Evidence map›Paper›PMID 34192585›Full record

ArticleJournal of molecular biology2021

Surprising Twists in Nucleosomal DNA with Implication for Higher-order Folding.

Stefjord Todolli, Robert T Young, Abigail S Watkins, Antonio Bu Sha, John Yager, Wilma K Olson

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. Article
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  7. Article
  8. Twisting DNA by salt.Nucleic acids research · 2022
    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

6 authors at 1 institution in 1 country.

Stefjord TodolliDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
Robert T YoungDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
Abigail S WatkinsDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
Antonio Bu ShaDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
John YagerDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
Wilma K OlsonDepartment of Chemistry & Chemical Biology, Center for Quantitative Biology, Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA. Electronic address: wilma.olson@rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

THEORETICFAL ASPECTS OF DNA SUPERCOILINGR01GM034809 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI OLSON, WILMA K · 1985 to 2019
$4.6M
NIGMS NIH HHS R01 GM034809
6 · The paper itself

Abstract

While nucleosomes are dynamic entities that must undergo structural deformations to perform their functions, the general view from available high-resolution structures is a largely static one. Even though numerous examples of twist defects have been documented, the DNA wrapped around the histone core is generally thought to be overtwisted. Analysis of available high-resolution structures from the Protein Data Bank reveals a heterogeneous distribution of twist along the nucleosomal DNA, with clear patterns that are consistent with the literature, and a significant fraction of structures that are undertwisted. The subtle differences in nucleosomal DNA folding, which extend beyond twist, have implications for nucleosome disassembly and modeled higher-order structures. Simulations of oligonucleosome arrays built with undertwisted models behave very differently from those constructed from overtwisted models, in terms of compaction and inter-nucleosome contacts, introducing configurational changes equivalent to those associated with 2-3 base-pair changes in nucleosome spacing. Differences in the nucleosomal DNA pathway, which underlie the way that DNA enters and exits the nucleosome, give rise to different nucleosome-decorated minicircles and affect the topological mix of configurational states.

Indexed as

Chromatin Assembly and DisassemblyNucleic Acid ConformationDNAHistonesModels, MolecularNucleosomesDNAHistonesNucleosomesDNA minicircleMonte Carlo DNA simulationnucleosomal twist uptakenucleosome gapingoligonucleosome arrayundertwisted nucleosome

Identifiers

PMID34192585
PMCPMC8380738
OpenAlexW3175258316

What OpenQuestion holds

Textmetadata
LicenceTDM
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.