Evidence map›Paper›PMID 40923758›Full record

ArticleNucleic acids research2025

Native nucleosome-positioning elements as alternatives to the 601 sequence for nucleosome repositioning studies.

Ruo-Wen Chen, Shane D Stoeber, Ilana M Nodelman, Hengye Chen, Wenxuan Yang, Gregory D Bowman, Lu Bai, Michael G Poirier

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Cohesin Facilitates Nucleosome Invasion by Transcription Factors.bioRxiv : the preprint server for biology · 2025
    Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Ruo-Wen ChenOhio State Biochemistry Graduate Program, The Ohio State University, Columbus, OH 43210, United States.
Shane D StoeberDepartment of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, The Pennsylvania State University, University Park, PA 16802, United States.
Ilana M NodelmanTC Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, United States.
Hengye ChenDepartment of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, The Pennsylvania State University, University Park, PA 16802, United States.
Wenxuan YangDepartment of Physics, The Ohio State University, Columbus, OH 43210, United States.
Gregory D BowmanTC Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, United States.ORCID 0000-0001-8025-4315
Lu BaiDepartment of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, The Pennsylvania State University, University Park, PA 16802, United States.
Michael G PoirierOhio State Biochemistry Graduate Program, The Ohio State University, Columbus, OH 43210, United States.ORCID 0000-0002-1563-5792

Funding

Structural and Functional Characterization of the Chd1 Chromatin RemodelerR01GM084192 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BOWMAN, GREGORY DEAN · 2008 to 2024
$6.3M
Mechanism of Chromatin Accessibility, 3D Chromosome Organization, and Their Functions in Gene RegulationR35GM139654 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Lu Bai · 2021 to 2026
$3.8M
Mechanisms of chromatin regulation of transcriptionR35GM139564 · NIGMS · OHIO STATE UNIVERSITY · PI POIRIER, MICHAEL GUY · 2021 to 2025
$3.6M
Typhoon FLA9500 Biomedical ImagerS10OD023582 · OD · OHIO STATE UNIVERSITY · PI JACKMAN, JANE ELIZABETH · 2017 to 2017
$144k
National Science Foundation MCB 2411725NIGMS NIH HHS R01 GM084192NIGMS NIH HHS R35 GM139564NIGMS NIH HHS R35 GM139654NIH HHS R01 GM084192NIH HHS R35 GM139564NIH HHS R35 GM139654NIH HHS S10 OD023582NIH HHS S10OD023582
6 · The paper itself

Abstract

Nucleosome repositioning is essential for establishing nucleosome-depleted regions to initiate transcription. This process has been extensively studied using structural, biochemical, and single-molecule approaches, which require homogeneously positioned nucleosomes. This is often achieved using the Widom 601 sequence, a highly efficient nucleosome-positioning element (NPE) selected for its unusually strong binding to the H3-H4 histone tetramer. Due to the artificial nature of 601, native NPEs are needed to explore the role of DNA sequence in nucleosome repositioning. Here, we characterize the position distributions and nucleosome formation free energies for a set of yeast native nucleosomes from Saccharomyces cerevisiae. We show these native NPEs can be used in biochemical studies of nucleosome repositioning by transcription factors (TFs) and the chromatin remodeler Chd1. TFs could directly reposition a fraction of nucleosomes containing native NPEs, but not 601-containing nucleosomes. In contrast, partial unwrapping was similar for 601 and native NPE sequences, and the rate of ATP-dependent remodeling by Chd1 was within the range of the fast and slow directions of the 601 nucleosomes. This set of native NPEs provides an alternative to the 601 NPE that can be used for probing the repositioning of nucleosomes that contain native DNA sequences.

Indexed as

NucleosomesBase SequenceChromatin Assembly and DisassemblyDNA-Binding ProteinsHistonesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription FactorsCHD1 protein, S cerevisiaeDNA-Binding ProteinsHistonesNucleosomesSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID40923758
PMCPMC12412783

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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.