Evidence map›Paper›PMID 39549698›Full record

ArticleCell2025

The single-molecule accessibility landscape of newly replicated mammalian chromatin.

Megan S Ostrowski, Marty G Yang, Colin P McNally, Nour J Abdulhay, Simai Wang, Keerthi Renduchintala, Iryna Irkliyenko, Alva Biran, Brandon T L Chew, Ayush D Midha and 7 more

Abstract read
In one paragraph

Article in Cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  18. Acute multi-level response to defectivebioRxiv : the preprint server for biology · 2024
    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

17 authors.

Megan S OstrowskiGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA.
Marty G YangGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA.
Colin P McNallyGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA; UCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA.
Nour J AbdulhayGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA; UCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA.
Simai WangGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA.
Keerthi RenduchintalaGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA.
Iryna IrkliyenkoGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA.
Alva BiranNovo Nordisk Foundation Center for Protein Research, University of Copenhagen, 2200 Copenhagen, Denmark.
Brandon T L ChewGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.
Ayush D MidhaGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.
Emily V WongUCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA.
Jonathan SandovalDepartment of Cellular and Molecular Pharmacology, UCSF, San Francisco, CA 94158, USA.
Isha H JainGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.
Anja GrothNovo Nordisk Foundation Center for Protein Research, University of Copenhagen, 2200 Copenhagen, Denmark; Department of Cellular and Molecular Medicine (ICMM), University of Copenhagen, 2200 Copenhagen, Denmark.
Elphège P NoraUCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA; Cardiovascular Research Institute, UCSF, San Francisco, CA 94158, USA; Chan-Zuckerberg BioHub, San Francisco, CA 94158, USA.
Hani GoodarziUCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA; Chan-Zuckerberg BioHub, San Francisco, CA 94158, USA; Helen Diller Cancer Research Center, UCSF, San Francisco, CA 94158, USA; Bakar Computational Health Sciences Institute, UCSF, San Francisco, CA 94158, USA.
Vijay RamaniGladstone Institute for Data Science & Biotechnology, San Francisco, CA 94158, USA; UCSF Department of Biochemistry & Biophysics, San Francisco, CA 94158, USA; Helen Diller Cancer Research Center, UCSF, San Francisco, CA 94158, USA; Bakar Computational Health Sciences Institute, UCSF, San Francisco, CA 94158, USA. Electronic address: vijay.ramani@gladstone.ucsf.edu.

Funding

NRSA Hepatology Training GrantT32DK060414 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Mandana Khalili, JACQUELYN J. MAHER · 2002 to 2026
$6.8M
SINGLE-CELL CHEMICAL TRANSCRIPTOMIC DISSECTION OF AN ESSENTIAL TRANSCRIPTION FACTOR NETWORKDP2HG012442 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RAMANI, VIJAY · 2021 to 2024
$2.6M
Investigating the role of genome folding in transcriptional regulationR35GM142792 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI NORA, ELPHEGE-PIERRE JULIEN · 2021 to 2025
$2.0M
NHGRI NIH HHS DP2 HG012442NIDDK NIH HHS T32 DK060414NIGMS NIH HHS R35 GM142792
6 · The paper itself

Abstract

We present replication-aware single-molecule accessibility mapping (RASAM), a method to nondestructively measure replication status and protein-DNA interactions on chromatin genome-wide. Using RASAM, we uncover a genome-wide state of single-molecule "hyperaccessibility" post-replication that resolves over several hours. Combining RASAM with cellular models for rapid protein degradation, we demonstrate that histone chaperone CAF-1 reduces nascent chromatin accessibility by filling single-molecular "gaps" and generating closely spaced dinucleosomes on replicated DNA. At cis-regulatory elements, we observe unique modes by which nascent chromatin hyperaccessibility resolves: at CCCTC-binding factor (CTCF)-binding sites, CTCF and nucleosomes compete, reducing CTCF occupancy and motif accessibility post-replication; at active transcription start sites, high chromatin accessibility is maintained, implying rapid re-establishment of nucleosome-free regions. Our study introduces a new paradigm for studying replicated chromatin fiber organization. More broadly, we uncover a unique organization of newly replicated chromatin that must be reset by active processes, providing a substrate for epigenetic reprogramming.

Indexed as

ChromatinDNA ReplicationSingle Molecule ImagingAnimalsBinding SitesCCCTC-Binding FactorHumansMiceNucleosomesCCCTC-Binding FactorChromatinNucleosomeschromatinDNA replicationepigeneticsepigenomicsgenome architecturemolecular methodsnucleosomestranscriptiontranscription factors

Identifiers

PMID39549698
PMCPMC12176082

What OpenQuestion holds

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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.