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Linker histone H1.8 inhibits chromatin binding of condensins and DNA topoisomerase II to tune chromosome length and individualization.连接组蛋白 H1.8 抑制凝聚素和 DNA 拓扑异构酶 II 与染色质的结合,以调节染色体长度和个体化。
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Topoisomerase II does not play a scaffolding role in the organization of mitotic chromosomes assembled in Xenopus egg extracts.拓扑异构酶II在非洲爪蟾卵提取物中组装的有丝分裂染色体的组织过程中不发挥支架作用。
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引用本文的文献

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Elasticity control of entangled chromosomes: Crosstalk between condensin complexes and nucleosomes.纠缠染色体的弹性控制:凝聚复合物和核小体之间的串扰。
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本文引用的文献

1
Linker histone H1.8 inhibits chromatin binding of condensins and DNA topoisomerase II to tune chromosome length and individualization.连接组蛋白 H1.8 抑制凝聚素和 DNA 拓扑异构酶 II 与染色质的结合,以调节染色体长度和个体化。
Elife. 2021 Aug 18;10:e68918. doi: 10.7554/eLife.68918.
2
Guiding functions of the C-terminal domain of topoisomerase IIα advance mitotic chromosome assembly.拓扑异构酶 IIα 的 C 末端结构域的引导功能促进有丝分裂染色体的组装。
Nat Commun. 2021 May 18;12(1):2917. doi: 10.1038/s41467-021-23205-w.
3
Mitotic chromosomes.有丝分裂染色体。
Semin Cell Dev Biol. 2021 Sep;117:7-29. doi: 10.1016/j.semcdb.2021.03.014. Epub 2021 Apr 6.
4
Human Condensin I and II Drive Extensive ATP-Dependent Compaction of Nucleosome-Bound DNA.人源凝聚素 I 和 II 驱动核小体结合 DNA 的广泛 ATP 依赖性紧缩。
Mol Cell. 2020 Jul 2;79(1):99-114.e9. doi: 10.1016/j.molcel.2020.04.026. Epub 2020 May 22.
5
Cohesin and condensin extrude DNA loops in a cell cycle-dependent manner.黏合蛋白和凝聚蛋白以细胞周期依赖性的方式挤出 DNA 环。
Elife. 2020 May 12;9:e53885. doi: 10.7554/eLife.53885.
6
Chromosome disentanglement driven via optimal compaction of loop-extruded brush structures.通过最优压缩环伸出刷状结构驱动染色体解缠。
Proc Natl Acad Sci U S A. 2019 Dec 10;116(50):24956-24965. doi: 10.1073/pnas.1906355116. Epub 2019 Nov 22.
7
Organization of Chromatin by Intrinsic and Regulated Phase Separation.染色质的固有和调控相分离组织。
Cell. 2019 Oct 3;179(2):470-484.e21. doi: 10.1016/j.cell.2019.08.037. Epub 2019 Sep 19.
8
Retardation of the reaction kinetics of polymers due to entanglement in the post-gel stage in multi-chain slip-spring simulations.多链滑移弹簧模拟中后凝胶阶段聚合物缠结对反应动力学的迟缓作用。
Soft Matter. 2019 Jun 26;15(25):5109-5115. doi: 10.1039/c9sm00681h.
9
Highly disordered histone H1-DNA model complexes and their condensates.高度无序的组蛋白 H1-DNA 模型复合物及其凝聚体。
Proc Natl Acad Sci U S A. 2018 Nov 20;115(47):11964-11969. doi: 10.1073/pnas.1805943115. Epub 2018 Oct 9.
10
Real-time imaging of DNA loop extrusion by condensin.凝缩蛋白介导的DNA环挤压的实时成像
Science. 2018 Apr 6;360(6384):102-105. doi: 10.1126/science.aar7831. Epub 2018 Feb 22.

环挤出驱动缠结染色体的体积相转变。

Loop extrusion driven volume phase transition of entangled chromosomes.

机构信息

Institute for Chemical Reaction Design and Discovery, Hokkaido University, Sapporo, Japan.

Cluster of Excellence Physics of Life, TU Dresden, Dresden, Germany.

出版信息

Biophys J. 2022 Jul 19;121(14):2742-2750. doi: 10.1016/j.bpj.2022.06.014. Epub 2022 Jun 15.

DOI:10.1016/j.bpj.2022.06.014
PMID:35706364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9382337/
Abstract

Experiments on reconstituted chromosomes have revealed that mitotic chromosomes are assembled even without nucleosomes. When topoisomerase II (topo II) is depleted from such reconstituted chromosomes, these chromosomes are not disentangled and form "sparklers," where DNA and linker histone are condensed in the core and condensin is localized at the periphery. To understand the mechanism of the assembly of sparklers, we here take into account the loop extrusion by condensin in an extension of the theory of entangled polymer gels. The loop extrusion stiffens an entangled DNA network because DNA segments in the elastically effective chains are translocated to loops, which are elastically ineffective. Our theory predicts that the loop extrusion by condensin drives the volume phase transition that collapses a swollen entangled DNA gel because the stiffening of the network destabilizes the swollen phase. This may be an important piece to understand the mechanism of the assembly of mitotic chromosomes.

摘要

重构染色体的实验表明,即使没有核小体,有丝分裂染色体也能组装。当拓扑异构酶 II (topo II) 从这种重构的染色体中耗尽时,这些染色体不会解开并形成“烟花”,其中 DNA 和连接组蛋白在核心中浓缩,凝聚蛋白位于外围。为了理解烟花形成的机制,我们在这里考虑了凝聚蛋白在纠缠聚合物凝胶理论延伸中的环挤出。环挤出使纠缠的 DNA 网络变硬,因为弹性有效链中的 DNA 片段被转移到环中,而环是无弹性的。我们的理论预测,凝聚蛋白的环挤出驱动了体积相转变,使肿胀的纠缠 DNA 凝胶坍塌,因为网络的变硬使肿胀相不稳定。这可能是理解有丝分裂染色体组装机制的重要一环。