Evidence map›Paper›PMID 30742616›Full record

ArticlePLoS biology2019

Developmental regulation of regenerative potential in Drosophila by ecdysone through a bistable loop of ZBTB transcription factors.

Karine Narbonne-Reveau, Cédric Maurange

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. E93 controls adult differentiation by repressingProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Chronologically inappropriate morphogenesis (Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Steroid signaling controls sex-specific development in an invertebrate.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Frontiers in cell and developmental biology · 2024
    Review
  12. Article
  13. Article
  14. The remodeling of Z-DNA in the mammalian germ line.Biochemical Society transactions · 2022
    Article
  15. Imaginal Disc Regeneration: Something Old, Something New.Cold Spring Harbor perspectives in biology · 2022
    Review
  16. Article
  17. A transcription factor that enables metamorphosis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. The wing imaginal disc.Genetics · 2022
    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

2 authors at 1 institution in 1 country.

Karine Narbonne-ReveauAix Marseille Université, CNRS, IBDM, UMR 7288, Marseille, France.
Cédric MaurangeAix Marseille Université, CNRS, IBDM, UMR 7288, Marseille, France.ORCID 0000-0001-8931-1419
Centre National de la Recherche Scientifique · FR

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
NIGMS NIH HHS R01 GM084947NIH HHS P40 OD018537
6 · The paper itself

Abstract

In many organisms, the regenerative capacity of tissues progressively decreases as development progresses. However, the developmental mechanisms that restrict regenerative potential remain unclear. In Drosophila, wing imaginal discs become unable to regenerate upon damage during the third larval stage (L3). Here, we show that production of ecdysone after larvae reach their critical weight (CW) terminates the window of regenerative potential by acting on a bistable loop composed of two antagonistic Broad-complex/Tramtrack/Bric-à-brac Zinc-finger (ZBTB) genes: chinmo and broad (br). Around mid L3, ecdysone signaling silences chinmo and activates br to switch wing epithelial progenitors from a default self-renewing to a differentiation-prone state. Before mid L3, Chinmo promotes a strong regenerative response upon tissue damage. After mid L3, Br installs a nonpermissive state that represses regeneration. Transient down-regulation of ecdysone signaling or Br in late L3 larvae enhances chinmo expression in damaged cells that regain the capacity to regenerate. This work unveils a mechanism that ties the self-renewing and regenerative potential of epithelial progenitors to developmental progression.

Indexed as

AgingAnimalsDrosophila melanogasterDrosophila ProteinsEcdysoneEpithelial CellsGene Expression Regulation, DevelopmentalImaginal DiscsLarvaNerve Tissue ProteinsRegenerationSignal TransductionStem CellsTranscription FactorsWings, AnimalBr protein, DrosophilaChinmo protein, DrosophilaDrosophila ProteinsEcdysoneNerve Tissue ProteinsTranscription Factors

Identifiers

PMID30742616
PMCPMC6386533
OpenAlexW2912110157

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.