Evidence map›Paper›PMID 35484250›Full record

ArticleNature cell biology2022

NANOG prion-like assembly mediates DNA bridging to facilitate chromatin reorganization and activation of pluripotency.

Kyoung-Jae Choi, My Diem Quan, Chuangye Qi, Joo-Hyung Lee, Phoebe S Tsoi, Mahla Zahabiyon, Aleksandar Bajic, Liya Hu, B V Venkataram Prasad, Shih-Chu Jeff Liao and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Nature cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Transcriptional condensates encode a "golden mean" to optimize enhancer-promoter communication across genomic distances.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. The Biological Function of Genome Organization.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Transcription regulation by biomolecular condensates.Nature reviews. Molecular cell biology · 2025
    Review
  14. Article
  15. Liquid condensates: a new barrier to loop extrusion?Cellular and molecular life sciences : CMLS · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 4 institutions in 1 country.

Kyoung-Jae Choi *Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0001-9541-4182
My Diem Quan *Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX, USA.
Chuangye Qi *Department of Biochemistry and Molecular Biology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA.
Joo-Hyung LeeDepartment of Biochemistry and Molecular Biology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA.
Phoebe S TsoiDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX, USA.
Mahla ZahabiyonDepartment of Molecular and Human Genetics, Baylor College of Medicine and Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
Aleksandar BajicDepartment of Molecular and Human Genetics, Baylor College of Medicine and Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
Liya HuVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-8340-8911
B V Venkataram PrasadVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-1172-2071
Shih-Chu Jeff LiaoISS, Inc., Champaign, IL, USA.
Wenbo LiDepartment of Biochemistry and Molecular Biology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA. Wenbo.Li@uth.tmc.edu.ORCID 0000-0002-9042-5664
Allan Chris M FerreonDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX, USA. Allan.Ferreon@bcm.edu.ORCID 0000-0002-8538-1732
Josephine C FerreonDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX, USA. Josephine.Ferreon@bcm.edu.
Baylor College of Medicine · USThe University of Texas Health Science Center at Houston · USInstitute of Semitic Studies · USThe University of Texas MD Anderson Cancer Center · US

Funding

Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MIRJANA MALETIC-SAVATIC · 2020 to 2026
$9.9M
Structure and Functionof Nanog in Stem Cell PluripotencyR01GM122763 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI Josephine Chu Ferreon · 2018 to 2026
$3.4M
Beyond Gene Dosage: Understanding Down Syndrome via 4D Genome OrganizationU01HL156059 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, WENBO · 2020 to 2024
$3.1M
Phase Transition-Mediated Tau Function and DysfunctionR01NS105874 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI FERREON, ALLAN CHRIS · 2019 to 2023
$2.0M
Mechanisms Underlying Enhancer Rnp Mediated Gene Regulation And Genome OrganizationR01GM136922 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, WENBO · 2020 to 2024
$2.0M
Pharmacologic inhibition of ribonucleoprotein droplet maturationR21NS109678 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI FERREON, ALLAN CHRIS · 2019 to 2019
$440k
Mechanism of Pathologic hnRNP Droplet MaturationR21NS107792 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI FERREON, ALLAN CHRIS · 2019 to 2019
$439k
Optogenetic Engineering of 3D Chromatin ArchitectureR21GM132778 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, WENBO · 2019 to 2020
$434k
NHLBI NIH HHS U01 HL156059NICHD NIH HHS P50 HD103555NIGMS NIH HHS R01 GM122763NIGMS NIH HHS R01 GM136922NIGMS NIH HHS R21 GM132778NINDS NIH HHS R01 NS105874NINDS NIH HHS R21 NS107792NINDS NIH HHS R21 NS109678
6 · The paper itself

Abstract

Human NANOG expression resets stem cells to ground-state pluripotency. Here we identify the unique features of human NANOG that relate to its dose-sensitive function as a master transcription factor. NANOG is largely disordered, with a C-terminal prion-like domain that phase-transitions to gel-like condensates. Full-length NANOG readily forms higher-order oligomers at low nanomolar concentrations, orders of magnitude lower than typical amyloids. Using single-molecule Förster resonance energy transfer and fluorescence cross-correlation techniques, we show that NANOG oligomerization is essential for bridging DNA elements in vitro. Using chromatin immunoprecipitation sequencing and Hi-C 3.0 in cells, we validate that NANOG prion-like domain assembly is essential for specific DNA recognition and distant chromatin interactions. Our results provide a physical basis for the indispensable role of NANOG in shaping the pluripotent genome. NANOG's unique ability to form prion-like assemblies could provide a cooperative and concerted DNA bridging mechanism that is essential for chromatin reorganization and dose-sensitive activation of ground-state pluripotency.

Indexed as

ChromatinPrionsDNAHumansNanog Homeobox ProteinChromatinDNANanog Homeobox ProteinNANOG protein, humanPrions

Identifiers

PMID35484250
PMCPMC9106587
OpenAlexW4225135297

What OpenQuestion holds

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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.