

本文引用的文献

1
Cohesin and CTCF control the dynamics of chromosome folding.黏合蛋白和 CTCF 控制着染色体折叠的动态变化。
Nat Genet. 2022 Dec;54(12):1907-1918. doi: 10.1038/s41588-022-01232-7. Epub 2022 Dec 5.
2
Effects of Transcription-Dependent Physical Perturbations on the Chromosome Dynamics in Living Cells.转录依赖性物理扰动对活细胞染色体动力学的影响。
Front Cell Dev Biol. 2022 Jul 7;10:822026. doi: 10.3389/fcell.2022.822026. eCollection 2022.
3
A Liquid State Perspective on Dynamics of Chromatin Compartments.染色质区室动力学的液态视角
Timeless与Tipin和MCM以及RPA的相互作用介导DNA复制应激反应。
Front Cell Dev Biol. 2024 Feb 29;12:1346534. doi: 10.3389/fcell.2024.1346534. eCollection 2024.
Front Mol Biosci. 2022 Jan 13;8:781981. doi: 10.3389/fmolb.2021.781981. eCollection 2021.
4
Live imaging of transcription sites using an elongating RNA polymerase II-specific probe.使用延伸中的 RNA 聚合酶 II 特异性探针进行转录位点的活体成像。
J Cell Biol. 2022 Feb 7;221(2). doi: 10.1083/jcb.202104134. Epub 2021 Dec 2.
5
Precise measurements of chromatin diffusion dynamics by modeling using Gaussian processes.通过使用高斯过程建模对染色质扩散动力学进行精确测量。
Nat Commun. 2021 Oct 26;12(1):6184. doi: 10.1038/s41467-021-26466-7.
6
Isolation of Chromatin-bound Proteins from Subcellular Fractions for Biochemical Analysis.从亚细胞组分中分离染色质结合蛋白用于生化分析。
Bio Protoc. 2018 Oct 5;8(19):e3035. doi: 10.21769/BioProtoc.3035.
7
Data fusion and smoothing for probabilistic tracking of viral structures in fluorescence microscopy images.荧光显微镜图像中病毒结构的概率跟踪的数据融合与平滑。
Med Image Anal. 2021 Oct;73:102168. doi: 10.1016/j.media.2021.102168. Epub 2021 Jul 16.
8
Biomolecular condensates at sites of DNA damage: More than just a phase.生物分子凝聚物在 DNA 损伤部位:不仅仅是一个阶段。
DNA Repair (Amst). 2021 Oct;106:103179. doi: 10.1016/j.dnarep.2021.103179. Epub 2021 Jul 14.
9
Polymer models are a versatile tool to study chromatin 3D organization.聚合物模型是研究染色质三维结构的一种通用工具。
Biochem Soc Trans. 2021 Aug 27;49(4):1675-1684. doi: 10.1042/BST20201004.
10
Cytosine base modifications regulate DNA duplex stability and metabolism.胞嘧啶碱基修饰调节 DNA 双链稳定性和代谢。
Nucleic Acids Res. 2021 Dec 16;49(22):12870-12894. doi: 10.1093/nar/gkab509.