Evidence map›Paper›PMID 24891619›Full record

ArticleMolecular and cellular biology2014

RNA-binding protein AUF1 promotes myogenesis by regulating MEF2C expression levels.

Amaresh C Panda, Kotb Abdelmohsen, Je-Hyun Yoon, Jennifer L Martindale, Xiaoling Yang, Jessica Curtis, Evi M Mercken, Devon M Chenette, Yongqing Zhang, Robert J Schneider and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

40 citing papers in PubMed, 58 citations in OpenAlex.

  1. ReducedbioRxiv : the preprint server for biology · 2026
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  11. RNA binding proteins as mediators of pathological cardiac remodeling.Frontiers in cell and developmental biology · 2024
    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

13 authors at 2 institutions in 1 country.

Amaresh C PandaLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Kotb AbdelmohsenLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Je-Hyun YoonLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Jennifer L MartindaleLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Xiaoling YangLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Jessica CurtisTranslational Gerontology Branch, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Evi M MerckenTranslational Gerontology Branch, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Devon M ChenetteDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Yongqing ZhangLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Robert J SchneiderDepartment of Microbiology, New York University School of Medicine, New York, New York, USA.
Kevin G BeckerLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Rafael de CaboTranslational Gerontology Branch, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA.
Myriam GorospeLaboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, Maryland, USA myriam-gorospe@nih.gov.
National Institutes of Health · USNew York University · US

Funding

Post-transcriptional Regulation Of Proliferative and Stress Response GenesZIAAG000511 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$25.4M
Post-transcriptional regulation of energy usage: glucose and lipid metabolismZIAAG000394 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$18.7M
Analysis of complex biological systems by microarray based gene expressionZICAG000616 · NIA · NATIONAL INSTITUTE ON AGING · PI DE, SUPRIYO · 2009 to 2025
$15.5M
Ionizing Radiation Control of Inflammatory Cytokine mRNA Stability and ExpressionR01GM085693 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHNEIDER, ROBERT JAY · 2009 to 2013
$1.7M
Total Synthesis of the Adjuvant Saponin Jujuboside AF32GM090476 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI COWEN, BRYAN JAMES · 2010 to 2011
$99k
Intramural NIH HHSNIGMS NIH HHS GM085693NIGMS NIH HHS R01 GM085693NIGMS NIH HHS T32 GM13-A0-S1-090476
6 · The paper itself

Abstract

The mammalian RNA-binding protein AUF1 (AU-binding factor 1, also known as heterogeneous nuclear ribonucleoprotein D [hnRNP D]) binds to numerous mRNAs and influences their posttranscriptional fate. Given that many AUF1 target mRNAs encode muscle-specific factors, we investigated the function of AUF1 in skeletal muscle differentiation. In mouse C2C12 myocytes, where AUF1 levels rise at the onset of myogenesis and remain elevated throughout myocyte differentiation into myotubes, RNP immunoprecipitation (RIP) analysis indicated that AUF1 binds prominently to Mef2c (myocyte enhancer factor 2c) mRNA, which encodes the key myogenic transcription factor MEF2C. By performing mRNA half-life measurements and polysome distribution analysis, we found that AUF1 associated with the 3' untranslated region (UTR) of Mef2c mRNA and promoted MEF2C translation without affecting Mef2c mRNA stability. In addition, AUF1 promoted Mef2c gene transcription via a lesser-known role of AUF1 in transcriptional regulation. Importantly, lowering AUF1 delayed myogenesis, while ectopically restoring MEF2C expression levels partially rescued the impairment of myogenesis seen after reducing AUF1 levels. We propose that MEF2C is a key effector of the myogenesis program promoted by AUF1.

Indexed as

3' Untranslated RegionsAnimalsCell DifferentiationCell LineGene Expression Regulation, DevelopmentalHeterogeneous-Nuclear Ribonucleoprotein DHeterogeneous Nuclear Ribonucleoprotein D0MEF2 Transcription FactorsMiceMice, Inbred C57BLMuscle DevelopmentMuscle Fibers, SkeletalMuscle, SkeletalProtein BindingProtein BiosynthesisRegeneration3' Untranslated RegionsHeterogeneous-Nuclear Ribonucleoprotein DHeterogeneous Nuclear Ribonucleoprotein D0Hnrpd protein, mouseMef2c protein, mouseMEF2 Transcription FactorsRNA-Binding ProteinsRNA, MessengerRNA, Small Interfering

Identifiers

PMID24891619
PMCPMC4135590
OpenAlexW2122206493

What OpenQuestion holds

Textmetadata
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.