Evidence map›Paper›PMID 25995270›Full record

ArticleGenome research2015

Topologically associating domains and their long-range contacts are established during early G1 coincident with the establishment of the replication-timing program.

Vishnu Dileep, Ferhat Ay, Jiao Sima, Daniel L Vera, William S Noble, David M Gilbert

Abstract read
In one paragraph

Article in Genome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing 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

95 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
  6. 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
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Genome folding dynamics during the M-to-G1-phase transition.Current opinion in genetics & development · 2023
    Review
  16. Review
  17. Article
  18. Maintaining Transcriptional Specificity Through Mitosis.Annual review of genomics and human genetics · 2022
    Review
  19. Article
  20. Review

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

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

6 authors.

Vishnu DileepDepartment of Biological Science, Florida State University, Tallahassee, Florida 32306, USA;
Ferhat AyDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;
Jiao SimaDepartment of Biological Science, Florida State University, Tallahassee, Florida 32306, USA;
Daniel L VeraCenter for Genomics and Personalized Medicine, Florida State University, Tallahassee, Florida 32306, USA.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;
David M GilbertDepartment of Biological Science, Florida State University, Tallahassee, Florida 32306, USA; Center for Genomics and Personalized Medicine, Florida State University, Tallahassee, Florida 32306, USA.

Funding

UNDERSTANDING MECHANISMS OF hESC SELF-RENEWAL AND CELL FATE COMMITMENTP01GM085354 · NIGMS · UNIVERSITY OF GEORGIA · PI DALTON, STEPHEN · 2008 to 2018
$18.3M
Genome Plasticity during ES Cell Differentiation to Neural LineagesR01GM083337 · NIGMS · SAN DIEGO BIOMEDICAL RESEARCH INSTITUTE · PI David M Gilbert · 2007 to 2026
$6.1M
The spatial organization of the Plasmodium genome throughout its infectious cycleR01AI106775 · NIAID · UNIVERSITY OF WASHINGTON · PI LE ROCH, KARINE GAELLE, NOBLE, WILLIAM STAFFORD · 2013 to 2016
$1.8M
MODIFIED SITE-SPECIFIC ENDONUCLEASE FOR GENOME RESEARCHR43HG000700 · NHGRI · PROMEGA CORPORATION · PI GOLUMBESKI, GEORGE S · 1992 to 1992
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NHGRI NIH HHS HG00700NIAID NIH HHS AI106775NIAID NIH HHS R01 AI106775NIGMS NIH HHS GM083337NIGMS NIH HHS GM085354NIGMS NIH HHS P01 GM085354NIGMS NIH HHS R01 GM083337
6 · The paper itself

Abstract

Mammalian genomes are partitioned into domains that replicate in a defined temporal order. These domains can replicate at similar times in all cell types (constitutive) or at cell type-specific times (developmental). Genome-wide chromatin conformation capture (Hi-C) has revealed sub-megabase topologically associating domains (TADs), which are the structural counterparts of replication domains. Hi-C also segregates inter-TAD contacts into defined 3D spatial compartments that align precisely to genome-wide replication timing profiles. Determinants of the replication-timing program are re-established during early G1 phase of each cell cycle and lost in G2 phase, but it is not known when TAD structure and inter-TAD contacts are re-established after their elimination during mitosis. Here, we use multiplexed 4C-seq to study dynamic changes in chromatin organization during early G1. We find that both establishment of TADs and their compartmentalization occur during early G1, within the same time frame as establishment of the replication-timing program. Once established, this 3D organization is preserved either after withdrawal into quiescence or for the remainder of interphase including G2 phase, implying 3D structure is not sufficient to maintain replication timing. Finally, we find that developmental domains are less well compartmentalized than constitutive domains and display chromatin properties that distinguish them from early and late constitutive domains. Overall, this study uncovers a strong connection between chromatin re-organization during G1, establishment of replication timing, and its developmental control.

Indexed as

DNA Replication TimingG1 PhaseAnimalsCell LineChromatinChromatin Assembly and DisassemblyEpithelial CellsGene Expression Regulation, DevelopmentalGenomeMiceSequence Analysis, DNAChromatin

Identifiers

PMID25995270
PMCPMC4509995

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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.