Evidence map›Paper›PMID 23823730›Full record

ArticleNucleus (Austin, Tex.)

A polymer model explains the complexity of large-scale chromatin folding.

Mariano Barbieri, James Fraser, Liron-Mark Lavitas, Mita Chotalia, Josée Dostie, Ana Pombo, Mario Nicodemi

Abstract read
In one paragraph

Article in Nucleus (Austin, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. DNA-Topology Simplification by Topoisomerases.Molecules (Basel, Switzerland) · 2021
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Gene functioning and storage within a folded genome.Cellular & molecular biology letters · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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.

Mariano BarbieriUniversita' di Napoli "Federico II"; Dipartimento di Fisica; INFN Sezione di Napoli; CNR-SPIN, Complesso Universitario di Monte S. Angelo; Napoli, Italy; Department of Biochemistry and Goodman Cancer Research Center; McGill University; Montréal, Québec Canada; Berlin Institute for Medical Systems Biology; Max Delbrück Center for Molecular Medicine; Berlin-Buch, Germany; Genome Function Group; MRC Clinical Sciences Centre; Imperial College London; Hammersmith Hospital Campus; London, UK.
James Fraser
Liron-Mark Lavitas
Mita Chotalia
Josée Dostie
Ana Pombo
Mario Nicodemi

Funding

Medical Research Council MC_U120061476
6 · The paper itself

Abstract

The underlying global organization of chromatin within the cell nucleus has been the focus of intense recent research. Hi-C methods have allowed for the detection of genome-wide chromatin interactions, revealing a complex large-scale organization where chromosomes tend to partition into megabase-sized "topological domains" of local chromatin interactions and intra-chromosomal contacts extends over much longer scales, in a cell-type and chromosome specific manner. Until recently, the distinct chromatin folding properties observed experimentally have been difficult to explain in a single conceptual framework. We reported that a simple polymer-physics model of chromatin, the strings and binders switch (SBS) model, succeeds in describing the full range of chromatin configurations observed in vivo. The SBS model simulates the interactions between randomly diffusing binding molecules and binding sites on a polymer chain. It explains how polymer architectural patterns can be established, how different stable conformations can be produced and how conformational changes can be reliably regulated by simple strategies, such as protein upregulation or epigenetic modifications, via fundamental thermodynamics mechanisms.

Indexed as

Cell NucleusChromatinHumansModels, MolecularPolymersChromatinPolymerschromatin organizationFISHHi-Cpolymer physicsstatistical mechanics

Identifiers

PMID23823730
PMCPMC3810333

What OpenQuestion holds

Textmetadata
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.