Evidence map›Paper›PMID 23070566›Full record

ArticleCell cycle (Georgetown, Tex.)2012

Drosophila GAGA factor is required for full activation of the dE2f1-Yki/Sd transcriptional program.

Battuya Bayarmagnai, Brandon N Nicolay, Abul B M M K Islam, Nuria Lopez-Bigas, Maxim V Frolov

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Yorkie/YAP Interactors: Fine-Tuning the Hippo Pathway Output.Cold Spring Harbor perspectives in biology · 2026
    Article
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  7. GAGA factor: a multifunctional pioneering chromatin protein.Cellular and molecular life sciences : CMLS · 2021
    Review
  8. Article
  9. Article
  10. Review
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  12. Article
  13. New insights for Drosophila GAGA factor in larvae.Royal Society open science · 2015
    Article
  14. Article
  15. Article
  16. Temporal regulation of Dpp signaling output in the Drosophila wing.Developmental dynamics : an official publication of the American Association of Anatomists · 2014
    Article
  17. Article
  18. 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

5 authors at 3 institutions in 2 countries.

Battuya BayarmagnaiDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Brandon N Nicolay
Abul B M M K Islam
Nuria Lopez-Bigas
Maxim V Frolov
University of Illinois Chicago · USInstitució Catalana de Recerca i Estudis Avançats · ESUniversitat Pompeu Fabra · ES

Funding

Rb and Hippo tumor suppressor pathways in differentiationR01GM093827 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FROLOV, MAXIM · 2011 to 2018
$2.2M
NIGMS NIH HHS GM93827NIGMS NIH HHS R01 GM093827
6 · The paper itself

Abstract

The Hippo signaling pathway regulates organ size by controlling the activity of the transcriptional co-activator Yorkie (Yki). Yki is recruited to its target genes by DNA-binding proteins such as Scalloped (Sd). In addition, transcription factor dE2f1, of the Retinoblastoma (Rb) pathway, cooperates with Yki/Sd to synergistically activate a set of common cell cycle target genes. However, little is known about other factors that ensure the proper transcriptional output of Hippo signaling. In this report we identified the chromatin protein GAGA factor (GAF), which is encoded by the Trithorax-like (Trl) gene, as a novel and critical partner in transcriptional regulation by Yki/Sd and dE2f1. We show that GAF is required for the full activation of target genes by dE2f1 and Yki/Sd; while ablation of GAF compromises both normal and inappropriate cell proliferation driven by Yki and dE2f1 in multiple tissues. The importance of GAF is further supported by strong genetic interactions between GAF and the Rb and Hippo pathways. Additionally, we show that GAF directly interacts with RBF, a Drosophila pRB homolog, and partially co-localizes with RBF on polytene chromosomes. Collectively, our data provide a novel connection between a chromatin-binding protein and a transcriptional program governed by the Hippo and Rb pathways.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsCell ProliferationDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsE2F1 Transcription FactorHippo KinasesIntracellular Signaling Peptides and ProteinsNuclear ProteinsPromoter Regions, GeneticProtein Serine-Threonine KinasesRNA, Double-StrandedRNA InterferenceSignal TransductionTrans-ActivatorsAdaptor Proteins, Vesicular TransportDNA-Binding ProteinsDrosophila ProteinsE2F1 Transcription FactorHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine KinasesRB protein, DrosophilaRNA, Double-Strandedsd protein, DrosophilaTrans-ActivatorsTranscription FactorsTrl protein, DrosophilaYAP-Signaling ProteinsYki protein, Drosophila

Identifiers

PMID23070566
PMCPMC3524215
OpenAlexW1965198388

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.