Evidence map›Paper›PMID 26781291›Full record

ArticleEMBO reports2016

Life span extension by targeting a link between metabolism and histone acetylation in Drosophila.

Shahaf Peleg, Christian Feller, Ignasi Forne, Evelyn Schiller, Daniel C Sévin, Tamas Schauer, Catherine Regnard, Tobias Straub, Matthias Prestel, Caroline Klima and 7 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
10.2field-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

77 citing papers in PubMed, 134 citations in OpenAlex.

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  19. Lysine-36 ofbioRxiv : the preprint server for biology · 2023
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17 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

17 authors at 5 institutions in 2 countries.

Shahaf PelegDepartment of Physiological Chemistry, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Department of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Christian FellerDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Ignasi ForneDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Protein Analysis Unit, Biomedical Center, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Evelyn SchillerInstitute of Experimental Genetics, Helmholtz Zentrum Munich, German Research Center for Environment and Health (GmbH), Neuherberg, Germany.
Daniel C SévinInstitute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland PhD Program on Systems Biology, Life Science Zürich, Zürich, Switzerland.
Tamas SchauerDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Catherine RegnardDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Tobias StraubDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Bioinformatics Unit, Biomedical Center, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Matthias PrestelDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Caroline KlimaDepartment of Physiological Chemistry, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Department of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Melanie Schmitt NogueiraDepartment of Physiological Chemistry, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Department of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Lore BeckerInstitute of Experimental Genetics, Helmholtz Zentrum Munich, German Research Center for Environment and Health (GmbH), Neuherberg, Germany.
Thomas KlopstockFriedrich-Baur-Institut, Department of Neurology, Ludwig-Maximilians University, Munich, Germany DZNE - German Center for Neurodegenerative Diseases, Munich, Germany Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
Uwe SauerInstitute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland.
Peter B BeckerDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany.
Axel ImhofDepartment of Molecular Biology, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Protein Analysis Unit, Biomedical Center, Ludwig-Maximilians University, Planegg-Martinsried, Germany Munich Cluster for Systems Neurology (SyNergy), Munich, Germany imhof@lmu.de andreas.ladurner@med.lmu.de.
Andreas G LadurnerDepartment of Physiological Chemistry, Biomedical Center and Center for Integrated Protein Science Munich, Ludwig-Maximilians University, Planegg-Martinsried, Germany Munich Cluster for Systems Neurology (SyNergy), Munich, Germany imhof@lmu.de andreas.ladurner@med.lmu.de.
Center for Integrated Protein Science Munich · DELudwig-Maximilians-Universität München · DEETH Zurich · CHHelmholtz Zentrum München · DEGerman Center for Neurodegenerative Diseases · DE

Funding

European Research Council 293948
6 · The paper itself

Abstract

Old age is associated with a progressive decline of mitochondrial function and changes in nuclear chromatin. However, little is known about how metabolic activity and epigenetic modifications change as organisms reach their midlife. Here, we assessed how cellular metabolism and protein acetylation change during early aging in Drosophila melanogaster. Contrary to common assumptions, we find that flies increase oxygen consumption and become less sensitive to histone deacetylase inhibitors as they reach midlife. Further, midlife flies show changes in the metabolome, elevated acetyl-CoA levels, alterations in protein-notably histone-acetylation, as well as associated transcriptome changes. Based on these observations, we decreased the activity of the acetyl-CoA-synthesizing enzyme ATP citrate lyase (ATPCL) or the levels of the histone H4 K12-specific acetyltransferase Chameau. We find that these targeted interventions both alleviate the observed aging-associated changes and promote longevity. Our findings reveal a pathway that couples changes of intermediate metabolism during aging with the chromatin-mediated regulation of transcription and changes in the activity of associated enzymes that modulate organismal life span.

Indexed as

LongevityProtein Processing, Post-TranslationalAcetylationAcetyltransferasesAnimalsATP Citrate (pro-S)-LyaseDrosophila melanogasterDrosophila ProteinsHistonesAcetyltransferasesATP Citrate (pro-S)-Lyasechm protein, DrosophilaDrosophila ProteinsHistonesacetylationageingchromatinmetabolism

Identifiers

PMID26781291
PMCPMC4772992
OpenAlexW2290069354

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.