Evidence map›Paper›PMID 31952809›Full record

ArticleBiophysical journal2020

Structural Studies of Overlapping Dinucleosomes in Solution.

Atsushi Matsumoto, Masaaki Sugiyama, Zhenhai Li, Anne Martel, Lionel Porcar, Rintaro Inoue, Daiki Kato, Akihisa Osakabe, Hitoshi Kurumizaka, Hidetoshi Kono

Open access · hybridAbstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Structural studies of functional nucleosome complexes with transacting factors.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Review
  14. Article
  15. Deuteration Aiming for Neutron Scattering.Biophysics and physicobiology · 2021
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Atsushi MatsumotoInstitute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan.
Masaaki SugiyamaInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Japan. Electronic address: sugiyama@rri.kyoto-u.ac.jp.
Zhenhai LiInstitute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan.
Anne MartelInstitut Laue-Langevin, Grenoble, France.
Lionel PorcarInstitut Laue-Langevin, Grenoble, France.
Rintaro InoueInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Japan.
Daiki KatoGraduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
Akihisa OsakabeGraduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
Hitoshi KurumizakaGraduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan; Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences, The University of Tokyo, Tokyo, Japan. Electronic address: kurumizaka@iam.u-tokyo.ac.jp.
Hidetoshi KonoInstitute for Quantum Life Science, National Institutes for Quantum and Radiological Science and Technology, Kizugawa, Japan. Electronic address: kono.hidetoshi@qst.go.jp.
National Institutes for Quantum Science and Technology · JPWaseda University · JPInstitut Laue-Langevin · FRKyoto University · JP

Funding

Austrian Science Fund FWF M 2539
6 · The paper itself

Abstract

An overlapping dinucleosome (OLDN) is a structure composed of one hexasome and one octasome and appears to be formed through nucleosome collision promoted by nucleosome remodeling factor(s). In this study, the solution structure of the OLDN was investigated through the integration of small-angle x-ray and neutron scattering (SAXS and SANS, respectively), computer modeling, and molecular dynamics simulations. Starting from the crystal structure, we generated a conformational ensemble based on normal mode analysis and searched for the conformations that reproduced the SAXS and SANS scattering curves well. We found that inclusion of histone tails, which are not observed in the crystal structure, greatly improved model quality. The obtained structural models suggest that OLDNs adopt a variety of conformations stabilized by histone tails situated at the interface between the hexasome and octasome, simultaneously binding to both the hexasomal and octasomal DNA. In addition, our models define a possible direction for the conformational changes or dynamics, which may provide important information that furthers our understanding of the role of chromatin dynamics in gene regulation.

Indexed as

HistonesNucleosomesChromatinScattering, Small AngleX-Ray DiffractionChromatinHistonesNucleosomes

Identifiers

PMID31952809
PMCPMC7202943
OpenAlexW2996546408

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.