Evidence map›Paper›PMID 25395458›Full record

ArticleDevelopment (Cambridge, England)2014

Wnt/β-catenin signaling integrates patterning and metabolism of the insect growth zone.

Georg Oberhofer, Daniela Grossmann, Janna L Siemanowski, Tim Beissbarth, Gregor Bucher

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Temporal control of RNAi reveals both robust and labile feedback loops in the segmentation clock of the red flour beetle.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  2. Article
  3. Review
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  5. Article
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  8. Persistent Parental RNAi in the BeetleAdvanced genetics (Hoboken, N.J.) · 2022
    Article
  9. Silencing ofInternational journal of molecular sciences · 2022
    Article
  10. Review
  11. Time and space in segmentation.Interface focus · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Embryonic expression of priapulid Wnt genes.Development genes and evolution · 2019
    Article
  16. Article
  17. Article
  18. Double abdomen in a short-germ insect: Zygotic control of axis formation revealed in the beetleProceedings of the National Academy of Sciences of the United States of America · 2018
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  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.

Georg OberhoferDepartment of Evolutionary Developmental Biology, Johann Friedrich Blumenbach Institute of Zoology and Anthropology, Georg-August-University, Justus von Liebig Weg 11, Göttingen D-37077, Germany.
Daniela GrossmannDepartment of Evolutionary Developmental Biology, Johann Friedrich Blumenbach Institute of Zoology and Anthropology, Georg-August-University, Justus von Liebig Weg 11, Göttingen D-37077, Germany.
Janna L SiemanowskiDepartment of Evolutionary Developmental Biology, Johann Friedrich Blumenbach Institute of Zoology and Anthropology, Georg-August-University, Justus von Liebig Weg 11, Göttingen D-37077, Germany.
Tim BeissbarthDepartment of Medical Statistics, University Medical Center Göttingen, Humboldtallee 32, Göttingen D-37073, Germany.
Gregor BucherDepartment of Evolutionary Developmental Biology, Johann Friedrich Blumenbach Institute of Zoology and Anthropology, Georg-August-University, Justus von Liebig Weg 11, Göttingen D-37077, Germany gbucher1@uni-goettingen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt/β-catenin and hedgehog (Hh) signaling are essential for transmitting signals across cell membranes in animal embryos. Early patterning of the principal insect model, Drosophila melanogaster, occurs in the syncytial blastoderm, where diffusion of transcription factors obviates the need for signaling pathways. However, in the cellularized growth zone of typical short germ insect embryos, signaling pathways are predicted to play a more fundamental role. Indeed, the Wnt/β-catenin pathway is required for posterior elongation in most arthropods, although which target genes are activated in this context remains elusive. Here, we use the short germ beetle Tribolium castaneum to investigate two Wnt and Hh signaling centers located in the head anlagen and in the growth zone of early embryos. We find that Wnt/β-catenin signaling acts upstream of Hh in the growth zone, whereas the opposite interaction occurs in the head. We determine the target gene sets of the Wnt/β-catenin and Hh pathways and find that the growth zone signaling center activates a much greater number of genes and that the Wnt and Hh target gene sets are essentially non-overlapping. The Wnt pathway activates key genes of all three germ layers, including pair-rule genes, and Tc-caudal and Tc-twist. Furthermore, the Wnt pathway is required for hindgut development and we identify Tc-senseless as a novel hindgut patterning gene required in the early growth zone. At the same time, Wnt acts on growth zone metabolism and cell division, thereby integrating growth with patterning. Posterior Hh signaling activates several genes potentially involved in a proteinase cascade of unknown function.

Indexed as

AnimalsBase Sequencebeta CateninBody PatterningDrosophila ProteinsEnergy MetabolismHeadHedgehog ProteinsImage Processing, Computer-AssistedIn Situ HybridizationMicroscopy, ConfocalMolecular Sequence DataRNA InterferenceSequence Analysis, RNATranscription FactorsTriboliumbeta CateninDrosophila ProteinsHedgehog Proteinshh protein, DrosophilaTranscription FactorsGrowth zoneGutHeadHedgehogSegment addition zoneSenselessWnt

Identifiers

PMID25395458
PMCPMC4299277

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Registered trials

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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.