Evidence map›Paper›PMID 18694568›Full record

ArticleDevelopmental cell2008

Hox and senseless antagonism functions as a molecular switch to regulate EGF secretion in the Drosophila PNS.

David Li-Kroeger, Lorraine M Witt, H Leighton Grimes, Tiffany A Cook, Brian Gebelein

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

42 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Micromanagement ofJournal of developmental biology · 2022
    Review
  3. Mechanisms Underlying Hox-Mediated Transcriptional Outcomes.Frontiers in cell and developmental biology · 2021
    Review
  4. Article
  5. Article
  6. Novel mRNAs 3' end-associatedRNA (New York, N.Y.) · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Regulatory logic driving stable levels ofDevelopment (Cambridge, England) · 2017
    Article
  12. Mechanisms of Specificity for Hox Factor Activity.Journal of developmental biology · 2016
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

5 authors at 1 institution in 1 country.

David Li-KroegerDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Lorraine M Witt
H Leighton Grimes
Tiffany A Cook
Brian Gebelein
Cincinnati Children's Hospital Medical Center · US

Funding

Mechanisms of Homeodomain Transcriptional SpecificityR01GM079428 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI GEBELEIN, BRIAN · 2008 to 2023
$4.5M
NIGMS NIH HHS R01 GM079428PHS HHS RGM079428A
6 · The paper itself

Abstract

Hox factors are key regulators of distinct cells, tissues, and organs along the body plan. However, little is known about how Hox factors regulate cell-specific gene expression to pattern diverse tissues. Here, we show an unexpected Hox transcriptional mechanism: the permissive regulation of EGF secretion, and thereby cell specification, by antagonizing the Senseless transcription factor in the peripheral nervous system. rhomboid expression in a subset of sensory cells stimulates EGF secretion to induce hepatocyte-like cell development. We identified a rhomboid enhancer that is active in these cells and show that an abdominal Hox complex directly competes with Senseless for enhancer binding, with the transcriptional outcome dependent upon their relative binding activities. Thus, Hox-Senseless antagonism forms a molecular switch that integrates neural and anterior-posterior positional information. As the vertebrate senseless homolog is essential for neural development as well as hematopoiesis, we propose Hox-Senseless antagonism will broadly control cell fate decisions.

Indexed as

AbdomenAnimalsBase SequenceBinding SitesConserved SequenceDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEnhancer Elements, GeneticEpidermal Growth FactorGene Expression Regulation, DevelopmentalHomeodomain ProteinsModels, BiologicalMolecular Sequence DataNuclear ProteinsPeripheral Nervous SystemDrosophila ProteinsEpidermal Growth FactorHomeodomain ProteinsNuclear ProteinsrhoA GTP-Binding Proteinsens protein, DrosophilaTranscription Factors

Identifiers

PMID18694568
PMCPMC2610489
OpenAlexW2064751912

What OpenQuestion holds

Textmetadata
LicenceTDM
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.