Evidence map›Paper›PMID 23048183›Full record

ArticleDevelopment (Cambridge, England)2012

Torso RTK controls Capicua degradation by changing its subcellular localization.

Oliver Grimm, Victoria Sanchez Zini, Yoosik Kim, Jordi Casanova, Stanislav Y Shvartsman, Eric Wieschaus

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Noncanonical function of Capicua as a growth termination signal inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Dynamics ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Antagonism betweeneLife · 2021
    Article
  17. Capicua in Human Cancer.Trends in cancer · 2021
    Review
  18. Optogenetic Rescue of a Patterning Mutant.Current biology : CB · 2020
    Article
  19. Negative MAPK-ERK regulation sustains CIC-DUX4 oncoprotein expression in undifferentiated sarcoma.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

6 authors at 3 institutions in 2 countries.

Oliver GrimmHoward Hughes Medical Institute, Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Victoria Sanchez Zini
Yoosik Kim
Jordi Casanova
Stanislav Y Shvartsman
Eric Wieschaus
Princeton University · USHoward Hughes Medical Institute · USInstitut de Biologia Molecular de Barcelona · ES

Funding

Spatial Patterning During DevelopmentP50GM071508 · NIGMS · PRINCETON UNIVERSITY · PI POWELL, SUSAN M · 2004 to 2013
$30.6M
Systems biology of MAPK signaling in early drosophila embryoR01GM086537 · NIGMS · PRINCETON UNIVERSITY · PI BURDINE, REBECCA D., GOLDSMITH, ELIZABETH J. · 2011 to 2018
$3.1M
Dynamics, scaling, and precision of morphogen gradients in the Drosophila embryoR01GM077599 · NIGMS · PRINCETON UNIVERSITY · PI BIALEK, WILLIAM · 2006 to 2009
$1.2M
Howard Hughes Medical InstituteNIGMS NIH HHS P50 GM071508NIGMS NIH HHS P50-GM-071508NIGMS NIH HHS R01 GM077599NIGMS NIH HHS R01-GM077599NIGMS NIH HHS R01 GM086537NIGMS NIH HHS R01GM086537
6 · The paper itself

Abstract

The transcriptional repressor Capicua (Cic) controls multiple aspects of Drosophila embryogenesis and has been implicated in vertebrate development and human diseases. Receptor tyrosine kinases (RTKs) can antagonize Cic-dependent gene repression, but the mechanisms responsible for this effect are not fully understood. Based on genetic and imaging studies in the early Drosophila embryo, we found that Torso RTK signaling can increase the rate of Cic degradation by changing its subcellular localization. We propose that Cic is degraded predominantly in the cytoplasm and show that Torso reduces the stability of Cic by controlling the rates of its nucleocytoplasmic transport. This model accounts for the experimentally observed spatiotemporal dynamics of Cic in the early embryo and might explain RTK-dependent control of Cic in other developmental contexts.

Indexed as

AnimalsBlotting, WesternBody PatterningDrosophilaDrosophila ProteinsFemaleFluorescence Recovery After PhotobleachingGene Expression Regulation, DevelopmentalHMGB ProteinsMaleReceptor Protein-Tyrosine KinasesRepressor ProteinsReverse Transcriptase Polymerase Chain ReactionSignal Transductioncic protein, DrosophilaDrosophila ProteinsHMGB ProteinsReceptor Protein-Tyrosine KinasesRepressor Proteinstor protein, Drosophila

Identifiers

PMID23048183
PMCPMC3472588
OpenAlexW2161118640

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.