Evidence map›Paper›PMID 16407556›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

Functional dissection of a neuronal network required for cuticle tanning and wing expansion in Drosophila.

Haojiang Luan, William C Lemon, Nathan C Peabody, Jascha B Pohl, Paul K Zelensky, Ding Wang, Michael N Nitabach, Todd C Holmes, Benjamin H White

Abstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing 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

109 citing papers in PubMed.

  1. Article
  2. Review
  3. Gene Expression ofInternational journal of molecular sciences · 2026
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  13. A novel post-developmental role of the Hox genes underlies normal adult behavior.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  20. Parallel Synaptic Acetylcholine Signals Facilitate Large Monopolar Cell Repolarization and Modulate Visual Behavior inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article

49 more citing papers are in PubMed but not listed here.

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

9 authors.

Haojiang LuanLaboratory of Molecular Biology, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892, USA.
William C Lemon
Nathan C Peabody
Jascha B Pohl
Paul K Zelensky
Ding Wang
Michael N Nitabach
Todd C Holmes
Benjamin H White

Funding

Identifying Neural Substrates of Behavior in Drosophila MelanogasterZ01MH002800 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI WHITE, BENJAMIN H · 2003 to 2008
$2.7M
Electrical Signaling in a Circadian Pacemaker CircuitR01NS046750 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HOLMES, TODD C · 2004 to 2013
$2.4M
Intramural NIH HHSNIMH NIH HHS Z01 MH002800-03NINDS NIH HHS R01 NS046750NINDS NIH HHS R01-NS046750
6 · The paper itself

Abstract

A subset of Drosophila neurons that expresses crustacean cardioactive peptide (CCAP) has been shown previously to make the hormone bursicon, which is required for cuticle tanning and wing expansion after eclosion. Here we present evidence that CCAP-expressing neurons (NCCAP) consist of two functionally distinct groups, one of which releases bursicon into the hemolymph and the other of which regulates its release. The first group, which we call NCCAP-c929, includes 14 bursicon-expressing neurons of the abdominal ganglion that lie within the expression pattern of the enhancer-trap line c929-Gal4. We show that suppression of activity within this group blocks bursicon release into the hemolymph together with tanning and wing expansion. The second group, which we call NCCAP-R, consists of NCCAP neurons outside the c929-Gal4 pattern. Because suppression of synaptic transmission and protein kinase A (PKA) activity throughout NCCAP, but not in NCCAP-c929, also blocks tanning and wing expansion, we conclude that neurotransmission and PKA are required in NCCAP-R to regulate bursicon secretion from NCCAP-c929. Enhancement of electrical activity in NCCAP-R by expression of the bacterial sodium channel NaChBac also blocks tanning and wing expansion and leads to depletion of bursicon from central processes. NaChBac expression in NCCAP-c929 is without effect, suggesting that the abdominal bursicon-secreting neurons are likely to be silent until stimulated to release the hormone. Our results suggest that NCCAP form an interacting neuronal network responsible for the regulation and release of bursicon and suggest a model in which PKA-mediated stimulation of inputs to normally quiescent bursicon-expressing neurons activates release of the hormone.

Indexed as

AnimalsAnimals, Genetically ModifiedBacterial ProteinsCyclic AMP-Dependent Protein KinasesDrosophila melanogasterDrosophila ProteinsElectroretinographyGanglia, InvertebrateGene TargetingInvertebrate HormonesNerve NetNeuronsNeuropeptidesPhenotypePigmentationRecombinant Fusion ProteinsBacterial Proteinsbursiconcrustacean cardioactive peptideCyclic AMP-Dependent Protein KinasesDrosophila ProteinsInvertebrate HormonesNaChBac protein, bacteriaNeuropeptidesRecombinant Fusion ProteinsShaker Superfamily of Potassium ChannelsSh protein, DrosophilaSodium Channels

Identifiers

PMID16407556
PMCPMC1857274

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.