Evidence map›Paper›PMID 24075010›Full record

ArticleCell2013

MEF2 is an in vivo immune-metabolic switch.

Rebecca I Clark, Sharon W S Tan, Claire B Péan, Urmas Roostalu, Valérie Vivancos, Kévin Bronda, Martina Pilátová, Jingqi Fu, David W Walker, Rebecca Berdeaux and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

90 citing papers in PubMed, 1 synthesis or guideline pooled it, 176 citations in OpenAlex.

  1. Pooled it
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  17. Regulating metabolism to shape immune function: Lessons from Drosophila.Seminars in cell & developmental biology · 2023
    Review
  18. Gene Structure, Expression and Function Analysis ofInternational journal of molecular sciences · 2023
    Article
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Rebecca I ClarkCentre for the Molecular and Cellular Biology of Inflammation and Peter Gorer Department of Immunobiology, King's College London School of Medicine, London SE1 1UL, UK; Department of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Sharon W S Tan
Claire B Péan
Urmas Roostalu
Valérie Vivancos
Kévin Bronda
Martina Pilátová
Jingqi Fu
David W Walker
Rebecca Berdeaux
Frédéric Geissmann
Marc S Dionne
King's College London · GBThe University of Texas Health Science Center at Houston · USUniversity of California, Los Angeles · US

Funding

Role of Mitochondrial Homeostasis in Animal AgingR01AG037514 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI David W Walker · 2010 to 2026
$5.3M
Regulation of glucose utilization by skeletal muscle SIK1R01DK092590 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BERDEAUX, REBECCA L · 2011 to 2021
$3.3M
Metabolic regulation of stem cell behavior and longevityR01AG040288 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE, WALKER, DAVID W · 2012 to 2016
$3.0M
The role of SIK1 in myogenic differentiation and skeletal muscle repairR01AR059847 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BERDEAUX, REBECCA L · 2011 to 2015
$1.7M
Biotechnology and Biological Sciences Research Council BB/E02128X/1Medical Research Council G0900867NIAMS NIH HHS R01 AR059847NIAMS NIH HHS R01AR059847NIA NIH HHS R01 AG037514NIA NIH HHS R01AG037514NIA NIH HHS R01 AG040288NIA NIH HHS R01AG040288NIDDK NIH HHS R01 DK092590NIDDK NIH HHS R01DK092590Wellcome Trust WT085119MA
6 · The paper itself

Abstract

Infections disturb metabolic homeostasis in many contexts, but the underlying connections are not completely understood. To address this, we use paired genetic and computational screens in Drosophila to identify transcriptional regulators of immunity and pathology and their associated target genes and physiologies. We show that Mef2 is required in the fat body for anabolic function and the immune response. Using genetic and biochemical approaches, we find that MEF2 is phosphorylated at a conserved site in healthy flies and promotes expression of lipogenic and glycogenic enzymes. Upon infection, this phosphorylation is lost, and the activity of MEF2 changes--MEF2 now associates with the TATA binding protein to bind a distinct TATA box sequence and promote antimicrobial peptide expression. The loss of phosphorylated MEF2 contributes to loss of anabolic enzyme expression in Gram-negative bacterial infection. MEF2 is thus a critical transcriptional switch in the adult fat body between metabolism and immunity.

Indexed as

Amino Acid SequenceAnimalsCandida albicansDrosophila melanogasterDrosophila ProteinsEnterobacter cloacaeFat BodyGene Expression RegulationGlycogenMetabolismMycobacterium marinumMyogenic Regulatory FactorsPhosphorylationTATA-Box Binding ProteinDrosophila ProteinsGlycogenMef2 protein, DrosophilaMyogenic Regulatory FactorsTATA-Box Binding Protein

Identifiers

PMID24075010
PMCPMC3807682
OpenAlexW2115553685

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.