Evidence map›Paper›PMID 27020744›Full record

ArticleCurrent biology : CB2016

translin Is Required for Metabolic Regulation of Sleep.

Kazuma Murakami, Maria E Yurgel, Bethany A Stahl, Pavel Masek, Aradhana Mehta, Rebecca Heidker, Wesley Bollinger, Robert M Gingras, Young-Joon Kim, William W Ja and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Article
  3. Sleep regulation inFrontiers in neuroscience · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 3 countries.

Kazuma Murakami *Department of Biology, University of Nevada, Reno, NV 89557.
Maria E Yurgel *Department of Biology, University of Nevada, Reno, NV 89557.
Bethany A StahlDepartment of Biological Sciences, Florida Atlantic University, John D MacArthur Campus, Jupiter, FL, USA.
Pavel MasekDepartment of Biology, SUNY Binghamton, Binghamton, NY 13902.
Aradhana MehtaDepartment of Biology, University of Nevada, Reno, NV 89557.
Rebecca HeidkerDepartment of Biology, University of Nevada, Reno, NV 89557.
Wesley BollingerDepartment of Biology, University of Nevada, Reno, NV 89557.
Robert M GingrasDepartment of Biology, Hofstra University, Hempstead, NY, 11549.
Young-Joon KimSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, South Korea.
William W JaDepartment of Metabolism and Aging, The Scripps Research Institute, Jupiter, FL 33458.
Beat SuterUniversity of Bern, Institute of Cell Biology, Bern, Switzerland, CH-3012.
Justin R DiAngeloDepartment of Biology, Hofstra University, Hempstead, NY, 11549.
Alex C KeeneDepartment of Biology, University of Nevada, Reno, NV 89557.
University of Nevada, Reno · USBinghamton University · USFlorida Atlantic University · USGwangju Institute of Science and Technology · KRHofstra University · USPennsylvania State University · USScripps Research Institute · USUniversity of Bern · CH

Funding

The role of neural translin in metabolic control of sleepR01NS085152 · NINDS · UNIVERSITY OF NEVADA RENO · PI KEENE, ALEX C · 2014 to 2018
$1.7M
Dietary and Endocrine Regulation of SleepR15NS080155 · NINDS · UNIVERSITY OF NEVADA RENO · PI DIANGELO, JUSTIN, KEENE, ALEX C · 2013 to 2013
$368k
NINDS NIH HHS 1R01 NS085252NINDS NIH HHS R01 NS085152NINDS NIH HHS R15 NS080155NINDS NIH HHS R15NS080155
6 · The paper itself

Abstract

Dysregulation of sleep or feeding has enormous health consequences. In humans, acute sleep loss is associated with increased appetite and insulin insensitivity, while chronically sleep-deprived individuals are more likely to develop obesity, metabolic syndrome, type II diabetes, and cardiovascular disease. Conversely, metabolic state potently modulates sleep and circadian behavior; yet, the molecular basis for sleep-metabolism interactions remains poorly understood. Here, we describe the identification of translin (trsn), a highly conserved RNA/DNA binding protein, as essential for starvation-induced sleep suppression. Strikingly, trsn does not appear to regulate energy stores, free glucose levels, or feeding behavior suggesting the sleep phenotype of trsn mutant flies is not a consequence of general metabolic dysfunction or blunted response to starvation. While broadly expressed in all neurons, trsn is transcriptionally upregulated in the heads of flies in response to starvation. Spatially restricted rescue or targeted knockdown localizes trsn function to neurons that produce the tachykinin family neuropeptide Leucokinin. Manipulation of neural activity in Leucokinin neurons revealed these neurons to be required for starvation-induced sleep suppression. Taken together, these findings establish trsn as an essential integrator of sleep and metabolic state, with implications for understanding the neural mechanism underlying sleep disruption in response to environmental perturbation.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsFeeding BehaviorHumansModels, AnimalSleepStarvationDrosophila Proteinstrsn protein, Drosophila

Identifiers

PMID27020744
PMCPMC4846466
OpenAlexW2303447128

What OpenQuestion holds

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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.