Evidence map›Paper›PMID 25099506›Full record

ArticlePloS one2014

The octopamine receptor Octβ2R regulates ovulation in Drosophila melanogaster.

Junghwa Lim, Paul R Sabandal, Ana Fernandez, John Martin Sabandal, Hyun-Gwan Lee, Peter Evans, Kyung-An Han

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

51 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Octopamine receptors inFrontiers in molecular neuroscience · 2026
    Article
  6. Molecular evolution of octopamine receptors inbioRxiv : the preprint server for biology · 2025
    Article
  7. Female membrane proteins regulate postmating ovulation inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Octopamine in the mushroom body circuitry for learning and memory.Learning & memory (Cold Spring Harbor, N.Y.) · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Finishing the egg.Genetics · 2024
    Article
  15. Article
  16. Article
  17. Identification of CYCLE targets that contribute diverse features of circadian rhythms in the mosquito Culex pipiens.Comparative biochemistry and physiology. Part D, Genomics & proteomics · 2023
    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

7 authors at 2 institutions in 2 countries.

Junghwa LimDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
Paul R SabandalDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
Ana FernandezDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
John Martin SabandalDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
Hyun-Gwan LeeDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
Peter EvansThe Inositide Laboratory, The Babraham Institute, Cambridge, United Kingdom.
Kyung-An HanDepartment of Biological Sciences, Border Biomedical Research Center/Neuroscience and Metabolic Disorders, University of Texas at El Paso, El Paso, Texas, United States of America.
The University of Texas at El Paso · USBabraham Institute · GB

Funding

TCCG12MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI KIRKEN, ROBERT A. · 2012 to 2018
$19.4M
Biotechnology and Biological Sciences Research Council BBS/E/B/00001194Biotechnology and Biological Sciences Research Council BBS/E/B/0000C194NIMHD NIH HHS 8G12MD007592NIMHD NIH HHS G12 MD007592
6 · The paper itself

Abstract

Oviposition is induced upon mating in most insects. Ovulation is a primary step in oviposition, representing an important target to control insect pests and vectors, but limited information is available on the underlying mechanism. Here we report that the beta adrenergic-like octopamine receptor Octβ2R serves as a key signaling molecule for ovulation and recruits protein kinase A and Ca(2+)/calmodulin-sensitive kinase II as downstream effectors for this activity. We found that the octβ2r homozygous mutant females are sterile. They displayed normal courtship, copulation, sperm storage and post-mating rejection behavior but were unable to lay eggs. We have previously shown that octopamine neurons in the abdominal ganglion innervate the oviduct epithelium. Consistently, restored expression of Octβ2R in oviduct epithelial cells was sufficient to reinstate ovulation and full fecundity in the octβ2r mutant females, demonstrating that the oviduct epithelium is a major site of Octβ2R's function in oviposition. We also found that overexpression of the protein kinase A catalytic subunit or Ca(2+)/calmodulin-sensitive protein kinase II led to partial rescue of octβ2r's sterility. This suggests that Octβ2R activates cAMP as well as additional effectors including Ca(2+)/calmodulin-sensitive protein kinase II for oviposition. All three known beta adrenergic-like octopamine receptors stimulate cAMP production in vitro. Octβ1R, when ectopically expressed in the octβ2r's oviduct epithelium, fully reinstated ovulation and fecundity. Ectopically expressed Octβ3R, on the other hand, partly restored ovulation and fecundity while OAMB-K3 and OAMB-AS that increase Ca(2+) levels yielded partial rescue of ovulation but not fecundity deficit. These observations suggest that Octβ2R have distinct signaling capacities in vivo and activate multiple signaling pathways to induce egg laying. The findings reported here narrow the knowledge gap and offer insight into novel strategies for insect control.

Indexed as

AnimalsCyclic AMP-Dependent Protein KinasesDrosophila melanogasterDrosophila ProteinsFemaleInfertility, FemaleOviductsOvipositionReceptors, G-Protein-CoupledSignal TransductionCyclic AMP-Dependent Protein KinasesDrosophila ProteinsOctbeta2R protein, DrosophilaReceptors, G-Protein-Coupled

Identifiers

PMID25099506
PMCPMC4123956
OpenAlexW2007656488

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.