Evidence map›Paper›PMID 23097047›Full record

ArticleJournal of cell science2012

The conserved P body component HPat/Pat1 negatively regulates synaptic terminal growth at the larval Drosophila neuromuscular junction.

Sarala J Pradhan, Katherine R Nesler, Sarah F Rosen, Yasuko Kato, Akira Nakamura, Mani Ramaswami, Scott A Barbee

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  6. Vps54 regulatesBiology open · 2020
    Article
  7. The Role of Dynamic miRISC During Neuronal Development.Frontiers in molecular biosciences · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Genetic mapping of male pheromone response in the European corn borer identifies candidate genes regulating neurogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  12. Article
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  15. Review
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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

7 authors at 4 institutions in 3 countries.

Sarala J PradhanDepartment of Biological Sciences and Eleanor Roosevelt Institute, University of Denver, Denver, CO 80208, USA.
Katherine R Nesler
Sarah F Rosen
Yasuko Kato
Akira Nakamura
Mani Ramaswami
Scott A Barbee
RIKEN Center for Biosystems Dynamics Research · JPRoosevelt Institute · USUniversity of Denver · USTrinity College Dublin · IE

Funding

P-Body and miRNA-Mediated Regulation of NeuroplasticityR01DA026048 · NIDA · UNIVERSITY OF DENVER (COLORADO SEMINARY) · PI BARBEE, SCOTT A · 2008 to 2011
$1.2M
NIDA NIH HHS R01 DA026048NIDA NIH HHS R01DA26048
6 · The paper itself

Abstract

The temporal and spatial regulation of protein synthesis plays an important role in the control of neural physiology. In axons and dendrites, translationally repressed mRNAs are actively transported to their destinations in a variety of ribonucleoprotein particles (RNPs). A subset of these neuronal RNPs has been shown to contain proteins associated with mRNA processing bodies (P bodies). P bodies are a class of highly conserved cytoplasmic granules that have been linked to both mRNA decay and translational repression via general and miRNA-mediated pathways. Here, we characterize functions for HPat/Pat1 (also known as Patr-1), a core component of P bodies, at the glutamatergic larval Drosophila neuromuscular junction (NMJ). We show that hpat mutants exhibit a strong synaptic hyperplasia at the NMJ. The synaptic defects observed in hpat mutants are associated with rearrangement of the axonal microtubule cytoskeleton suggesting that HPat negatively regulates presynaptic microtubule-based growth during NMJ development. Consistent with this, overexpression of HPat also blocks the rapid growth of presynaptic boutons induced by spaced depolarization. Finally, we demonstrate that HPat interacts genetically with the catalytic subunit of the deadenylase complex (twin/CCR4) and the miRNA pathway (Argonaute 1) to control bouton formation. We propose that HPat is required to target mRNAs involved in the control of microtubule architecture and synaptic terminal growth for repression, presumably in P bodies, via both general and miRNA-mediated mechanisms.

Indexed as

AnimalsCarrier ProteinsCytoskeletonDrosophilaDrosophila ProteinsFemaleMaleNeuromuscular JunctionPresynaptic TerminalsRNA-Binding ProteinsSynaptic TransmissionCarrier ProteinsDrosophila ProteinsPAT1 protein, DrosophilaPatr-1 protein, DrosophilaRNA-Binding Proteins

Identifiers

PMID23097047
PMCPMC3585522
OpenAlexW2104921072

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.