Evidence map›Paper›PMID 37891161›Full record

ArticleNature communications2023

Chromatinization modulates topoisomerase II processivity.

Jaeyoon Lee, Meiling Wu, James T Inman, Gundeep Singh, Seong Ha Park, Joyce H Lee, Robert M Fulbright, Yifeng Hong, Joshua Jeong, James M Berger and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Mitotic genome folding.The Journal of cell biology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Jaeyoon LeePhysics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.
Meiling WuPhysics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0001-8827-2999
James T InmanPhysics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.
Gundeep SinghBiophysics Program, Cornell University, Ithaca, NY, 14853, USA.
Seong Ha ParkBiophysics Program, Cornell University, Ithaca, NY, 14853, USA.
Joyce H LeeDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.ORCID 0000-0003-0459-5999
Robert M FulbrightPhysics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.
Yifeng HongDepartment of Electrical and Computer Engineering, Cornell University, Ithaca, NY, 14853, USA.
Joshua JeongDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
James M BergerDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.ORCID 0000-0003-0666-1240
Michelle D WangPhysics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA. mwang@physics.cornell.edu.ORCID 0000-0001-9137-3790

Funding

TRAINING IN MOLECULAR PHYSICS OF BIOLOGICAL SYSTEMST32GM008267 · NIGMS · CORNELL UNIVERSITY ITHACA · PI WANG, MICHELLE D. · 1988 to 2021
$9.6M
Structural and Biochemical Analyses of Type II DNA TopoisomerasesR01CA077373 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BERGER, JAMES M. · 1999 to 2021
$7.6M
Understanding and exploiting DNA topoisomerases in cancer biologyR35CA263778 · NCI · JOHNS HOPKINS UNIVERSITY · PI James M. Berger · 2021 to 2026
$5.0M
Fundamental Biological Processes Under TorsionR01GM136894 · NIGMS · CORNELL UNIVERSITY · PI WANG, MICHELLE D. · 2020 to 2023
$1.2M
NCI NIH HHS R01 CA077373NCI NIH HHS R35 CA263778NIGMS NIH HHS R01 GM136894NIGMS NIH HHS T32 GM008267
6 · The paper itself

Abstract

Type IIA topoisomerases are essential DNA processing enzymes that must robustly and reliably relax DNA torsional stress. While cellular processes constantly create varying torsional stress, how this variation impacts type IIA topoisomerase function remains obscure. Using multiple single-molecule approaches, we examined the torsional dependence of eukaryotic topoisomerase II (topo II) activity on naked DNA and chromatin. We observed that topo II is ~50-fold more processive on buckled DNA than previously estimated. We further discovered that topo II relaxes supercoiled DNA prior to plectoneme formation, but with processivity reduced by ~100-fold. This relaxation decreases with diminishing torsion, consistent with topo II capturing transient DNA loops. Topo II retains high processivity on buckled chromatin (~10,000 turns) and becomes highly processive even on chromatin under low torsional stress (~1000 turns), consistent with chromatin's predisposition to readily form DNA crossings. This work establishes that chromatin is a major stimulant of topo II function.

Indexed as

DNADNA Topoisomerases, Type IIChromatinDNA Topoisomerases, Type IEukaryotic CellsChromatinDNADNA Topoisomerases, Type IDNA Topoisomerases, Type II

Identifiers

PMID37891161
PMCPMC10611788

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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.