Evidence map›Paper›PMID 27379389›Full record

ArticlePLoS genetics2016

Regulation of the BMP Signaling-Responsive Transcriptional Network in the Drosophila Embryo.

Lisa Deignan, Marco T Pinheiro, Catherine Sutcliffe, Abbie Saunders, Scott G Wilcockson, Leo A H Zeef, Ian J Donaldson, Hilary L Ashe

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Genome-wide analysis of Smad and Schnurri transcription factors inbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. How two extraembryonic epithelia became one: serosa and amnion features and functions ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. BMP Signaling: Lighting up the Way for Embryonic Dorsoventral Patterning.Frontiers in cell and developmental biology · 2021
    Review
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Lisa DeignanFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Marco T PinheiroFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Catherine SutcliffeFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Abbie SaundersFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Scott G WilcocksonFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Leo A H ZeefFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Ian J DonaldsonFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Hilary L AsheFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
University of Manchester · GB

Funding

Medical Research Council MR/M008908/1Wellcome Trust
6 · The paper itself

Abstract

The BMP signaling pathway has a conserved role in dorsal-ventral axis patterning during embryonic development. In Drosophila, graded BMP signaling is transduced by the Mad transcription factor and opposed by the Brinker repressor. In this study, using the Drosophila embryo as a model, we combine RNA-seq with Mad and Brinker ChIP-seq to decipher the BMP-responsive transcriptional network underpinning differentiation of the dorsal ectoderm during dorsal-ventral axis patterning. We identify multiple new BMP target genes, including positive and negative regulators of EGF signaling. Manipulation of EGF signaling levels by loss- and gain-of-function studies reveals that EGF signaling negatively regulates embryonic BMP-responsive transcription. Therefore, the BMP gene network has a self-regulating property in that it establishes a balance between its activity and that of the antagonistic EGF signaling pathway to facilitate correct patterning. In terms of BMP-dependent transcription, we identify key roles for the Zelda and Zerknüllt transcription factors in establishing the resulting expression domain, and find widespread binding of insulator proteins to the Mad and Brinker-bound genomic regions. Analysis of embryos lacking the BEAF-32 insulator protein shows reduced transcription of a peak BMP target gene and a reduction in the number of amnioserosa cells, the fate specified by peak BMP signaling. We incorporate our findings into a model for Mad-dependent activation, and discuss its relevance to BMP signal interpretation in vertebrates.

Indexed as

AnimalsBody PatterningBone Morphogenetic ProteinsDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEmbryonic DevelopmentEmbryo, NonmammalianEpidermal Growth FactorEye ProteinsGene Expression Regulation, DevelopmentalGene Regulatory NetworksHomeodomain ProteinsNuclear ProteinsRepressor ProteinsSignal TransductionBEAF-32 protein, DrosophilaBone Morphogenetic Proteinsbrk protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsEpidermal Growth FactorEye ProteinsHomeodomain ProteinsMAD protein, DrosophilaNuclear ProteinsRepressor ProteinsTranscription FactorsZen protein, Drosophilazld protein, Drosophila

Identifiers

PMID27379389
PMCPMC4933369
OpenAlexW2469664870

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.