Evidence map›Paper›PMID 30507936›Full record

ArticlePLoS computational biology2018

Chain organization of human interphase chromosome determines the spatiotemporal dynamics of chromatin loci.

Lei Liu, Guang Shi, D Thirumalai, Changbong Hyeon

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Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

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  11. Transcription-induced active forces suppress chromatin motion.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
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  15. Polymer folding through active processes recreates features of genome organization.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  16. Article
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  19. Phase Separation and Correlated Motions in Motorized Genome.The journal of physical chemistry. B · 2022
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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.

Lei LiuKorea Institute for Advanced Study, Seoul, Korea.ORCID 0000-0001-8333-4775
Guang ShiBiophysics Program, Institute for Physical Science and Technology, University of Maryland, College Park, MD, USA.ORCID 0000-0002-4377-7210
D ThirumalaiDepartment of Chemistry, The University of Texas at Austin, Austin, TX, USA.
Changbong HyeonKorea Institute for Advanced Study, Seoul, Korea.ORCID 0000-0002-4844-7237

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigate spatiotemporal dynamics of human interphase chromosomes by employing a heteropolymer model that incorporates the information of human chromosomes inferred from Hi-C data. Despite considerable heterogeneities in the chromosome structures generated from our model, chromatins are organized into crumpled globules with space-filling (SF) statistics characterized by a single universal scaling exponent (ν = 1/3), and this exponent alone can offer a quantitative account of experimentally observed, many different features of chromosome dynamics. The local chromosome structures, whose scale corresponds to that of topologically associated domains (∼ 0.1 - 1 Mb), display dynamics with a fast relaxation time (≲ 1 - 10 sec); in contrast, the long-range spatial reorganization of the entire chromatin ([Formula: see text] Mb) occurs on a much slower time scale (≳ hour), providing the dynamic basis of cell-to-cell variability and glass-like behavior of chromosomes. Biological activities, modeled using stronger isotropic white noises added to active loci, accelerate the relaxation dynamics of chromatin domains associated with the low frequency modes and induce phase segregation between the active and inactive loci. Surprisingly, however, they do not significantly change the dynamics at local scales from those obtained under passive conditions. Our study underscores the role of chain organization of chromosome in determining the spatiotemporal dynamics of chromatin loci.

Indexed as

Models, GeneticAlgorithmsChromatinChromosomes, HumanChromosomes, Human, Pair 10Computational BiologyComputer SimulationEuchromatinHeterochromatinHumansInterphaseLymphocytesMolecular ConformationChromatinEuchromatinHeterochromatin

Identifiers

PMID30507936
PMCPMC6292649

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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.