Evidence map›Paper›PMID 24953653›Full record

ArticleCell reports2014

GPS2/KDM4A pioneering activity regulates promoter-specific recruitment of PPARγ.

M Dafne Cardamone, Bogdan Tanasa, Michelle Chan, Carly T Cederquist, Jaclyn Andricovich, Michael G Rosenfeld, Valentina Perissi

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  9. Epigenetic regulation of inflammatory factors in adipose tissue.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2021
    Review
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  17. The Beige Adipocyte as a Therapy for Metabolic Diseases.International journal of molecular sciences · 2019
    Review
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  19. Review
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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

7 authors at 2 institutions in 1 country.

M Dafne CardamoneBiochemistry Department, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Bogdan TanasaDepartment of Medicine, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Michelle ChanBiochemistry Department, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Carly T CederquistBiochemistry Department, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Jaclyn AndricovichBiochemistry Department, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Michael G RosenfeldDepartment of Medicine, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA; Howard Hughes Medical Institute, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Valentina PerissiBiochemistry Department, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA. Electronic address: vperissi@bu.edu.
Boston University · USUniversity of California, San Diego · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
Transcriptional Genomics CoreP01DK074868 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ROSENFELD, M · 2007 to 2016
$16.6M
Ubiquitin-dependent regulation of inflammation and insulin resistanceR01DK100422 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PERISSI, VALENTINA · 2014 to 2018
$1.8M
Role of the NCoR corepressor complex in the development of insulin resistanceR00DK078756 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PERISSI, VALENTINA · 2010 to 2012
$738k
Role of the NCoR corepressor complex in the development of insulin resistanceK99DK078756 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PERISSI, VALENTINA · 2007 to 2008
$171k
NIDDK NIH HHS DK078756NIDDK NIH HHS DK100422NIDDK NIH HHS K99 DK078756NIDDK NIH HHS P01 DK074868NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R00 DK078756NIDDK NIH HHS R01 DK100422
6 · The paper itself

Abstract

Timely and selective recruitment of transcription factors to their appropriate DNA-binding sites represents a critical step in regulating gene activation; however, the regulatory strategies underlying each factor's effective recruitment to specific promoter and/or enhancer regions are not fully understood. Here, we identify an unexpected regulatory mechanism by which promoter-specific binding, and therefore function, of peroxisome proliferator-activator receptor γ (PPARγ) in adipocytes requires G protein suppressor 2 (GPS2) to prime the local chromatin environment via inhibition of the ubiquitin ligase RNF8 and stabilization of the H3K9 histone demethylase KDM4A/JMJD2. Integration of genome-wide profiling data indicates that the pioneering activity of GPS2/KDM4A is required for PPARγ-mediated regulation of a specific transcriptional program, including the lipolytic enzymes adipose triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL). Hence, our findings reveal that GPS2 exerts a biologically important function in adipose tissue lipid mobilization by directly regulating ubiquitin signaling and indirectly modulating chromatin remodeling to prime selected genes for activation.

Indexed as

Promoter Regions, GeneticAcyltransferasesAdipocytesAnimalsChromatin Assembly and DisassemblyHistone DemethylasesIntracellular Signaling Peptides and ProteinsLipaseLipolysisMicePPAR gammaSterol EsteraseUbiquitin-Protein LigasesAcyltransferasesGPS2 protein, mouseHistone DemethylasesIntracellular Signaling Peptides and ProteinsJMJD2A protein, mouseLipasePNPLA2 protein, mousePPAR gammaRnf8 protein, mouseSterol EsteraseUbiquitin-Protein Ligases

Identifiers

PMID24953653
PMCPMC4104678
OpenAlexW2015508531

What OpenQuestion holds

Textmetadata
LicenceTDM
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.