Evidence map›Paper›PMID 32084377›Full record

ArticleCell metabolism2020

A Conserved Mito-Cytosolic Translational Balance Links Two Longevity Pathways.

Marte Molenaars, Georges E Janssens, Evan G Williams, Aldo Jongejan, Jiayi Lan, Sylvie Rabot, Fatima Joly, Perry D Moerland, Bauke V Schomakers, Marco Lezzerini and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 124 citations in OpenAlex.

  1. Trial
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  7. Perturbation of mitochondrial CaStress biology · 2026
    Article
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  9. Suppression rather than activation of the integrated stress response (GCN2-ATF4) pathway extends lifespan in the fly.Proceedings of the National Academy of Sciences of the United States of America · 2026
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13 more citing papers are in PubMed but not listed here.

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

18 authors at 8 institutions in 5 countries.

Marte MolenaarsLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Georges E JanssensLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Evan G WilliamsInstitute of Molecular Systems Biology, ETH Zurich, Zürich, Switzerland.
Aldo JongejanBioinformatics Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Jiayi LanInstitute of Molecular Systems Biology, ETH Zurich, Zürich, Switzerland.
Sylvie RabotMicalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Fatima JolyMicalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Perry D MoerlandBioinformatics Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Bauke V SchomakersLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands; Core Facility Metabolomics, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Marco LezzeriniLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Yasmine J LiuLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Mark A McCormickDepartment of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA; Autophagy, Inflammation, and Metabolism Center of Biological Research Excellence, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Brian K KennedyBuck Institute for Research on Aging, Novato, CA, USA; Departments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Michel van WeeghelLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands; Core Facility Metabolomics, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Antoine H C van KampenBioinformatics Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Ruedi AebersoldInstitute of Molecular Systems Biology, ETH Zurich, Zürich, Switzerland; Faculty of Science, University of Zürich, Switzerland.
Alyson W MacInnesLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Riekelt H HoutkooperLaboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands. Electronic address: r.h.houtkooper@amsterdamumc.nl.
University of Amsterdam · NLAmsterdam University Medical Centers · NLETH Zurich · CHAgroParisTech · FRNational University of Singapore · SGUniversité Paris-Saclay · FRUniversity of New Mexico · USUniversity of Zurich · CH

Funding

Unfolded Protein Response and Autophagy in T Helper Cell Effector FunctionP20GM121176 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Judy Lin Cannon · 2017 to 2026
$24.9M
Identifying Biomolecular Networks Driving Metabolic Trait VariationF32GM119190 · NIGMS · SWISS FEDERAL INST OF TECH (ETH ZURICH) · PI WILLIAMS, EVAN GRAEHL · 2016 to 2018
$174k
NIGMS NIH HHS F32 GM119190NIGMS NIH HHS P20 GM121176
6 · The paper itself

Abstract

Slowing down translation in either the cytosol or the mitochondria is a conserved longevity mechanism. Here, we found a non-interventional natural correlation of mitochondrial and cytosolic ribosomal proteins (RPs) in mouse population genetics, suggesting a translational balance. Inhibiting mitochondrial translation in C. elegans through mrps-5 RNAi repressed cytosolic translation. Transcriptomics integrated with proteomics revealed that this inhibition specifically reduced translational efficiency of mRNAs required in growth pathways while increasing stress response mRNAs. The repression of cytosolic translation and extension of lifespan from mrps-5 RNAi were dependent on atf-5/ATF4 and independent from metabolic phenotypes. We found the translational balance to be conserved in mammalian cells upon inhibiting mitochondrial translation pharmacologically with doxycycline. Lastly, extending this in vivo, doxycycline repressed cytosolic translation in the livers of germ-free mice. These data demonstrate that inhibiting mitochondrial translation initiates an atf-5/ATF4-dependent cascade leading to coordinated repression of cytosolic translation, which could be targeted to promote longevity.

Indexed as

LongevityProtein BiosynthesisSignal TransductionAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCytosolDoxycyclineMice, Inbred C57BLMitochondriaPhenotypeProteomeRibosomal ProteinsRNA InterferenceStress, PhysiologicalTranscription FactorsCaenorhabditis elegans ProteinsDoxycyclineProteomeRibosomal ProteinsTranscription FactorsagingATF4cytosolic translationdoxycyclinelongevitymitochondrial translationpolysomeribosomestranslational balancetranslational efficiency

Identifiers

PMID32084377
PMCPMC7214782
OpenAlexW3009017097

What OpenQuestion holds

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Read underepoch 390

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.