Evidence map›Paper›PMID 30962387›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Synergy of topoisomerase and structural-maintenance-of-chromosomes proteins creates a universal pathway to simplify genome topology.

Enzo Orlandini, Davide Marenduzzo, Davide Michieletto

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Article
  7. Mitotic genome folding.The Journal of cell biology · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Dynamics of chromosome organization in a minimal bacterial cell.Frontiers in cell and developmental biology · 2023
    Article
  15. Article
  16. Topological gelation of reconnecting polymers.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Review
  19. Article
  20. 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

3 authors.

Enzo OrlandiniDipartimento di Fisica e Astronomia "Galileo Galilei," Sezione Istituto Nazionale di Fisica Nucleare, Università degli Studi di Padova, I-35131 Padova, Italy.
Davide MarenduzzoSchool of Physics and Astronomy, University of Edinburgh, Edinburgh EH9 3FD, United Kingdom.
Davide MichielettoSchool of Physics and Astronomy, University of Edinburgh, Edinburgh EH9 3FD, United Kingdom davide.michieletto@ed.ac.uk.ORCID 0000-0003-2186-6869

Funding

European Research Council
6 · The paper itself

Abstract

Topological entanglements severely interfere with important biological processes. For this reason, genomes must be kept unknotted and unlinked during most of a cell cycle. Type II topoisomerase (TopoII) enzymes play an important role in this process but the precise mechanisms yielding systematic disentanglement of DNA in vivo are not clear. Here we report computational evidence that structural-maintenance-of-chromosomes (SMC) proteins-such as cohesins and condensins-can cooperate with TopoII to establish a synergistic mechanism to resolve topological entanglements. SMC-driven loop extrusion (or diffusion) induces the spatial localization of essential crossings, in turn catalyzing the simplification of knots and links by TopoII enzymes even in crowded and confined conditions. The mechanism we uncover is universal in that it does not qualitatively depend on the specific substrate, whether DNA or chromatin, or on SMC processivity; we thus argue that this synergy may be at work across organisms and throughout the cell cycle.

Indexed as

GenomeAdenosine TriphosphatasesCell CycleCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsDNADNA-Binding ProteinsDNA Topoisomerases, Type IIMultiprotein ComplexesAdenosine TriphosphatasesCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinscondensin complexesDNADNA-Binding ProteinsDNA Topoisomerases, Type IIMultiprotein ComplexesBrownian dynamicsentanglementsgenome topologySMC proteinstopoisomerase

Identifiers

PMID30962387
PMCPMC6486742

What OpenQuestion holds

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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.