Evidence map›Paper›PMID 26647185›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Inositol phosphate kinase 2 is required for imaginal disc development in Drosophila.

Andrew M Seeds, Marco M Tsui, Christine Sunu, Eric P Spana, John D York

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. IPMK depletion influences genome-wide DNA methylation.Biochemical and biophysical research communications · 2025
    Article
  5. bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Review
  8. Inositol in Disease and Development: Roles of Catabolism viaInternational journal of molecular sciences · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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 3 institutions in 1 country.

Andrew M SeedsDepartment of Pharmacology and Cancer Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710;
Marco M TsuiDepartment of Pharmacology and Cancer Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710;
Christine SunuDepartment of Pharmacology and Cancer Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710;
Eric P SpanaDepartment of Biology, Duke University, Durham, NC 27708;
John D YorkDepartment of Pharmacology and Cancer Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710; Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232 john.york@vanderbilt.edu.
Duke University Hospital · USDuke University · USHoward Hughes Medical Institute · US

Funding

The Role of Inositol Signaling in Human DiseaseR01HL055672 · NHLBI · WASHINGTON UNIVERSITY · PI YORK, JOHN D. · 1996 to 2012
$5.4M
Howard Hughes Medical InstituteNHLBI NIH HHS HL-55672NHLBI NIH HHS R01 HL055672
6 · The paper itself

Abstract

Inositol phosphate kinase 2 (Ipk2), also known as IP multikinase IPMK, is an evolutionarily conserved protein that initiates production of inositol phosphate intracellular messengers (IPs), which are critical for regulating nuclear and cytoplasmic processes. Here we report that Ipk2 kinase activity is required for the development of the adult fruit fly epidermis. Ipk2 mutants show impaired development of their imaginal discs, the primordial tissues that form the adult epidermis. Although disk tissue seems to specify normally during early embryogenesis, loss of Ipk2 activity results in increased apoptosis and impairment of proliferation during larval and pupal development. The proliferation defect is in part attributed to a reduction in JAK/STAT signaling, possibly by controlling production or secretion of the pathway's activating ligand, Unpaired. Constitutive activation of the JAK/STAT pathway downstream of Unpaired partially rescues the disk growth defects in Ipk2 mutants. Thus, IP production is essential for proliferation of the imaginal discs, in part, by regulating JAK/STAT signaling. Our work demonstrates an essential role for Ipk2 in producing inositide messengers required for imaginal disk tissue maturation and subsequent formation of adult body structures and provides molecular insights to signaling pathways involved in tissue growth and stability during development.

Indexed as

AnimalsCell ProliferationDrosophila melanogasterDrosophila ProteinsImaginal DiscsJanus KinasesPhosphotransferases (Alcohol Group Acceptor)Signal TransductionSTAT Transcription FactorsTranscription FactorsDrosophila Proteinshop protein, DrosophilaIpk2 protein, DrosophilaJanus KinasesPhosphotransferases (Alcohol Group Acceptor)STAT Transcription FactorsTranscription Factorsinositol phosphate multikinaseinositol phosphatesIpk2IPMKUpd

Identifiers

PMID26647185
PMCPMC4697392
OpenAlexW2204481459

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.