Evidence map›Paper›PMID 32317636›Full record

ArticleNature communications2020

Circadian regulation of mitochondrial uncoupling and lifespan.

Matt Ulgherait, Anna Chen, Sophie F McAllister, Han X Kim, Rebecca Delventhal, Charlotte R Wayne, Christian J Garcia, Yocelyn Recinos, Miles Oliva, Julie C Canman and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
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

47 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. The Power of Drosophila in Modeling Cancer Cachexia.Advances in experimental medicine and biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Temperature-driven coordination of circadian transcriptome regulation.bioRxiv : the preprint server for biology · 2023
    Article
  19. Article
  20. Review
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

13 authors.

Matt UlgheraitDepartment of Genetics and Development, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Anna ChenColumbia College, New York, NY, 10027, USA.ORCID http://orcid.org/0000-0002-5946-6572
Sophie F McAllisterColumbia College, New York, NY, 10027, USA.
Han X KimDepartment of Genetics and Development, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Rebecca DelventhalDepartment of Genetics and Development, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.ORCID http://orcid.org/0000-0002-0920-0004
Charlotte R WayneDepartment of Neurology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Christian J GarciaDepartment of Physiology and Cellular Biophysics, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Yocelyn RecinosDepartment of Systems Biology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Miles OlivaColumbia College, New York, NY, 10027, USA.
Julie C CanmanDepartment of Pathology and Cell Biology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Martin PicardDepartments of Psychiatry and Neurology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Edward Owusu-AnsahDepartment of Physiology and Cellular Biophysics, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA.
Mimi Shirasu-HizaDepartment of Genetics and Development, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, 10032, USA. ms4095@cumc.columbia.edu.ORCID http://orcid.org/0000-0002-2730-1765

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI KEVIN R COOK · 2014 to 2026
$13.5M
Hormones: Molecular Mechanism of Action and FunctionsT32DK007328 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KOUSTENI, STAVROULA · 1986 to 2025
$7.8M
Circadian-Regulated Aging PhysiologiesR01AG045842 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Michele M Shirasu-Hiza · 2013 to 2026
$5.1M
Training in Cardiovascular Translational ResearchT32HL120826 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARKS, ANDREW ROBERT, TABAS, IRA A · 2014 to 2023
$4.7M
Circadian regulation of physiological functionsR35GM127049 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Michele M Shirasu-Hiza · 2018 to 2026
$3.9M
Cell type-variation of cytokinesisR01GM117407 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2016 to 2023
$2.9M
Identifying Remote Regulators of Complex I Biogenesis in DrosophilaR35GM124717 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2017 to 2021
$2.2M
Mitochondrial Stress Signal Transduction from Organelle to OrganismR35GM119793 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PICARD, MARTIN · 2016 to 2020
$1.6M
Probing the spatiotemporal regulation of cell divisionR01GM130764 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2019 to 2022
$1.3M
IGFBP-Mediated Local and Systemic Effects of Mitochondrial Dysfunction in Skeletal MusclesR21DK112074 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2016 to 2018
$594k
Genetic Dissection of OXPHOS Assembly in Skeletal MusclesR21AR077312 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2020 to 2021
$387k
Identifying Novel Regulators of Mitochondrial Complex I BiogenesisF31GM125363 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GARCIA, CHRISTIAN JOEL · 2017 to 2019
$85k
NHLBI NIH HHS T32 HL120826NIAMS NIH HHS R21 AR077312NIA NIH HHS R01 AG045842NIDDK NIH HHS R21 DK112074NIDDK NIH HHS T32 DK007328NIGMS NIH HHS F31 GM125363NIGMS NIH HHS R01 GM117407NIGMS NIH HHS R01 GM130764NIGMS NIH HHS R35 GM119793NIGMS NIH HHS R35 GM124717NIGMS NIH HHS R35 GM127049NIH HHS P40 OD018537
6 · The paper itself

Abstract

Because old age is associated with defects in circadian rhythm, loss of circadian regulation is thought to be pathogenic and contribute to mortality. We show instead that loss of specific circadian clock components Period (Per) and Timeless (Tim) in male Drosophila significantly extends lifespan. This lifespan extension is not mediated by canonical diet-restriction longevity pathways but is due to altered cellular respiration via increased mitochondrial uncoupling. Lifespan extension of per mutants depends on mitochondrial uncoupling in the intestine. Moreover, upregulated uncoupling protein UCP4C in intestinal stem cells and enteroblasts is sufficient to extend lifespan and preserve proliferative homeostasis in the gut with age. Consistent with inducing a metabolic state that prevents overproliferation, mitochondrial uncoupling drugs also extend lifespan and inhibit intestinal stem cell overproliferation due to aging or even tumorigenesis. These results demonstrate that circadian-regulated intestinal mitochondrial uncoupling controls longevity in Drosophila and suggest a new potential anti-aging therapeutic target.

Indexed as

Circadian RhythmAnimalsCarcinogenesisCell ProliferationCircadian ClocksCRISPR-Cas SystemsDrosophila melanogasterDrosophila ProteinsHomeostasisIntestinesLongevityMaleMembrane Potential, MitochondrialMembrane Transport ProteinsMitochondriaMutationDrosophila ProteinsMembrane Transport ProteinsPeriod Circadian ProteinsPER protein, Drosophilatim protein, DrosophilaUCP4C protein, DrosophilaUncoupling Protein 1

Identifiers

PMID32317636
PMCPMC7174288

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Registered trials

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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.