Evidence map›Paper›PMID 41028835›Full record

ArticleNature cell biology2025

Phase-separated NDF-FACT condensates facilitate transcription elongation on chromatin.

Ziwei Li, Francesca Burgos-Bravo, Kevin Xu, Chen Li, Kelvin Y Kwan, Alexander B Tong, Zelin Shan, Huan Wang, Motoki Takaku, Joey Li and 4 more

Abstract read
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Current Challenges of Transcription Compartmentalization Research.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  3. Article
  4. 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

14 authors.

Ziwei Li *Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Francesca Burgos-Bravo *Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA.
Kevin XuDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Chen LiCalifornia Institute for Quantitative Biosciences, University of California, Berkeley, CA, USA.
Kelvin Y KwanDepartment of Cell Biology and Neurosciences, Rutgers University, Piscataway, NJ, USA.
Alexander B TongCalifornia Institute for Quantitative Biosciences, University of California, Berkeley, CA, USA.ORCID http://orcid.org/0000-0003-3793-2533
Zelin ShanThe Salk Institute for Biological Studies, La Jolla, CA, USA.
Huan WangDepartment of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, USA.ORCID http://orcid.org/0000-0001-7549-5026
Motoki TakakuDepartment of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, USA.
Joey LiDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Zheng ShiDepartment of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, USA.ORCID http://orcid.org/0000-0002-5214-1871
Dmitry LyumkisThe Salk Institute for Biological Studies, La Jolla, CA, USA.
Carlos BustamanteDepartment of Molecular and Cell Biology, University of California, Berkeley, CA, USA. carlosb@berkeley.edu.ORCID http://orcid.org/0000-0002-2970-0073
Jia FeiDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA. jia.fei@rutgers.edu.ORCID http://orcid.org/0000-0003-0612-6176

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Structural Biology CoreU54AI170855 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI Karen A Kirby · 2022 to 2026
$36.7M
THE PHYSICAL CHEMISTRY OF NUCLEIC ACIDSR01GM032543 · NIGMS · UNIVERSITY OF OREGON · PI CARLOS Jose BUSTAMANTE · 1985 to 2026
$6.4M
Structural basis for activity of and resistance to HIV integrase inhibitorsU01AI136680 · NIAID · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LYUMKIS, DMITRY · 2022 to 2025
$3.4M
PHYSICAL CHEMISTRY OF NUCLEIC ACIDSR37GM032543 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BUSTAMANTE, CARLOS JOSE · 1999 to 2008
$2.4M
Chromatin modifications that enhance DNA accessibilityR01GM151305 · NIGMS · NORTHEASTERN UNIVERSITY · PI MARK C WILLIAMS · 2023 to 2026
$2.0M
Understanding the viscoelasticity, surface tension, and membrane interactions of biomolecular condensates in live cellsR35GM147027 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI Zheng Shi · 2022 to 2026
$1.6M
Role of nucleosome architecture in cellular reprogrammingR01GM148729 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI Motoki Takaku · 2023 to 2026
$1.4M
Investigate the function of NDF in chromatin dynamics and gene expressionR01GM145748 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI Jia Fei · 2023 to 2026
$1.3M
Howard Hughes Medical Institute (HHMI) InvestigatorNational Science Foundation (NSF) MCB-2048095NCI NIH HHS P30 CA014195NIAID NIH HHS U01 AI136680NIAID NIH HHS U54 AI170855NIGMS NIH HHS R01 GM032543NIGMS NIH HHS R01 GM145748NIGMS NIH HHS R01 GM148729NIGMS NIH HHS R01 GM151305NIGMS NIH HHS R35 GM147027NIGMS NIH HHS R37 GM032543U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA014195U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) U54AI170855U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM032543U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM145748U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM148729U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM151305U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM147027
6 · The paper itself

Abstract

How the facilitates chromatin transcription (FACT) complex enables RNA polymerase II to overcome chromatin barriers in cells remains poorly understood-especially given the limited direct interactions of FACT with polymerases, DNA or nucleosomes. Here we demonstrate that phase separation, mediated by nucleosome destabilizing factor (NDF), is a key mechanism enabling the function of FACT during transcription elongation. Through biochemical and single-molecule assays, we found that NDF-FACT condensates create specialized biochemical environments that enhance transcription efficiency approximately 20-fold compared with FACT alone. These dynamic condensates form on transcribing RNA polymerase II and travel along chromatin, where they promote efficient nucleosome disassembly at barriers while retaining histones on DNA to preserve chromatin integrity. In human stem cells, disruption of these condensates leads to genome-wide transcriptional defects and chromatin instability, mirroring the effects of FACT depletion. By showing that phase separation enhances FACT function during transcription elongation, our study reveals a key mechanism that preserves chromatin integrity and transcriptional homeostasis in human stem cells.

Indexed as

ChromatinDNA-Binding ProteinsHigh Mobility Group ProteinsTranscriptional Elongation FactorsTranscription Elongation, GeneticTranscription, GeneticChromatin Assembly and DisassemblyHistonesHumansNucleosomesRNA Polymerase IIChromatinDNA-Binding ProteinsHigh Mobility Group ProteinsHistonesNucleosomesRNA Polymerase IITranscriptional Elongation Factors

Identifiers

PMID41028835
PMCPMC12611769

What OpenQuestion holds

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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.