Evidence map›Paper›PMID 20554864›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

dCIP4 (Drosophila Cdc42-interacting protein 4) restrains synaptic growth by inhibiting the secretion of the retrograde Glass bottom boat signal.

Minyeop Nahm, Sungdae Kim, Sang Kyoo Paik, Mihye Lee, Seongsoo Lee, Zang Hee Lee, Jaesang Kim, Daekee Lee, Yong Chul Bae, Seungbok Lee

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Targeted Downregulation ofJournal of Korean medical science · 2019
    Article
  7. Article
  8. Genetics · 2018
    Article
  9. Article
  10. TGF-β Family Signaling inCold Spring Harbor perspectives in biology · 2017
    Review
  11. Article
  12. Pathogenic Huntington Alters BMP Signaling and Synaptic Growth through Local Disruptions of Endosomal Compartments.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  13. Article
  14. Article
  15. Coordinated autoinhibition of F-BAR domain membrane binding and WASp activation by Nervous Wreck.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  16. Review
  17. 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

10 authors.

Minyeop NahmInterdisciplinary Graduate Program in Brain Science, Department of Cell and Developmental Biology, Dental Research Institute, Seoul National University, Seoul 110-740, Republic of Korea.
Sungdae Kim
Sang Kyoo Paik
Mihye Lee
Seongsoo Lee
Zang Hee Lee
Jaesang Kim
Daekee Lee
Yong Chul Bae
Seungbok Lee

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bone morphogenetic protein (BMP) ligand Glass bottom boat (Gbb) acts as a retrograde growth signal at the Drosophila neuromuscular junction (NMJ). Endocytic regulation of presynaptic BMP receptors has been proposed to attenuate retrograde BMP signaling. However, it remains unknown whether the Gbb signal is also regulated by postsynaptic mechanisms. Here, we provide evidence that Drosophila Cdc42-interacting protein 4 (dCIP4) functions postsynaptically to inhibit synaptic growth. dCIP4 is localized postsynaptically at NMJs. dcip4 mutations lead to synaptic overgrowth and increased presynaptic phosphorylated mothers against decapentaplegic (Mad) levels, and these defects are rescued by muscle-specific expression of dCIP4. Biochemical and genetic analyses demonstrate that dCIP4 acts downstream of Cdc42 to activate the postsynaptic Wsp-Arp2/3 pathway. We also show that BMP signaling is necessary for synaptic overgrowth in larvae lacking postsynaptic dcip4 or wsp. Finally, dCIP4 and Wsp inhibit Gbb secretion. Thus, we propose that dCIP4 restrains synaptic growth by inhibiting postsynaptic Gbb secretion through the Wsp-Arp2/3 pathway.

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedBone Morphogenetic ProteinsCarrier ProteinsCells, CulturedDrosophilaDrosophila ProteinsGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHumansMicroscopy, ConfocalMolecular BiologyMutationNerve Tissue ProteinsNeuromuscular JunctionBone Morphogenetic ProteinsCarrier ProteinsCip4 protein, Drosophiladpp protein, DrosophilaDrosophila Proteinsgbb protein, DrosophilaGreen Fluorescent ProteinsNerve Tissue ProteinsTransforming Growth Factor beta

Identifiers

PMID20554864
PMCPMC6634589

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.