Evidence map›Paper›PMID 22391052›Full record

ArticleDevelopmental biology2012

Combinatorial use of translational co-factors for cell type-specific regulation during neuronal morphogenesis in Drosophila.

Eugenia C Olesnicky, Balpreet Bhogal, Elizabeth R Gavis

Abstract read
In one paragraph

Article in Developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Role of Dynamic miRISC During Neuronal Development.Frontiers in molecular biosciences · 2020
    Review
  6. Article
  7. Article
  8. Journal of developmental biology · 2018
    Review
  9. Article
  10. Shep regulatesDevelopment (Cambridge, England) · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The TRIM-NHL protein Brat promotes axon maintenance by repressing src64B expression.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  17. Article
  18. Review
  19. 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

3 authors at 1 institution in 1 country.

Eugenia C OlesnickyDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Balpreet Bhogal
Elizabeth R Gavis
Princeton University · US

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Translational Regulation of Patterning in DrosphilaR01GM061107 · NIGMS · PRINCETON UNIVERSITY · PI GAVIS, ELIZABETH R · 2001 to 2017
$5.2M
The regulation of neural crest cell migration during zebrafish developmentF32HD056779 · NICHD · UNIVERSITY OF COLORADO DENVER · PI OLESNICKY, EUGENIA C · 2008 to 2010
$149k
NICHD NIH HHS F32 HD056779NIGMS NIH HHS R01 GM061107NIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947
6 · The paper itself

Abstract

The translational regulators Nanos (Nos) and Pumilio (Pum) work together to regulate the morphogenesis of dendritic arborization (da) neurons of the Drosophila larval peripheral nervous system. In contrast, Nos and Pum function in opposition to one another in the neuromuscular junction to regulate the morphogenesis and the electrophysiological properties of synaptic boutons. Neither the cellular functions of Nos and Pum nor their regulatory targets in neuronal morphogenesis are known. Here we show that Nos and Pum are required to maintain the dendritic complexity of da neurons during larval growth by promoting the outgrowth of new dendritic branches and the stabilization of existing dendritic branches, in part by regulating the expression of cut and head involution defective. Through an RNA interference screen we uncover a role for the translational co-factor Brain Tumor (Brat) in dendrite morphogenesis of da neurons and demonstrate that Nos, Pum, and Brat interact genetically to regulate dendrite morphogenesis. In the neuromuscular junction, Brat function is most likely specific for Pum in the presynaptic regulation of bouton morphogenesis. Our results reveal how the combinatorial use of co-regulators like Nos, Pum and Brat can diversify their roles in post-transcriptional regulation of gene expression for neuronal morphogenesis.

Indexed as

AnimalsCell DifferentiationDNA-Binding ProteinsDrosophilaDrosophila ProteinsGene Expression Regulation, DevelopmentalLarvaMorphogenesisNeuronsRNA-Binding ProteinsRNA Processing, Post-Transcriptionalbrat protein, DrosophilaDNA-Binding ProteinsDrosophila Proteinsnos protein, Drosophilapum protein, DrosophilaRNA-Binding Proteins

Identifiers

PMID22391052
PMCPMC3642870
OpenAlexW2132035030

What OpenQuestion holds

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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.