Evidence map›Paper›PMID 24990374›Full record

ArticleNucleic acids research2014

Spatial confinement is a major determinant of the folding landscape of human chromosomes.

Gamze Gürsoy, Yun Xu, Amy L Kenter, Jie Liang

Abstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
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  4. Energy landscape analysis of the development of the chromosome structure across the cell cycle.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
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  7. Modeling properties of chromosome territories using polymer filaments in diverse confinement geometries.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2024
    Article
  8. Review
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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.

Gamze GürsoyDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.
Yun XuDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.
Amy L KenterDepartment of Microbiology and Immunology, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Jie LiangDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA jliang@uic.edu.

Funding

Chicago Tri-Institutional Center for Chemical Methods and Library DevelopmentP50GM086145 · NIGMS · UNIVERSITY OF CHICAGO · PI KOZMIN, SERGEY A · 2008 to 2012
$9.9M
Factors and DNA Motifs Involved in Ig Class SwitchR01AI052400 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KENTER, AMY L · 2003 to 2012
$3.7M
Computational assembly of beta-barrel membrane proteinsR01GM079804 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LIANG, JIE · 2007 to 2016
$2.8M
Class switch recombination during early B cell developmentR21AI106328 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KENTER, AMY L · 2013 to 2014
$424k
NIAID NIH HHS R01AI052400NIAID NIH HHS R21AI106328NIGMS NIH HHS GM079804NIGMS NIH HHS GM086145NIGMS NIH HHS R01 GM079804
6 · The paper itself

Abstract

The global architecture of the cell nucleus and the spatial organization of chromatin play important roles in gene expression and nuclear function. Single-cell imaging and chromosome conformation capture-based techniques provide a wealth of information on the spatial organization of chromosomes. However, a mechanistic model that can account for all observed scaling behaviors governing long-range chromatin interactions is missing. Here we describe a model called constrained self-avoiding chromatin (C-SAC) for studying spatial structures of chromosomes, as the available space is a key determinant of chromosome folding. We studied large ensembles of model chromatin chains with appropriate fiber diameter, persistence length and excluded volume under spatial confinement. We show that the equilibrium ensemble of randomly folded chromosomes in the confined nuclear volume gives rise to the experimentally observed higher-order architecture of human chromosomes, including average scaling properties of mean-square spatial distance, end-to-end distance, contact probability and their chromosome-to-chromosome variabilities. Our results indicate that the overall structure of a human chromosome is dictated by the spatial confinement of the nuclear space, which may undergo significant tissue- and developmental stage-specific size changes.

Indexed as

AlgorithmsCell Nucleus SizeChromatinChromosomes, HumanHumansModels, MolecularNucleic Acid ConformationChromatin

Identifiers

PMID24990374
PMCPMC4117743

What OpenQuestion holds

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LicenceCC BY
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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.