Evidence map›Paper›PMID 23987512›Full record

ArticleDevelopmental cell2013

A multifunctional protein, EWS, is essential for early brown fat lineage determination.

Jun Hong Park, Hong Jun Kang, Soo Im Kang, Ji Eun Lee, Jamie Hur, Kai Ge, Elisabetta Mueller, Hongjie Li, Byeong-Chel Lee, Sean Bong Lee

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

48 citing papers in PubMed, 82 citations in OpenAlex.

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  12. Signaling Pathways Regulating Thermogenesis.Frontiers in endocrinology · 2021
    Review
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  17. KMT5c modulates adipocyte thermogenesis by regulatingProceedings of the National Academy of Sciences of the United States of America · 2020
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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

10 authors at 3 institutions in 1 country.

Jun Hong ParkGenetics of Development and Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases, 9000 Rockville Pike, Bethesda, MD 20892, USA.
Hong Jun Kang
Soo Im Kang
Ji Eun Lee
Jamie Hur
Kai Ge
Elisabetta Mueller
Hongjie Li
Byeong-Chel Lee
Sean Bong Lee
National Institute of Diabetes and Digestive and Kidney Diseases · USTulane University · USUPMC Hillman Cancer Center · US

Funding

Regulation of PPARgamma Expression and Adipogenesis by PTIP-Associated FactorsZIADK075003 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GE, KAI · 2009 to 2025
$17.6M
Epigenomic Regulation of PPARgamma and AdipogenesisZIADK075017 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GE, KAI · 2009 to 2025
$12.4M
Identification of novel transcriptional regulators of lipid metabolism.ZIADK056023 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI MUELLER, ELISABETTA · 2009 to 2016
$3.9M
Identification of novel molecules and pathways that modulate adipogenesisZIADK075004 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI MUELLER, ELISABETTA · 2009 to 2016
$3.9M
Epigenomic Regulation of Nuclear Receptor Target Gene ExpressionZIADK047055 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GE, KAI · 2009 to 2017
$2.3M
Physiological roles of Ewings Sarcoma gene product EWSZIADK056005 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEE, SEAN · 2009 to 2012
$1.7M
Intramural NIH HHS ZIA DK056005
6 · The paper itself

Abstract

The recent surge in obesity has provided an impetus to better understand the mechanisms of adipogenesis, particularly in brown adipose tissue (BAT) because of its potential utilization for antiobesity therapy. Postnatal brown adipocytes arise from early muscle progenitors, but how brown fat lineage is determined is not completely understood. Here, we show that a multifunctional protein, Ewing Sarcoma (EWS), is essential for determining brown fat lineage during development. BATs from Ews null embryos and newborns are developmentally arrested. Ews mutant brown preadipocytes fail to differentiate due to loss of Bmp7 expression, a critical early brown adipogenic factor. We demonstrate that EWS, along with its binding partner Y-box binding protein 1 (YBX1), activates Bmp7 transcription. Depletion of either Ews or Ybx1 leads to loss of Bmp7 expression and brown adipogenesis. Remarkably, Ews null BATs and brown preadipocytes ectopically express myogenic genes. These results demonstrate that EWS is essential for early brown fat lineage determination.

Indexed as

Adipocytes, BrownAdipogenesisAdipose Tissue, BrownAnimalsBone Morphogenetic Protein 7Cell DifferentiationCell LineCold TemperatureDiet, High-FatEmbryo, MammalianGene Expression Regulation, DevelopmentalGenetic Complementation TestHumansMiceMultiprotein ComplexesMuscle DevelopmentBone Morphogenetic Protein 7Multiprotein ComplexesRNA-Binding Protein EWSTranscription FactorsYbx1 protein, mouse

Identifiers

PMID23987512
PMCPMC3817832
OpenAlexW1970412343

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.