Evidence map›Paper›PMID 27601662›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Minibrain and Wings apart control organ growth and tissue patterning through down-regulation of Capicua.

Liu Yang, Sayantanee Paul, Kenneth G Trieu, Lucas G Dent, Francesca Froldi, Marta Forés, Kaitlyn Webster, Kellee R Siegfried, Shu Kondo, Kieran Harvey and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. 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
2.4field-weighted citation impact, top 11% 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, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Regulation and function of capicua in mammals.Experimental & molecular medicine · 2020
    Review
  15. Article
  16. Article
  17. Gypsy moth genome provides insights into flight capability and virus-host interactions.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. Article
  19. Review
  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

14 authors at 6 institutions in 4 countries.

Liu YangDepartment of Biology, University of Massachusetts, Boston, MA 02125;
Sayantanee PaulDepartment of Biology, University of Massachusetts, Boston, MA 02125;
Kenneth G TrieuDepartment of Biology, University of Massachusetts, Boston, MA 02125;
Lucas G DentCell Growth and Proliferation Laboratory, Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia;
Francesca FroldiCell Growth and Proliferation Laboratory, Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia;
Marta ForésInstituto de Biología Molecular de Barcelona, Consejo Superior de Investigaciones Científicas, 08028 Barcelona, Spain;
Kaitlyn WebsterDepartment of Biology, University of Massachusetts, Boston, MA 02125;
Kellee R SiegfriedDepartment of Biology, University of Massachusetts, Boston, MA 02125;
Shu KondoLaboratory of Invertebrate Genetics, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, Japan;
Kieran HarveyCell Growth and Proliferation Laboratory, Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia;
Louise ChengCell Growth and Proliferation Laboratory, Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia;
Gerardo JiménezInstituto de Biología Molecular de Barcelona, Consejo Superior de Investigaciones Científicas, 08028 Barcelona, Spain; Institució Catalana de Recerca i Estudis Avançats, 08010 Barcelona, Spain;
Stanislav Y ShvartsmanDepartment of Chemical and Biological Engineering and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544.
Alexey VeraksaDepartment of Biology, University of Massachusetts, Boston, MA 02125; alexey.veraksa@umb.edu.
University of Massachusetts Boston · USPeter MacCallum Cancer Centre · AUInstitució Catalana de Recerca i Estudis Avançats · ESInstitut de Biologia Molecular de Barcelona · ESNational Institute of Genetics · JPPrinceton University · US

Funding

Systems biology of MAPK signaling in early drosophila embryoR01GM086537 · NIGMS · PRINCETON UNIVERSITY · PI BURDINE, REBECCA D., GOLDSMITH, ELIZABETH J. · 2011 to 2018
$3.1M
Mechanisms of signal integration in developmental control of organ size and tissue patterningR01HD085870 · NICHD · UNIVERSITY OF MASSACHUSETTS BOSTON · PI VERAKSA, ALEXEY · 2016 to 2020
$1.6M
Steroid-Dependent Changes in the Yorkie InteractomeR01GM105813 · NIGMS · EMORY UNIVERSITY · PI MOBERG, KENNETH H, VERAKSA, ALEXEY · 2013 to 2016
$1.1M
NICHD NIH HHS R01 HD085870NIGMS NIH HHS R01 GM086537NIGMS NIH HHS R01 GM105813
6 · The paper itself

Abstract

The transcriptional repressor Capicua (Cic) controls tissue patterning and restricts organ growth, and has been recently implicated in several cancers. Cic has emerged as a primary sensor of signaling downstream of the receptor tyrosine kinase (RTK)/extracellular signal-regulated kinase (ERK) pathway, but how Cic activity is regulated in different cellular contexts remains poorly understood. We found that the kinase Minibrain (Mnb, ortholog of mammalian DYRK1A), acting through the adaptor protein Wings apart (Wap), physically interacts with and phosphorylates the Cic protein. Mnb and Wap inhibit Cic function by limiting its transcriptional repressor activity. Down-regulation of Cic by Mnb/Wap is necessary for promoting the growth of multiple organs, including the wings, eyes, and the brain, and for proper tissue patterning in the wing. We have thus uncovered a previously unknown mechanism of down-regulation of Cic activity by Mnb and Wap, which operates independently from the ERK-mediated control of Cic. Therefore, Cic functions as an integrator of upstream signals that are essential for tissue patterning and organ growth. Finally, because DYRK1A and CIC exhibit, respectively, prooncogenic vs. tumor suppressor activities in human oligodendroglioma, our results raise the possibility that DYRK1A may also down-regulate CIC in human cells.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBody PatterningDrosophilaDrosophila ProteinsDyrk KinasesGene Expression Regulation, DevelopmentalHMGB ProteinsHumansNeoplasmsPhosphorylationProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRepressor ProteinsWings, AnimalAdaptor Proteins, Signal Transducingcic protein, DrosophilaCIC protein, humanDrosophila ProteinsDyrk KinasesHMGB Proteinsmnb protein, DrosophilaProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRepressor ProteinscapicuaDYRK1Aminibrainorgan growthtissue patterning

Identifiers

PMID27601662
PMCPMC5035877
OpenAlexW2518353349

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.