Evidence map›Paper›PMID 28991264›Full record

ArticleNature structural & molecular biology2017

Architectural alterations of the fission yeast genome during the cell cycle.

Hideki Tanizawa, Kyoung-Dong Kim, Osamu Iwasaki, Ken-Ichi Noma

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
  2. Article
  3. A Translocation within thebioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Organization principles of dynamic three-dimensional genome architecture associated with centromere clustering states.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  14. Histone deacetylation and cytosine methylation compartmentalize heterochromatic regions in the genome organization ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
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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

4 authors.

Hideki TanizawaThe Wistar Institute, Philadelphia, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-2573-2473
Kyoung-Dong KimThe Wistar Institute, Philadelphia, Pennsylvania, USA.
Osamu IwasakiThe Wistar Institute, Philadelphia, Pennsylvania, USA.
Ken-Ichi NomaThe Wistar Institute, Philadelphia, Pennsylvania, USA.ORCID http://orcid.org/0000-0002-5187-6788

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$75.9M
A New Methodology to Decipher Three-Dimensional Genome StructureDP2OD004348 · OD · WISTAR INSTITUTE · PI NOMA, KENICHI · 2008 to 2008
$3.1M
Condensin connects 3D genome organization, chromosomal segregation, andgene regulation via its interactions with transcription-related factors.R01GM124195 · NIGMS · WISTAR INSTITUTE · PI NOMA, KENICHI · 2017 to 2020
$1.8M
NCI NIH HHS P30 CA010815NIGMS NIH HHS R01 GM124195NIH HHS DP2 OD004348
6 · The paper itself

Abstract

Eukaryotic genomes are highly ordered through various mechanisms, including topologically associating domain (TAD) organization. We employed an in situ Hi-C approach to follow the 3D organization of the fission yeast genome during the cell cycle. We demonstrate that during mitosis, large domains of 300 kb-1 Mb are formed by condensin. This mitotic domain organization does not suddenly dissolve, but gradually diminishes until the next mitosis. By contrast, small domains of 30-40 kb that are formed by cohesin are relatively stable across the cell cycle. Condensin and cohesin mediate long- and short-range contacts, respectively, by bridging their binding sites, thereby forming the large and small domains. These domains are inversely regulated during the cell cycle but assemble independently. Our study describes the chromosomal oscillation between the formation and decay phases of the large and small domains, and we predict that the condensin-mediated domains serve as chromosomal compaction units.

Indexed as

Genome, FungalMitosisAdenosine TriphosphatasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosomes, FungalCohesinsDNA-Binding ProteinsFungal ProteinsMultiprotein ComplexesSchizosaccharomycesAdenosine TriphosphatasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinscondensin complexesDNA-Binding ProteinsFungal ProteinsMultiprotein Complexes

Identifiers

PMID28991264
PMCPMC5724045

What OpenQuestion holds

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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.