Evidence map›Paper›PMID 28902472›Full record

ArticleGenes, brain, and behavior2018

The mushroom body D1 dopamine receptor controls innate courtship drive.

J Lim, A I Fernandez, S J Hinojos, G P Aranda, J James, C-S Seong, K-A Han

Open access · hybridAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2018. 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
1.8field-weighted citation impact, top 16% 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, 42 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Review
  9. The making of the Drosophila mushroom body.Frontiers in physiology · 2023
    Review
  10. Article
  11. Article
  12. Semaphorin 1a-mediated dendritic wiring of theProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Biology open · 2018
    Article
  17. Review
  18. 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 1 institution in 1 country.

J LimNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
A I FernandezNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
S J HinojosNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
G P ArandaNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
J JamesNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
C-S SeongNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
K-A HanNeuromodulation Disorders Cluster at Border Biomedical Research Center, Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.ORCID 0000-0001-7972-1764
The University of Texas at El Paso · US

Funding

TCCG12MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI KIRKEN, ROBERT A. · 2012 to 2018
$19.4M
RISE Scholars Program at UTEPR25GM069621 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI AGUILERA, RENATO J · 2004 to 2021
$11.2M
Research Supplement to Promote Diversity in Health-Related ResearchR15AA020996 · NIAAA · UNIVERSITY OF TEXAS EL PASO · PI HAN, KYUNG-AN · 2012 to 2014
$499k
NIAAA NIH HHS R15 AA020996NIGMS NIH HHS R25 GM069621NIMHD NIH HHS G12 MD007592
6 · The paper itself

Abstract

Mating is critical for species survival and is profoundly regulated by neuromodulators and neurohormones to accommodate internal states and external factors. To identify the underlying neuromodulatory mechanisms, we investigated the roles of dopamine receptors in various aspects of courtship behavior in Drosophila. Here, we report that the D1 dopamine receptor dDA1 regulates courtship drive in naïve males. The wild-type naïve males actively courted females regardless their appearance or mating status. On the contrary, the dDA1 mutant (dumb) males exhibited substantially reduced courtship toward less appealing females including decapitated, leg-less and mated females. The dumb male's reduced courtship activity was due to delay in courtship initiation and prolonged intervals between courtship bouts. The dampened courtship drive of dumb males was rescued by reinstated dDA1 expression in the mushroom body α/β and γ neurons but not α/β or γ neurons alone, which is distinct from the previously characterized dDA1 functions in experience-dependent courtship or other learning and memory processes. We also found that the dopamine receptors dDA1, DAMB and dD2R are dispensable for associative memory formation and short-term memory of conditioned courtship, thus courtship motivation and associative courtship learning and memory are regulated by distinct neuromodulatory mechanisms. Taken together, our study narrows the gap in the knowledge of the mechanism that dopamine regulates male courtship behavior.

Indexed as

AnimalsBehavior, AnimalConditioning, ClassicalCourtshipDopamineDopaminergic NeuronsDrosophilaDrosophila ProteinsMemoryMushroom BodiesReceptors, DopamineDopamineDrosophila ProteinsReceptors, DopamineConditioningcourtshipD1 receptordopamineDrosophilalearningmating decisionmemorymotivationmushroom body

Identifiers

PMID28902472
PMCPMC5820115
OpenAlexW2755240840

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.