Evidence map›Paper›PMID 31593608›Full record

ArticleAlcoholism, clinical and experimental research2019

F654A and K558Q Mutations in NMDA Receptor 1 Affect Ethanol-Induced Behaviors in Drosophila.

Benjamin Troutwine, Annie Park, Maria E Velez-Hernandez, Linda Lew, S John Mihic, Nigel S Atkinson

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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  9. Flying Together:International journal of molecular sciences · 2020
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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

6 authors at 2 institutions in 1 country.

Benjamin TroutwineDepartment of Neuroscience and Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas.
Annie ParkDepartment of Neuroscience and Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas.
Maria E Velez-HernandezBiological and Health Sciences Department at Texas A&M University-Kingsville, Kingsville, Texas.
Linda LewDepartment of Neuroscience and Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas.
S John MihicDepartment of Neuroscience and Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas.
Nigel S AtkinsonDepartment of Neuroscience and Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, Texas.ORCID 0000-0001-8963-7478
The University of Texas at Austin · USTexas A&M University – Kingsville · US

Funding

Epigenetic modification as a mechanism to produce functional toleranceR01AA018037 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI ATKINSON, NIGEL S · 2008 to 2018
$3.3M
The role of Drosophila CrebA in ethanol toleranceF31AA021326 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI TROUTWINE, BENJAMIN R. · 2012 to 2015
$115k
NIAAA NIH HHS F31 AA021326NIAAA NIH HHS R01 AA018037
6 · The paper itself

Abstract

backgroundN-methyl-D-aspartate (NMDA) receptors regulate synaptic plasticity and modulate a wide variety of behaviors. Mammalian NMDA receptors are inhibited by ethanol (EtOH) even at low concentrations. In mice, the F639A mutation in transmembrane domain (TMD) 3 of the NR1 subunit reduces EtOH sensitivity of the receptor and, in some paradigms, reduces behavioral EtOH sensitivity and increases EtOH consumption. We tested the fly equivalent of the F639A and K544Q mutations for effects on EtOH sensitivity. Drosophila shows a high degree of behavioral and mechanistic conservation in its responses to EtOH.

methodsHomologous recombination and CRISPR/Cas9 genome editing were used to generate amino acid changes in the Drosophila NMDAR1 gene, yielding F654A and K558Q alleles. Animals were tested for the degree of EtOH sensitivity, the ability to acquire tolerance to EtOH, EtOH drinking preference, circadian rhythmicity, learning, and locomotor defects.

resultsWe observed that mutating the NMDAR1 channel also reduces EtOH sensitivity in adult flies. However, in flies, it was the K558Q mutation (orthologous to K544Q in mice) that reduces EtOH sensitivity in a recovery-from-sedation assay. The effects of the F654A mutation (orthologous to F639A in mice) were substantially different in flies than in mammals. In flies, F654A mutation produces phenotypes opposite those in mammals. In flies, the mutant allele is homozygous viable, does not seem to affect health, and increases EtOH sensitivity. Both mutations increased feeding but did not alter the animal's preference for 5% EtOH food. F654A depressed circadian rhythmicity and the capacity of males to court, but it did not depress the capacity for associative learning. K554Q, on the other hand, has little effect on circadian rhythmicity, only slightly suppresses male courtship, and is a strong learning mutant.

conclusionsMutations in TMD 3 and in the extracellular-vestibule calcium-binding site of the NR1 NMDA subunit affect EtOH sensitivity in Drosophila.

Indexed as

Alcohol DrinkingAllelesAnimalsBehavior, AnimalChoice BehaviorCircadian RhythmDrosophila melanogasterDrug ToleranceEatingEthanolLearningMotor ActivityMutationPhenotypeReceptors, N-Methyl-D-AspartateEthanolReceptors, N-Methyl-D-AspartateAlcoholAlcoholismCircadian RhythmsDrosophilaEtOHEtOH PreferenceLearning and MemoryNMDA ReceptorTolerance

Identifiers

PMID31593608
PMCPMC9210938
OpenAlexW2980061547

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.