Evidence map›Paper›PMID 26823289›Full record

ArticleNature communications2016

E2F function in muscle growth is necessary and sufficient for viability in Drosophila.

Maria Paula Zappia, Maxim V Frolov

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  6. Large Yellow Croaker (International journal of molecular sciences · 2025
    Article
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  11. Postsynaptic BMP signaling regulates myonuclear properties inbioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. Article
  14. E2F regulation of theProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. 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

2 authors at 1 institution in 1 country.

Maria Paula ZappiaDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, 900 S Ashland Avenue, Chicago, Illinois 60607, USA.
Maxim V FrolovDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, 900 S Ashland Avenue, Chicago, Illinois 60607, USA.
Ashland (United States) · US

Funding

Rb and Hippo tumor suppressor pathways in differentiationR01GM093827 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FROLOV, MAXIM · 2011 to 2018
$2.2M
Functional interaction between the mir11~998 intronic microRNA cluster and Retinoblastoma tumor suppressor pathwayR01GM110018 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FROLOV, MAXIM · 2015 to 2018
$1.3M
NIGMS NIH HHS GM110018NIGMS NIH HHS GM93827NIGMS NIH HHS R01 GM093827NIGMS NIH HHS R01 GM110018
6 · The paper itself

Abstract

The E2F transcription factor is a key cell cycle regulator. However, the inactivation of the entire E2F family in Drosophila is permissive throughout most of animal development until pupation when lethality occurs. Here we show that E2F function in the adult skeletal muscle is essential for animal viability since providing E2F function in muscles rescues the lethality of the whole-body E2F-deficient animals. Muscle-specific loss of E2F results in a significant reduction in muscle mass and thinner myofibrils. We demonstrate that E2F is dispensable for proliferation of muscle progenitor cells, but is required during late myogenesis to directly control the expression of a set of muscle-specific genes. Interestingly, E2f1 provides a major contribution to the regulation of myogenic function, while E2f2 appears to be less important. These findings identify a key function of E2F in skeletal muscle required for animal viability, and illustrate how the cell cycle regulator is repurposed in post-mitotic cells.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsE2F1 Transcription FactorE2F2 Transcription FactorFemaleGene Expression Regulation, DevelopmentalGene Knockdown TechniquesLarvaMaleMuscle DevelopmentMusclesPupaTrans-ActivatorsDp transcription factor, DrosophilaDrosophila ProteinsE2F1 Transcription FactorE2f2 protein, DrosophilaE2F2 Transcription FactorTrans-Activators

Identifiers

PMID26823289
PMCPMC4740182
OpenAlexW2298332800

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.