Evidence map›Paper›PMID 25384974›Full record

ArticleMolecular and cellular biology2015

Protein O-fucosyltransferase 1 expression impacts myogenic C2C12 cell commitment via the Notch signaling pathway.

Audrey Der Vartanian, Aymeric Audfray, Bilal Al Jaam, Mathilde Janot, Sébastien Legardinier, Abderrahman Maftah, Agnès Germot

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Article
  9. Current Thoughts of Notch's Role in Myoblast Regulation and Muscle-Associated Disease.International journal of environmental research and public health · 2021
    Review
  10. Article
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  12. Article
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  15. Article
  16. Cancers · 2018
    Article
  17. Article
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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 1 institution in 1 country.

Audrey Der VartanianINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Aymeric AudfrayINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Bilal Al JaamINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Mathilde JanotINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Sébastien LegardinierINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Abderrahman MaftahINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France.
Agnès GermotINRA, UMR 1061, Unité de Génétique Moléculaire Animale, Université de Limoges, Faculté des Sciences et Techniques, Limoges, France agnes.germot@unilim.fr.
Université de Limoges · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch signaling pathway plays a crucial role in skeletal muscle regeneration in mammals by controlling the transition of satellite cells from quiescence to an activated state, their proliferation, and their commitment toward myotubes or self-renewal. O-fucosylation on Notch receptor epidermal growth factor (EGF)-like repeats is catalyzed by the protein O-fucosyltransferase 1 (Pofut1) and primarily controls Notch interaction with its ligands. To approach the role of O-fucosylation in myogenesis, we analyzed a murine myoblastic C2C12 cell line downregulated for Pofut1 expression by short hairpin RNA (shRNA) inhibition during the time course of differentiation. Knockdown of Pofut1 affected the signaling pathway activation by a reduction of the amount of cleaved Notch intracellular domain and a decrease in downstream Notch target gene expression. Depletion in Pax7(+)/MyoD(-) cells and earlier myogenic program entrance were observed, leading to an increase in myotube quantity with a small number of nuclei, reflecting fusion defects. The rescue of Pofut1 expression in knockdown cells restored Notch signaling activation and a normal course in C2C12 differentiation. Our results establish the critical role of Pofut1 on Notch pathway activation during myogenic differentiation.

Indexed as

AnimalsCell DifferentiationCell LineFucosyltransferasesGene Knockdown TechniquesMiceMuscle DevelopmentMyoblastsPAX7 Transcription FactorReceptors, NotchSignal TransductionFucosyltransferasesPax7 protein, mousePAX7 Transcription FactorPofut1 protein, mouseReceptors, Notch

Identifiers

PMID25384974
PMCPMC4272425
OpenAlexW2161867630

What OpenQuestion holds

Textmetadata
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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.