Evidence map›Paper›PMID 39191261›Full record

ArticleMolecular cell2024

RNA polymerases reshape chromatin architecture and couple transcription on individual fibers.

Thomas W Tullius, R Stefan Isaac, Danilo Dubocanin, Jane Ranchalis, L Stirling Churchman, Andrew B Stergachis

Abstract read
In one paragraph

Article in Molecular cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  7. Protamine lacunae preserve the paternal chromatin landscape in sperm.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. A haplotype-resolved view of human gene regulation.bioRxiv : the preprint server for biology · 2025
    Article
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  15. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Thomas W TulliusDepartment of Genetics, Harvard Medical School, Boston, MA 02115, USA.
R Stefan IsaacDepartment of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Danilo DubocaninDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
Jane RanchalisDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
L Stirling ChurchmanDepartment of Genetics, Harvard Medical School, Boston, MA 02115, USA. Electronic address: churchman@genetics.med.harvard.edu.
Andrew B StergachisDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA; Department of Genome Sciences, University of Washington, Seattle, WA, USA; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA. Electronic address: absterga@uw.edu.

Funding

Mechanisms of Transcriptional Control Revealed by Nascent Transcript SequencingR01HG007173 · NHGRI · HARVARD MEDICAL SCHOOL · PI Lee Stirling Churchman · 2013 to 2026
$6.7M
Investigating the contribution of non-coding genetic variation to rare disordersDP5OD029630 · OD · UNIVERSITY OF WASHINGTON · PI STERGACHIS, ANDREW BEN · 2020 to 2024
$1.9M
NHGRI NIH HHS R01 HG007173NIH HHS DP5 OD029630
6 · The paper itself

Abstract

RNA polymerases must initiate and pause within a complex chromatin environment, surrounded by nucleosomes and other transcriptional machinery. This environment creates a spatial arrangement along individual chromatin fibers ripe for both competition and coordination, yet these relationships remain largely unknown owing to the inherent limitations of traditional structural and sequencing methodologies. To address this, we employed long-read chromatin fiber sequencing (Fiber-seq) in Drosophila to visualize RNA polymerase (Pol) within its native chromatin context with single-molecule precision along up to 30 kb fibers. We demonstrate that Fiber-seq enables the identification of individual Pol II, nucleosome, and transcription factor footprints, revealing Pol II pausing-driven destabilization of downstream nucleosomes. Furthermore, we demonstrate pervasive direct distance-dependent transcriptional coupling between nearby Pol II genes, Pol III genes, and transcribed enhancers, modulated by local chromatin architecture. Overall, transcription initiation reshapes surrounding nucleosome architecture and couples nearby transcriptional machinery along individual chromatin fibers.

Indexed as

ChromatinDrosophila melanogasterNucleosomesTranscription, GeneticAnimalsChromatin Assembly and DisassemblyDNA-Directed RNA PolymerasesDrosophila ProteinsRNA Polymerase IIRNA Polymerase IIITranscription FactorsChromatinDNA-Directed RNA PolymerasesDrosophila ProteinsNucleosomesRNA Polymerase IIRNA Polymerase IIITranscription FactorschromatinFiber-seqnucleosomepromoter proximal pausingRNA Pol IIRNA Pol IIIsingle-moleculetranscription initiation

Identifiers

PMID39191261
PMCPMC11500009

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Registered trials

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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.