Evidence map›Paper›PMID 37182209›Full record

ArticleCell reports2023

Regulatory architecture of housekeeping genes is driven by promoter assemblies.

Marion Dejosez, Alessandra Dall'Agnese, Mahesh Ramamoorthy, Jesse Platt, Xing Yin, Megan Hogan, Ran Brosh, Abraham S Weintraub, Denes Hnisz, Brian J Abraham and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Current Challenges of Transcription Compartmentalization Research.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Roles of transposable elements and DNA methylation in the formation of CpG islands and CpG-depleted regulatory elements.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Transcription regulation by biomolecular condensates.Nature reviews. Molecular cell biology · 2025
    Review
  19. Liquid condensates: a new barrier to loop extrusion?Cellular and molecular life sciences : CMLS · 2025
    Review
  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

12 authors at 5 institutions in 1 country.

Marion DejosezBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA.
Alessandra Dall'AgneseWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Mahesh RamamoorthyBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA.
Jesse PlattWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Xing YinBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA.
Megan HoganBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA.
Ran BroshBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA.
Abraham S WeintraubWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Denes HniszWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Brian J AbrahamSt. Jude Research Children's Hospital, Memphis, TN 38105, USA.
Richard A YoungWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA. Electronic address: young@wi.mit.edu.
Thomas P ZwakaBlack Family Stem Cell Institute, Huffington Center for Cell-based Research in Parkinson's Disease, Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10502, USA. Electronic address: thomas.zwaka@mssm.edu.
Icahn School of Medicine at Mount Sinai · USWhitehead Institute for Biomedical Research · USMassachusetts Institute of Technology · USNew York Stem Cell Foundation · USSt. Jude Children's Research Hospital · US

Funding

The Role of p53 in Human Embryonic Stem CellsP01GM081627 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI GOODELL, MARGARET A. · 2007 to 2011
$9.9M
Transcriptional regulation in mammalian cellsR35GM144283 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI RICHARD YOUNG · 2022 to 2026
$4.0M
An inquiry into the function of Ronin in embryogenesis and pluripotent stem cellsR01GM129329 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZWAKA, THOMAS P. · 2018 to 2021
$1.9M
Protection of early embryogenesis and pluripotent stem cells against genetic parasites through a primitive immune systemR01HD100518 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZWAKA, THOMAS P. · 2020 to 2024
$1.7M
Zeiss LSM 980 with Airyscan 2 confocal microscope systemS10OD028520 · OD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI CHEESEMAN, IAIN MCPHERSON · 2021 to 2021
$600k
NICHD NIH HHS R01 HD100518NIGMS NIH HHS P01 GM081627NIGMS NIH HHS R01 GM129329NIGMS NIH HHS R35 GM144283NIH HHS S10 OD028520
6 · The paper itself

Abstract

Genes that are key to cell identity are generally regulated by cell-type-specific enhancer elements bound by transcription factors, some of which facilitate looping to distant gene promoters. In contrast, genes that encode housekeeping functions, whose regulation is essential for normal cell metabolism and growth, generally lack interactions with distal enhancers. We find that Ronin (Thap11) assembles multiple promoters of housekeeping and metabolic genes to regulate gene expression. This behavior is analogous to how enhancers are brought together with promoters to regulate cell identity genes. Thus, Ronin-dependent promoter assemblies provide a mechanism to explain why housekeeping genes can forgo distal enhancer elements and why Ronin is important for cellular metabolism and growth control. We propose that clustering of regulatory elements is a mechanism common to cell identity and housekeeping genes but is accomplished by different factors binding distinct control elements to establish enhancer-promoter or promoter-promoter interactions, respectively.

Indexed as

Enhancer Elements, GeneticGenes, EssentialPromoter Regions, GeneticTranscription FactorsTranscription FactorsCP: Molecular biologyDNA loopingdomesticationembryonic stem cellsgenome organizationP elementpromoter-promoter interactionronintranscriptional regulationtransposon

Identifiers

PMID37182209
PMCPMC10329844
OpenAlexW4376269637

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.