Evidence map›Paper›PMID 29225036›Full record

ArticleMolecular cell2017

Transcription and Remodeling Produce Asymmetrically Unwrapped Nucleosomal Intermediates.

Srinivas Ramachandran, Kami Ahmad, Steven Henikoff

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

96 citing papers in PubMed, 147 citations in OpenAlex.

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  7. Cell-Free DNA-Based Methods to Map Chromatin.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Rotational settings quantize nucleosome movement by chromatin regulators.bioRxiv : the preprint server for biology · 2025
    Article
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36 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Srinivas RamachandranBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Howard Hughes Medical Institute, Seattle, WA 98109, USA.
Kami AhmadBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Steven HenikoffBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Howard Hughes Medical Institute, Seattle, WA 98109, USA. Electronic address: steveh@fhcrc.org.
Fred Hutch Cancer Center · USHoward Hughes Medical Institute · US

Funding

Development and architecture of epigenetic regulatory elementsR01GM108699 · NIGMS · HARVARD MEDICAL SCHOOL · PI AHMAD, KAMRAN · 2014 to 2017
$1.3M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM108699
6 · The paper itself

Abstract

Nucleosomes are disrupted during transcription and other active processes, but the structural intermediates during nucleosome disruption in vivo are unknown. To identify intermediates, we mapped subnucleosomal protections in Drosophila cells using Micrococcal Nuclease followed by sequencing. At the first nucleosome position downstream of the transcription start site, we identified unwrapped intermediates, including hexasomes that lack either proximal or distal contacts. Inhibiting topoisomerases or depleting histone chaperones increased unwrapping, whereas inhibiting release of paused RNAPII or reducing RNAPII elongation decreased unwrapping. Our results indicate that positive torsion generated by elongating RNAPII causes transient loss of histone-DNA contacts. Using this mapping approach, we found that nucleosomes flanking human CTCF insulation sites are similarly disrupted. We also identified diagnostic subnucleosomal particle remnants in cell-free human DNA data as a relic of transcribed genes from apoptosing cells. Thus identification of subnucleosomal fragments from nuclease protection data represents a general strategy for structural epigenomics.

Indexed as

Chromatin Assembly and DisassemblyEpigenomicsGene Expression RegulationTranscription, GeneticAnimalsCarrier ProteinsCells, CulturedDrosophila melanogasterDrosophila ProteinsHistonesMicrococcal NucleaseNucleosomesRNA Polymerase IITranscription Initiation SiteCarrier ProteinsDrosophila ProteinsFACT protein, DrosophilaHistonesMicrococcal NucleaseNucleosomesRNA Polymerase IIcell-free DNAhexasomestructural epigenomicssubnucleosometorsional straintranscription elongation

Identifiers

PMID29225036
PMCPMC6421108
OpenAlexW2774305370

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.