Evidence map›Paper›PMID 30824489›Full record

ArticleThe Journal of cell biology2019

Single nucleosome imaging reveals loose genome chromatin networks via active RNA polymerase II.

Ryosuke Nagashima, Kayo Hibino, S S Ashwin, Michael Babokhov, Shin Fujishiro, Ryosuke Imai, Tadasu Nozaki, Sachiko Tamura, Tomomi Tani, Hiroshi Kimura and 4 more

Abstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

145 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Active processes shape and move the genome and nucleoplasm.Current opinion in genetics & development · 2026
    Review
  6. Article
  7. Article
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  16. Review
  17. Article
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  19. Review
  20. Article

85 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ryosuke NagashimaGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
Kayo HibinoGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
S S AshwinDepartment of Applied Physics, Nagoya University, Nagoya, Japan.
Michael BabokhovGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
Shin FujishiroDepartment of Applied Physics, Nagoya University, Nagoya, Japan.
Ryosuke ImaiGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
Tadasu NozakiGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
Sachiko TamuraGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan.
Tomomi TaniEugene Bell Center for Regenerative Biology and Tissue Engineering, Marine Biological Laboratory, Woods Hole, MA.
Hiroshi KimuraCell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.ORCID 0000-0003-0854-083X
Michael ShribakEugene Bell Center for Regenerative Biology and Tissue Engineering, Marine Biological Laboratory, Woods Hole, MA.ORCID 0000-0002-5849-6294
Masato T KanemakiDepartment of Genetics, School of Life Science, SOKENDAI, Mishima, Japan.ORCID 0000-0002-7657-1649
Masaki SasaiDepartment of Applied Physics, Nagoya University, Nagoya, Japan.ORCID 0000-0002-1028-8242
Kazuhiro MaeshimaGenome Dynamics Laboratory, National Institute of Genetics, Research Organization of Information and Systems, Mishima, Japan kmaeshim@nig.ac.jp.ORCID 0000-0003-3909-0341

Funding

Orientation Independent DIC and Polarization MicroscopyR01GM101701 · NIGMS · MARINE BIOLOGICAL LABORATORY · PI SHRIBAK, MICHAEL · 2012 to 2020
$3.8M
NIGMS NIH HHS R01 GM101701
6 · The paper itself

Abstract

Although chromatin organization and dynamics play a critical role in gene transcription, how they interplay remains unclear. To approach this issue, we investigated genome-wide chromatin behavior under various transcriptional conditions in living human cells using single-nucleosome imaging. While transcription by RNA polymerase II (RNAPII) is generally thought to need more open and dynamic chromatin, surprisingly, we found that active RNAPII globally constrains chromatin movements. RNAPII inhibition or its rapid depletion released the chromatin constraints and increased chromatin dynamics. Perturbation experiments of P-TEFb clusters, which are associated with active RNAPII, had similar results. Furthermore, chromatin mobility also increased in resting G0 cells and UV-irradiated cells, which are transcriptionally less active. Our results demonstrated that chromatin is globally stabilized by loose connections through active RNAPII, which is compatible with models of classical transcription factories or liquid droplet formation of transcription-related factors. Together with our computational modeling, we propose the existence of loose chromatin domain networks for various intra-/interchromosomal contacts via active RNAPII clusters/droplets.

Indexed as

Transcription, GeneticCells, CulturedChromatinComputer SimulationGenome, HumanHistonesHumansImage Processing, Computer-AssistedMicroscopy, FluorescenceNucleosomesRetinal Pigment EpitheliumRNA Polymerase IIChromatinHistonesNucleosomesRNA Polymerase II

Identifiers

PMID30824489
PMCPMC6504897

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.