Evidence map›Paper›PMID 30379844›Full record

ArticlePLoS biology2018

EGFR signaling coordinates patterning with cell survival during Drosophila epidermal development.

Samuel H Crossman, Sebastian J Streichan, Jean-Paul Vincent

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  9. Time and space in segmentation.Interface focus · 2021
    Article
  10. Regulation of size and scale in vertebrate spinal cord development.Wiley interdisciplinary reviews. Developmental biology · 2021
    Review
  11. Article
  12. 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

3 authors at 2 institutions in 2 countries.

Samuel H CrossmanThe Francis Crick Institute, London, United Kingdom.ORCID 0000-0002-3898-4055
Sebastian J StreichanDepartment of Physics, University of California, Santa Barbara, California, United States of America.
Jean-Paul VincentThe Francis Crick Institute, London, United Kingdom.ORCID 0000-0003-2305-5744
The Francis Crick Institute · GBUniversity of California, Santa Barbara · US

Funding

Tissue flow genetics: using cartography to reveal forces driving morphogenesisR00HD088708 · NICHD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI STREICHAN, SEBASTIAN J · 2018 to 2020
$659k
NICHD NIH HHS R00 HD088708Wellcome Trust 206341/Z/17/ZWellcome Trust FC001204
6 · The paper itself

Abstract

Extensive apoptosis is often seen in patterning mutants, suggesting that tissues can detect and eliminate potentially harmful mis-specified cells. Here, we show that the pattern of apoptosis in the embryonic epidermis of Drosophila is not a response to fate mis-specification but can instead be explained by the limiting availability of prosurvival signaling molecules released from locations determined by patterning information. In wild-type embryos, the segmentation cascade elicits the segmental production of several epidermal growth factor receptor (EGFR) ligands, including the transforming growth factor Spitz (TGFα), and the neuregulin, Vein. This leads to an undulating pattern of signaling activity, which prevents expression of the proapoptotic gene head involution defective (hid) throughout the epidermis. In segmentation mutants, where specific peaks of EGFR ligands fail to form, gaps in signaling activity appear, leading to coincident hid up-regulation and subsequent cell death. These data provide a mechanistic understanding of how cell survival, and thus appropriate tissue size, is made contingent on correct patterning.

Indexed as

AnimalsAnimals, Genetically ModifiedApoptosisBody PatterningCell SurvivalDrosophila melanogasterDrosophila ProteinsEpidermal Growth FactorEpidermisErbB ReceptorsFemaleGenes, InsectLigandsMaleMembrane ProteinsMutationDrosophila ProteinsEgfr protein, DrosophilaEpidermal Growth FactorErbB ReceptorsHID protein, DrosophilaLigandsMembrane ProteinsNeuregulinsNeuropeptidesReceptors, Invertebrate Peptidespi protein, Drosophilavn protein, Drosophila

Identifiers

PMID30379844
PMCPMC6231689
OpenAlexW2951610716

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.