Evidence map›Paper›PMID 26819411›Full record

ArticleNucleic acids research2016

Novel RNA-binding activity of MYF5 enhances Ccnd1/Cyclin D1 mRNA translation during myogenesis.

Amaresh C Panda, Kotb Abdelmohsen, Jennifer L Martindale, Clara Di Germanio, Xiaoling Yang, Ioannis Grammatikakis, Ji Heon Noh, Yongqing Zhang, Elin Lehrmann, Dawood B Dudekula and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Foxg1 and companions: Not only transcription factors.Neural regeneration research · 2026
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  4. Transcriptomic analysis of Cr(VI)-induced changes in C2C12 cells during myogenic differentiation.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2025
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  12. Genistein Promotes Skeletal Muscle Regeneration by Regulating miR-221/222.International journal of molecular sciences · 2022
    Article
  13. Article
  14. The synaptosome-associated protein 23 (SNAP23) is necessary for proper myogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  15. Effects of Focused Vibrations on Human Satellite Cells.International journal of molecular sciences · 2022
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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

16 authors at 3 institutions in 2 countries.

Amaresh C PandaLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA amaresh.panda@nih.gov.
Kotb AbdelmohsenLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Jennifer L MartindaleLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Clara Di GermanioTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD 21224, USA Faculty of Veterinary Medicine, University of Teramo, Teramo, Italy.
Xiaoling YangLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Ioannis GrammatikakisLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Ji Heon NohLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Yongqing ZhangLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Elin LehrmannLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Dawood B DudekulaLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Supriyo DeLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Kevin G BeckerLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
Elizabeth J WhiteDepartment of Biochemistry and Molecular Biology and Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Gerald M WilsonDepartment of Biochemistry and Molecular Biology and Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Rafael de CaboTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD 21224, USA.
Myriam GorospeLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD21224, USA.
National Institute on Aging · USUniversity of Maryland, Baltimore · USUniversity of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center

Funding

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
Bioinformatic Analysis of the Genetics of Common Complex DiseasesZICAG000613 · NIA · NATIONAL INSTITUTE ON AGING · PI DE, SUPRIYO · 2010 to 2025
$3.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Skeletal muscle contains long multinucleated and contractile structures known as muscle fibers, which arise from the fusion of myoblasts into multinucleated myotubes during myogenesis. The myogenic regulatory factor (MRF) MYF5 is the earliest to be expressed during myogenesis and functions as a transcription factor in muscle progenitor cells (satellite cells) and myocytes. In mouse C2C12 myocytes, MYF5 is implicated in the initial steps of myoblast differentiation into myotubes. Here, using ribonucleoprotein immunoprecipitation (RIP) analysis, we discovered a novel function for MYF5 as an RNA-binding protein which associated with a subset of myoblast mRNAs. One prominent MYF5 target was Ccnd1 mRNA, which encodes the key cell cycle regulator CCND1 (Cyclin D1). Biotin-RNA pulldown, UV-crosslinking and gel shift experiments indicated that MYF5 was capable of binding the 3' untranslated region (UTR) and the coding region (CR) of Ccnd1 mRNA. Silencing MYF5 expression in proliferating myoblasts revealed that MYF5 promoted CCND1 translation and modestly increased transcription of Ccnd1 mRNA. Accordingly, overexpressing MYF5 in C2C12 cells upregulated CCND1 expression while silencing MYF5 reduced myoblast proliferation as well as differentiation of myoblasts into myotubes. Moreover, MYF5 silencing reduced myogenesis, while ectopically restoring CCND1 abundance partially rescued the decrease in myogenesis seen after MYF5 silencing. We propose that MYF5 enhances early myogenesis in part by coordinately elevating Ccnd1 transcription and Ccnd1 mRNA translation.

Indexed as

AnimalsCell DifferentiationCell LineCell ProliferationCyclin D1Gene Expression ProfilingGene Expression RegulationMiceMicroarray AnalysisMuscle DevelopmentMyoblastsMyogenic Regulatory Factor 5Protein BindingProtein BiosynthesisRecombinant Fusion ProteinsRNA, MessengerCcnd1 protein, mouseCyclin D1Myf5 protein, mouseMyogenic Regulatory Factor 5Recombinant Fusion ProteinsRNA, Messenger

Identifiers

PMID26819411
PMCPMC4797292
OpenAlexW2301925216

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Registered trials

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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.