Evidence map›Paper›PMID 38137015›Full record

ArticleGenes2023

Polymer Modeling Reveals Interplay between Physical Properties of Chromosomal DNA and the Size and Distribution of Condensin-Based Chromatin Loops.

Daniel Kolbin, Benjamin L Walker, Caitlin Hult, John Donoghue Stanton, David Adalsteinsson, M Gregory Forest, Kerry Bloom

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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

7 authors at 3 institutions in 1 country.

Daniel KolbinDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Benjamin L WalkerDepartment of Mathematics, University of California-Irvine, Irvine, CA 92697, USA.
Caitlin HultDepartment of Mathematics, Gettysburg College, Gettysburg, PA 17325, USA.ORCID 0000-0002-2641-2180
John Donoghue StantonDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
David AdalsteinssonDepartment of Mathematics and Carolina Center for Interdisciplinary Applied Mathematics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
M Gregory ForestDepartment of Mathematics and Carolina Center for Interdisciplinary Applied Mathematics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.ORCID 0000-0002-7718-4456
Kerry BloomDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.ORCID 0000-0002-3457-004X
University of North Carolina at Chapel Hill · USGettysburg College · USUniversity of California, Irvine · US

Funding

Structure and Function of a Eukaryotic CentromereR01GM032238 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S · 1985 to 2025
$6.2M
NIGMS NIH HHS R01 GM032238
6 · The paper itself

Abstract

Transient DNA loops occur throughout the genome due to thermal fluctuations of DNA and the function of SMC complex proteins such as condensin and cohesin. Transient crosslinking within and between chromosomes and loop extrusion by SMCs have profound effects on high-order chromatin organization and exhibit specificity in cell type, cell cycle stage, and cellular environment. SMC complexes anchor one end to DNA with the other extending some distance and retracting to form a loop. How cells regulate loop sizes and how loops distribute along chromatin are emerging questions. To understand loop size regulation, we employed bead-spring polymer chain models of chromatin and the activity of an SMC complex on chromatin. Our study shows that (1) the stiffness of the chromatin polymer chain, (2) the tensile stiffness of chromatin crosslinking complexes such as condensin, and (3) the strength of the internal or external tethering of chromatin chains cooperatively dictate the loop size distribution and compaction volume of induced chromatin domains. When strong DNA tethers are invoked, loop size distributions are tuned by condensin stiffness. When DNA tethers are released, loop size distributions are tuned by chromatin stiffness. In this three-way interaction, the presence and strength of tethering unexpectedly dictates chromatin conformation within a topological domain.

Indexed as

Chromosomal Proteins, Non-HistonePolymersAdenosine TriphosphatasesCell Cycle ProteinsChromatinDNADNA-Binding ProteinsMultiprotein ComplexesAdenosine TriphosphatasesCell Cycle ProteinsChromatinChromosomal Proteins, Non-Histonecondensin complexesDNADNA-Binding ProteinsMultiprotein ComplexesPolymerschromatin organizationcrosslinkersDNA loopsloop regulationnuclear tetherspolymer modelingSMC complexes

Identifiers

PMID38137015
PMCPMC10742461
OpenAlexW4389560253

What OpenQuestion 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 OpenQuestion graph.