Evidence map›Paper›PMID 23173097›Full record

ArticleG3 (Bethesda, Md.)2012

Evidence for autoregulation and cell signaling pathway regulation from genome-wide binding of the Drosophila retinoblastoma protein.

Pankaj Acharya, Nicolas Negre, John Johnston, Yiliang Wei, Kevin P White, R William Henry, David N Arnosti

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Selective repression of the Drosophila cyclin B promoter by retinoblastoma and E2F proteins.Biochimica et biophysica acta. Gene regulatory mechanisms · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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 2 institutions in 1 country.

Pankaj AcharyaDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824-1319, USA.
Nicolas Negre
John Johnston
Yiliang Wei
Kevin P White
R William Henry
David N Arnosti
Michigan State University · USUniversity of Chicago · US

Funding

A Cis Regulatory map of the Drosophila GenomeU01HG004264 · NHGRI · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2007 to 2011
$12.1M
Analysis of the COP9 signalosome for Retinoblastoma functionR01GM079098 · NIGMS · MICHIGAN STATE UNIVERSITY · PI ARNOSTI, DAVID N · 2007 to 2010
$1.1M
NHGRI NIH HHS U01 HG004264NHGRI NIH HHS U01HG004264NIGMS NIH HHS GM079098NIGMS NIH HHS R01 GM079098
6 · The paper itself

Abstract

The retinoblastoma (RB) tumor suppressor protein is a transcriptional cofactor with essential roles in cell cycle and development. Physical and functional targets of RB and its paralogs p107/p130 have been studied largely in cultured cells, but the full biological context of this family of proteins' activities will likely be revealed only in whole organismal studies. To identify direct targets of the major Drosophila RB counterpart in a developmental context, we carried out ChIP-Seq analysis of Rbf1 in the embryo. The association of the protein with promoters is developmentally controlled; early promoter access is globally inhibited, whereas later in development Rbf1 is found to associate with promoter-proximal regions of approximately 2000 genes. In addition to conserved cell-cycle-related genes, a wholly unexpected finding was that Rbf1 targets many components of the insulin, Hippo, JAK/STAT, Notch, and other conserved signaling pathways. Rbf1 may thus directly affect output of these essential growth-control and differentiation pathways by regulation of expression of receptors, kinases and downstream effectors. Rbf1 was also found to target multiple levels of its own regulatory hierarchy. Bioinformatic analysis indicates that different classes of genes exhibit distinct constellations of motifs associated with the Rbf1-bound regions, suggesting that the context of Rbf1 recruitment may vary within the Rbf1 regulon. Many of these targeted genes are bound by Rbf1 homologs in human cells, indicating that a conserved role of RB proteins may be to adjust the set point of interlinked signaling networks essential for growth and development.

Indexed as

Gene Expression Regulation, DevelopmentalGenome, InsectTranscription, GeneticAnimalsDrosophila melanogasterDrosophila ProteinsGenes, cdcGenes, DevelopmentalHomeostasisNucleotide MotifsPromoter Regions, GeneticProtein BindingRegulonRetinoblastoma ProteinSignal TransductionTranscription FactorsDrosophila ProteinsRbf protein, DrosophilaRetinoblastoma ProteinTranscription Factorscell-cycleDrosophilaRbf1retinoblastoma

Identifiers

PMID23173097
PMCPMC3484676
OpenAlexW2081267078

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.