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染色质在转录过程中缓冲扭转应力。

Chromatin Buffers Torsional Stress During Transcription.

作者信息

Qian Jin, Lubkowska Lucyna, Zhang Shuming, Tan Chuang, Hong Yifeng, Fulbright Robert M, Inman James T, Kay Taryn M, Jeong Joshua, Gotte Deanna, Berger James M, Kashlev Mikhail, Wang Michelle D

机构信息

Department of Physics & LASSP, Cornell University, Ithaca, NY 14853, USA.

Howard Hughes Medical Institute, Cornell University, Ithaca, NY 14853, USA.

出版信息

bioRxiv. 2024 Oct 18:2024.10.15.618270. doi: 10.1101/2024.10.15.618270.

DOI:10.1101/2024.10.15.618270
PMID:39464147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11507789/
Abstract

Transcription through chromatin under torsion represents a fundamental problem in biology. Pol II must overcome nucleosome obstacles and, because of the DNA helical structure, must also rotate relative to the DNA, generating torsional stress. However, there is a limited understanding of how Pol II transcribes through nucleosomes while supercoiling DNA. In this work, we developed methods to visualize Pol II rotation of DNA during transcription and determine how torsion slows down the transcription rate. We found that Pol II stalls at ± 9 pN·nm torque, nearly sufficient to melt DNA. The stalling is due to extensive backtracking, and the presence of TFIIS increases the stall torque to + 13 pN·nm, making Pol II a powerful rotary motor. This increased torsional capacity greatly enhances Pol II's ability to transcribe through a nucleosome. Intriguingly, when Pol II encounters a nucleosome, nucleosome passage becomes more efficient on a chromatin substrate than on a single-nucleosome substrate, demonstrating that chromatin efficiently buffers torsional stress via its torsional mechanical properties. Furthermore, topoisomerase II relaxation of torsional stress significantly enhances transcription, allowing Pol II to elongate through multiple nucleosomes. Our results demonstrate that chromatin greatly reduces torsional stress on transcription, revealing a novel role of chromatin beyond the more conventional view of it being just a roadblock to transcription.

摘要

在扭转力作用下通过染色质进行转录是生物学中的一个基本问题。RNA聚合酶II(Pol II)必须克服核小体障碍,并且由于DNA的螺旋结构,它还必须相对于DNA旋转,从而产生扭转应力。然而,对于Pol II在使DNA超螺旋的同时如何通过核小体进行转录,人们的了解还很有限。在这项工作中,我们开发了一些方法来可视化转录过程中Pol II对DNA的旋转,并确定扭转力如何降低转录速率。我们发现,Pol II在±9皮牛·纳米的扭矩下停滞,这几乎足以使DNA解链。这种停滞是由于广泛的回溯造成的,而转录延伸因子S(TFIIS)的存在将停滞扭矩增加到+13皮牛·纳米,使Pol II成为一个强大的旋转马达。这种增加的扭转能力极大地增强了Pol II通过核小体进行转录的能力。有趣的是,当Pol II遇到一个核小体时,在染色质底物上核小体的通过比在单核小体底物上更有效,这表明染色质通过其扭转力学特性有效地缓冲了扭转应力。此外,拓扑异构酶II对扭转应力的松弛显著增强了转录,使Pol II能够延伸通过多个核小体。我们的结果表明,染色质大大降低了转录过程中的扭转应力,揭示了染色质除了更传统的作为转录障碍的观点之外的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/da5949a37945/nihpp-2024.10.15.618270v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/674a41398e00/nihpp-2024.10.15.618270v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/6073917eed9e/nihpp-2024.10.15.618270v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/caa5cfa34ba4/nihpp-2024.10.15.618270v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/ead5a4e4badc/nihpp-2024.10.15.618270v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/da5949a37945/nihpp-2024.10.15.618270v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/674a41398e00/nihpp-2024.10.15.618270v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/6073917eed9e/nihpp-2024.10.15.618270v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/caa5cfa34ba4/nihpp-2024.10.15.618270v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/ead5a4e4badc/nihpp-2024.10.15.618270v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dff1/11507789/da5949a37945/nihpp-2024.10.15.618270v1-f0005.jpg

相似文献

1
Chromatin Buffers Torsional Stress During Transcription.染色质在转录过程中缓冲扭转应力。
bioRxiv. 2024 Oct 18:2024.10.15.618270. doi: 10.1101/2024.10.15.618270.
2
Transcription-generated torsional stress destabilizes nucleosomes.转录生成的扭转应力使核小体不稳定。
Nat Struct Mol Biol. 2014 Jan;21(1):88-94. doi: 10.1038/nsmb.2723. Epub 2013 Dec 8.
3
DNA torsion as a feedback mediator of transcription and chromatin dynamics.DNA扭转作为转录和染色质动力学的反馈介质。
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4
Nature of the nucleosomal barrier to RNA polymerase II.核小体对RNA聚合酶II的阻碍性质。
Mol Cell. 2005 Apr 1;18(1):97-108. doi: 10.1016/j.molcel.2005.02.027.
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Torsion is a Dynamic Regulator of DNA Replication Stalling and Reactivation.扭转是DNA复制停滞和重新激活的动态调节因子。
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Structural basis of nucleosome retention during transcription elongation.转录延伸过程中核小体保留的结构基础。
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RNA polymerase I (Pol I) passage through nucleosomes depends on Pol I subunits binding its lobe structure.RNA 聚合酶 I(Pol I)穿过核小体依赖于 Pol I 亚基与其叶状结构的结合。
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[The effect of DNA supercoiling DNA on nucleosome structure].[DNA超螺旋对核小体结构的影响]
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本文引用的文献

1
Nucleosomes play a dual role in regulating transcription dynamics.核小体在调节转录动力学方面发挥着双重作用。
Proc Natl Acad Sci U S A. 2024 Jul 9;121(28):e2319772121. doi: 10.1073/pnas.2319772121. Epub 2024 Jul 5.
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FACT maintains chromatin architecture and thereby stimulates RNA polymerase II pausing during transcription in vivo.FACT 维持染色质结构,从而在体内转录过程中刺激 RNA 聚合酶 II 暂停。
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Chromatinization modulates topoisomerase II processivity.
染色质化调节拓扑异构酶 II 的连续性。
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DNA supercoiling restricts the transcriptional bursting of neighboring eukaryotic genes.DNA 超螺旋限制了相邻真核基因的转录爆发。
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Etoposide promotes DNA loop trapping and barrier formation by topoisomerase II.依托泊苷通过拓扑异构酶 II 促进 DNA 环捕获和障碍形成。
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Structural basis of nucleosome disassembly and reassembly by RNAPII elongation complex with FACT.RNA 聚合酶 II 延伸复合物与 FACT 解组装和重新组装核小体的结构基础。
Science. 2022 Sep 9;377(6611):eabp9466. doi: 10.1126/science.abp9466. Epub 2022 Aug 18.
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Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription.补骨脂素作图揭示了转录主导的细菌基因组超螺旋景观。
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