Evidence map›Paper›PMID 39110499›Full record

ArticleeLife2024

Chromosome structure in

Xinyang Bing, Wenfan Ke, Miki Fujioka, Amina Kurbidaeva, Sarah Levitt, Mike Levine, Paul Schedl, James B Jaynes

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Reversing aging-like 3D genome disorganization in abioRxiv : the preprint server for biology · 2026
    Article
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  14. ThebioRxiv : the preprint server for biology · 2025
    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

8 authors.

Xinyang Bing *Lewis Sigler Institute, Princeton University, Princeton, United States.ORCID https://orcid.org/0000-0001-6789-1918
Wenfan Ke *Department of Molecular Biology, Princeton University, Princeton, United States.ORCID https://orcid.org/0000-0002-7047-5445
Miki Fujioka *Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, United States.
Amina KurbidaevaDepartment of Molecular Biology, Princeton University, Princeton, United States.
Sarah LevittDepartment of Molecular Biology, Princeton University, Princeton, United States.
Mike LevineLewis Sigler Institute, Princeton University, Princeton, United States.
Paul SchedlDepartment of Molecular Biology, Princeton University, Princeton, United States.ORCID https://orcid.org/0000-0001-5704-2349
James B JaynesDepartment of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, United States.ORCID https://orcid.org/0000-0001-7943-794X

Funding

Visualization of gene activity in the Drosophila embryoR35GM118147 · NIGMS · PRINCETON UNIVERSITY · PI Michael Steven Levine · 2016 to 2026
$6.7M
Control of the 4D chromatin landscape underlying gene activity during developmentU01DK127429 · NIDDK · PRINCETON UNIVERSITY · PI GREGOR, THOMAS, LEVINE, MICHAEL STEVEN · 2020 to 2024
$3.2M
Genetic regulatory mechanism in development and differentiationR35GM126975 · NIGMS · PRINCETON UNIVERSITY · PI SCHEDL, PAUL D · 2018 to 2022
$3.0M
Non-canonical functions of chromatin insulators and Polycomb-group proteinsR01GM137062 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI JAYNES, JAMES B · 2020 to 2023
$1.2M
Histochemical Society Keystone GrantNew Jersey Commission on Cancer Research COCR23PDF011NIDDK NIH HHS U01 DK127429NIGMS NIH HHS R01 GM137062NIGMS NIH HHS R35 GM118147NIGMS NIH HHS R35 GM126975
6 · The paper itself

Abstract

Two different models have been proposed to explain how the endpoints of chromatin looped domains ('TADs') in eukaryotic chromosomes are determined. In the first, a cohesin complex extrudes a loop until it encounters a boundary element roadblock, generating a stem-loop. In this model, boundaries are functionally autonomous: they have an intrinsic ability to halt the movement of incoming cohesin complexes that is independent of the properties of neighboring boundaries. In the second, loops are generated by boundary:boundary pairing. In this model, boundaries are functionally non-autonomous, and their ability to form a loop depends upon how well they match with their neighbors. Moreover, unlike the loop-extrusion model, pairing interactions can generate both stem-loops and circle-loops. We have used a combination of MicroC to analyze how TADs are organized, and experimental manipulations of the

Indexed as

DrosophilaAnimalsCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneChromosome StructuresCohesinsDrosophila melanogasterDrosophila ProteinsCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsDrosophila Proteinsboundary:boundary pairingboundary elementschromatin insulatorschromosomescohesin loop extrusionD. melanogastergene activationgene expressionloop topologyTADs

Identifiers

PMID39110499
PMCPMC11305675

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.