Evidence map›Paper›PMID 19101836›Full record

ArticleJournal of neurogenetics2009

Role of rut adenylyl cyclase in the ensemble regulation of presynaptic terminal excitability: reduced synaptic strength and precision in a Drosophila memory mutant.

Atsushi Ueda, Chun-Fang Wu

Open access · greenAbstract read
In one paragraph

Article in Journal of neurogenetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Rapid active zone remodeling during synaptic plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  10. Behavioral and synaptic plasticity are impaired upon lack of the synaptic protein SAP47.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  11. Article
  12. Article
  13. Article
  14. 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

2 authors at 1 institution in 1 country.

Atsushi UedaDepartment of Biological Sciences, University of Iowa, Iowa City, Iowa 52242, USA.
Chun-Fang Wu
University of Iowa · US

Funding

VIDEO LABORATORY FOR ANALYSIS OF CELL BEHAVIORP01HD018577 · NICHD · UNIVERSITY OF IOWA · PI VOSS, EDWARD R · 1985 to 2006
$5.1M
Plasticity of Neuronal Function and Form in DrosophilaR01NS026528 · NINDS · UNIVERSITY OF IOWA · PI WU, CHUN-FANG · 1988 to 2007
$2.0M
NICHD NIH HHS HD18577NICHD NIH HHS P01 HD018577NINDS NIH HHS NS26528NINDS NIH HHS R01 NS026528
6 · The paper itself

Abstract

Although modulation of presynaptic terminal excitability can profoundly affect transmission efficacy, how excitability along axonal terminal branches is regulated requires further investigations. We performed focal patch recording in Drosophila larval neuromuscular junctions (NMJs) to monitor the activity of individual synaptic boutons along the presynaptic terminal. Analysis of the learning mutant rutabaga (rut) suggests a tight regulation of presynaptic terminal excitability by rut adenylyl cyclase (AC) that is responsible for Ca2+/calmodulin-dependent cAMP synthesis. Focal excitatory junctional currents (ejcs) demonstrated that disrupted cAMP metabolism in rut mutant boutons leads to decreased transmitter release, coupled with temporal dispersion and amplitude fluctuation of ejcs during repetitive activity. Strikingly, rut motor terminals displayed greatly increased variability among corresponding terminal branches of identified NMJs in different preparations. However, boutons throughout single terminal branches were relatively uniform in either WT or rut mutant larvae. The use of electrotonic depolarization to directly evoke transmitter release from axonal terminals revealed that variability in neurotransmission originated from varying degrees of weakened excitability in rut terminals. Pharmacological treatments and axonal action potential recordings raised the possibility that defective rut AC resulted in reduced Ca2+ currents in the nerve terminal. Thus, our data indicate that rut AC not only affects transmitter release machinery, but also plays a previously unsuspected role in local excitability control, both contributing to transmission level and precision along the entire axonal terminal.

Indexed as

Action PotentialsAdenylyl CyclasesAnimalsCalciumCalcium ChannelsCyclic AMPDrosophila melanogasterDrosophila ProteinsMemoryMutationNeuromuscular JunctionNeuronal PlasticityPatch-Clamp TechniquesPresynaptic TerminalsSodiumSynaptic TransmissionAdenylyl CyclasesCalciumCalcium ChannelsCyclic AMPDrosophila ProteinsRut protein, DrosophilaSodium

Identifiers

PMID19101836
PMCPMC2743603
OpenAlexW1989999666

What OpenQuestion holds

Textmetadata
LicenceTDM
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.