Evidence map›Paper›PMID 24223770›Full record

ArticlePloS one2013

UNC79 and UNC80, putative auxiliary subunits of the NARROW ABDOMEN ion channel, are indispensable for robust circadian locomotor rhythms in Drosophila.

Bridget C Lear, Eric J Darrah, Benjamin T Aldrich, Senetibeb Gebre, Robert L Scott, Howard A Nash, Ravi Allada

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  11. The E3 ubiquitin ligase adaptorProceedings of the National Academy of Sciences of the United States of America · 2021
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  18. Progesterone and estrogen regulate NALCN expression in human myometrial smooth muscle cells.American journal of physiology. Endocrinology and metabolism · 2020
    Article
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  20. Forward genetic approach for behavioral neuroscience using animal models.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2020
    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 3 institutions in 1 country.

Bridget C LearDepartment of Biology, University of Iowa, Iowa City, Iowa, United States of America.
Eric J Darrah
Benjamin T Aldrich
Senetibeb Gebre
Robert L Scott
Howard A Nash
Ravi Allada
University of Iowa · USNational Institute of Mental Health · USNorthwestern University · US

Funding

Function of the Novel Ion Channel narrow abdomen in Daily RhythmsR01NS052903 · NINDS · NORTHWESTERN UNIVERSITY · PI ALLADA, RAVI · 2005 to 2008
$1.3M
Regulation of a Pacemaker Neural Output in Drosophila Circadian RhythmsR00GM080107 · NIGMS · UNIVERSITY OF IOWA · PI LEAR, BRIDGET C · 2010 to 2012
$742k
NIGMS NIH HHS R00 GM080107NINDS NIH HHS R01 NS052903
6 · The paper itself

Abstract

In the fruit fly Drosophila melanogaster, a network of circadian pacemaker neurons drives daily rhythms in rest and activity. The ion channel NARROW ABDOMEN (NA), orthologous to the mammalian sodium leak channel NALCN, functions downstream of the molecular circadian clock in pacemaker neurons to promote behavioral rhythmicity. To better understand the function and regulation of the NA channel, we have characterized two putative auxiliary channel subunits in Drosophila, unc79 (aka dunc79) and unc80 (aka CG18437). We have generated novel unc79 and unc80 mutations that represent strong or complete loss-of-function alleles. These mutants display severe defects in circadian locomotor rhythmicity that are indistinguishable from na mutant phenotypes. Tissue-specific RNA interference and rescue analyses indicate that UNC79 and UNC80 likely function within pacemaker neurons, with similar anatomical requirements to NA. We observe an interdependent, post-transcriptional regulatory relationship among the three gene products, as loss of na, unc79, or unc80 gene function leads to decreased expression of all three proteins, with minimal effect on transcript levels. Yet despite this relationship, we find that the requirement for unc79 and unc80 in circadian rhythmicity cannot be bypassed by increasing NA protein expression, nor can these putative auxiliary subunits substitute for each other. These data indicate functional requirements for UNC79 and UNC80 beyond promoting channel subunit expression. Immunoprecipitation experiments also confirm that UNC79 and UNC80 form a complex with NA in the Drosophila brain. Taken together, these data suggest that Drosophila NA, UNC79, and UNC80 function together in circadian clock neurons to promote rhythmic behavior.

Indexed as

AllelesAnimalsBrainCircadian ClocksCircadian RhythmDrosophilaDrosophila ProteinsFemaleGene Expression RegulationIon ChannelsLocomotionMaleMembrane ProteinsMitochondrial Membrane Transport ProteinsMutationNeuronsDrosophila ProteinsGC1 protein, DrosophilaIon ChannelsMembrane ProteinsMitochondrial Membrane Transport ProteinsNa protein, Drosophilaunc79 protein, Drosophila

Identifiers

PMID24223770
PMCPMC3818319
OpenAlexW2048352825

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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.