Evidence map›Paper›PMID 26154057›Full record

ArticleCell metabolism2015

The Deubiquitylase MATH-33 Controls DAF-16 Stability and Function in Metabolism and Longevity.

Thomas Heimbucher, Zheng Liu, Carine Bossard, Richard McCloskey, Andrea C Carrano, Christian G Riedel, Bogdan Tanasa, Christian Klammt, Bryan R Fonslow, Celine E Riera and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

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  3. Pelota-mediated ribosome-associated quality control counteracts aging and age-associated pathologies across species.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  10. Ubiquitin-related processes and innate immunity in C. elegans.Cellular and molecular life sciences : CMLS · 2021
    Review
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  13. USP7 regulates ALS-associated proteotoxicity and quality control through the NEDD4L-SMAD pathway.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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  15. Review
  16. Article
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  18. Extension of C. elegans lifespan using the ·NO-delivery dinitrosyl iron complexes.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2018
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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

16 authors at 7 institutions in 2 countries.

Thomas HeimbucherMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Molecular and Cell Biology Laboratory, Glenn Center for Aging Research, La Jolla, CA 92037, USA.
Zheng LiuMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Carine BossardMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Richard McCloskeyDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853-2703, USA.
Andrea C CarranoMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Christian G RiedelEuropean Research Institute for the Biology of Aging, University of Groningen, Groningen FA509713 AV, the Netherlands.
Bogdan TanasaDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Christian KlammtNomis Center for Immunobiology and Microbial Pathogenesis, Waitt Advanced Biophotonics Center, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Bryan R FonslowDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Celine E RieraMolecular and Cell Biology Department, University of California, Berkeley, CA 94705, USA.
Bjorn F LillemeierNomis Center for Immunobiology and Microbial Pathogenesis, Waitt Advanced Biophotonics Center, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Kenneth KemphuesDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853-2703, USA.
John R YatesDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Clodagh O'SheaMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Tony HunterMolecular and Cell Biology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA. Electronic address: hunter@salk.edu.
Andrew DillinMolecular and Cell Biology Department, University of California, Berkeley, CA 94705, USA; Howard Hughes Medical Institute, University of California, Berkeley, CA 94705, USA. Electronic address: dillin@berkeley.edu.
Salk Institute for Biological Studies · USCornell University · USScripps Research Institute · USHoward Hughes Medical Institute · USUniversity of California, Berkeley · USUniversity of California San Diego · USUniversity of Groningen · NL

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
SOMATIC CELL CYCLE REGULATION BY PHOSPHORYLATIONR01CA080100 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HUNTER, TONY R. · 1999 to 2018
$13.1M
SIGNAL TRANSDUCTION BY TYROSINE PHOSPHORYLATIONR01CA082683 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HUNTER, TONY R. · 1999 to 2019
$12.2M
Neuroendocrine Coordination of Mitochondrial Stress Signaling and ProteostasisR01ES021667 · NIEHS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DILLIN, ANDREW G · 2012 to 2023
$4.6M
Defining Critical p53 Therapeutic Targets and MechanismsR01CA137094 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI O'SHEA, CLODAGH · 2009 to 2019
$4.1M
Decipher membrane patterns in situ with super-resolution and dynamic microscopyDP2GM105455 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LILLEMEIER, BJOERN F · 2012 to 2012
$2.9M
Genetic Regulation of the Response to Dietary RestrictionR01AG027463 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI DILLIN, ANDREW G · 2008 to 2012
$2.4M
Specifying Insulin/IGF-1 Signaling in C. elegansR01DK070696 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI DILLIN, ANDREW G · 2005 to 2009
$1.9M
Nanoscale regulation of store-operated calcium entry through STIM-ORAI signallingR01GM110397 · NIGMS · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HOGAN, PATRICK, LILLEMEIER, BJOERN F · 2014 to 2017
$1.4M
Genome Sequencer FLXS10RR029668 · NCRR · UNIVERSITY OF CALIFORNIA BERKELEY · PI NGAI, JOHN J. · 2010 to 2010
$623k
Illumina Sequencer to Facilitate Functional Genomics at BerkeleyS10RR027303 · NCRR · UNIVERSITY OF CALIFORNIA BERKELEY · PI TAYLOR, JOHN W. · 2010 to 2010
$500k
Howard Hughes Medical InstituteNCI NIH HHS CA014195NCI NIH HHS CA082683NCI NIH HHS P30 CA014195NCI NIH HHS R01 CA080100NCI NIH HHS R01CA080100NCI NIH HHS R01 CA082683NCI NIH HHS R01 CA137094NCRR NIH HHS S10 RR027303NCRR NIH HHS S10RR027303NCRR NIH HHS S10 RR029668NCRR NIH HHS S10RR029668NIA NIH HHS R01 AG027463NIA NIH HHS R01AG027463NIDDK NIH HHS R01 DK070696NIDDK NIH HHS R01DK070696NIEHS NIH HHS R01 ES021667NIEHS NIH HHS R01ES021667NIGMS NIH HHS DP2 GM105455NIGMS NIH HHS R01 GM110397
6 · The paper itself

Abstract

FOXO family transcription factors are downstream effectors of Insulin/IGF-1 signaling (IIS) and major determinants of aging in organisms ranging from worms to man. The molecular mechanisms that actively promote DAF16/FOXO stability and function are unknown. Here we identify the deubiquitylating enzyme MATH-33 as an essential DAF-16 regulator in IIS, which stabilizes active DAF-16 protein levels and, as a consequence, influences DAF-16 functions, such as metabolism, stress response, and longevity in C. elegans. MATH-33 associates with DAF-16 in cellulo and in vitro. MATH-33 functions as a deubiquitylase by actively removing ubiquitin moieties from DAF-16, thus counteracting the action of the RLE-1 E3-ubiquitin ligase. Our findings support a model in which MATH-33 promotes DAF-16 stability in response to decreased IIS by directly modulating its ubiquitylation state, suggesting that regulated oscillations in the stability of DAF-16 protein play an integral role in controlling processes such as metabolism and longevity.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEndopeptidasesForkhead Transcription FactorsInsulinInsulin-Like Growth Factor ILongevityProtein StabilitySignal TransductionUbiquitinationCaenorhabditis elegans Proteinsdaf-16 protein, C elegansEndopeptidasesForkhead Transcription FactorsInsulinInsulin-Like Growth Factor IMATH-33 protein, C elegans

Identifiers

PMID26154057
PMCPMC4502596
OpenAlexW1565259657

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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.