Evidence map›Paper›PMID 26160905›Full record

ArticleDevelopment (Cambridge, England)2015

Scalloped and Yorkie are required for cell cycle re-entry of quiescent cells after tissue damage.

Joy H Meserve, Robert J Duronio

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. 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
2.8field-weighted citation impact, top 10% 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, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Imaginal Disc Regeneration: Something Old, Something New.Cold Spring Harbor perspectives in biology · 2022
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Polyploidy in tissue homeostasis and regeneration.Development (Cambridge, England) · 2018
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Imaginal disc regeneration takes flight.Current opinion in cell biology · 2017
    Review
  20. Review
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.

Joy H MeserveCurriculum in Genetics & Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Robert J DuronioCurriculum in Genetics & Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA Integrative Program for Biological and Genome Sciences, University of North Carolina, Chapel Hill, NC 27599, USA Departments of Biology and Genetics, University of North Carolina, Chapel Hill, NC 27599, USA Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, USA duronio@med.unc.edu.
University of North Carolina at Chapel Hill · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
HISTONE MRNA REGULATION IN DEVELOPMENTR01GM058921 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DURONIO, ROBERT J, MARZLUFF, WILLIAM F. · 1999 to 2025
$11.6M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
GENETIC ANALYSIS OF E2F FUNCTION DURING DEVELOPMENTR01GM057859 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DURONIO, ROBERT J · 1999 to 2012
$3.5M
Identifying a transcriptional program that regulates compensatory proliferationF31AG044957 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MESERVE, JOY HART · 2013 to 2015
$97k
NIA NIH HHS F31 AG044957NIGMS NIH HHS R01 GM057859NIGMS NIH HHS R01-GM057859NIGMS NIH HHS R01 GM058921NIGMS NIH HHS R01-GM058921NIGMS NIH HHS T32 GM007092NIGMS NIH HHS T32-GM007092NIH HHS P40 OD018537NIH HHS P40OD018537
6 · The paper itself

Abstract

Regeneration of damaged tissues typically requires a population of active stem cells. How damaged tissue is regenerated in quiescent tissues lacking a stem cell population is less well understood. We used a genetic screen in the developing Drosophila melanogaster eye to investigate the mechanisms that trigger quiescent cells to re-enter the cell cycle and proliferate in response to tissue damage. We discovered that Hippo signaling regulates compensatory proliferation after extensive cell death in the developing eye. Scalloped and Yorkie, transcriptional effectors of the Hippo pathway, drive Cyclin E expression to induce cell cycle re-entry in cells that normally remain quiescent in the absence of damage. Ajuba, an upstream regulator of Hippo signaling that functions as a sensor of epithelial integrity, is also required for cell cycle re-entry. Thus, in addition to its well-established role in modulating proliferation during periods of tissue growth, Hippo signaling maintains homeostasis by regulating quiescent cell populations affected by tissue damage.

Indexed as

Animalsbeta-GalactosidaseCell CycleCyclin EDrosophila melanogasterDrosophila ProteinsEyeFemaleHippo KinasesImage Processing, Computer-AssistedIndolesIn Situ Hybridization, FluorescenceIntracellular Signaling Peptides and ProteinsMicroscopy, FluorescenceNuclear ProteinsProtein Serine-Threonine Kinasesbeta-GalactosidaseCyclin EDAPIDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIndolesIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine Kinasessd protein, DrosophilaTrans-ActivatorsTranscription FactorsYAP-Signaling ProteinsYki protein, DrosophilaApoptosisCell cycleCompensatory proliferationDrosophilaHippo signalingQuiescenceRegeneration

Identifiers

PMID26160905
PMCPMC4550963
OpenAlexW2110195338

What OpenQuestion holds

Textmetadata
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.