Evidence map›Paper›PMID 37724628›Full record

ArticleEMBO reports2023

The fruit fly acetyltransferase chameau promotes starvation resilience at the expense of longevity.

Anuroop Venkateswaran Venkatasubramani, Toshiharu Ichinose, Mai Kanno, Ignasi Forne, Hiromu Tanimoto, Shahaf Peleg, Axel Imhof

Abstract read
In one paragraph

Article in EMBO reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

7 authors.

Anuroop Venkateswaran VenkatasubramaniDepartment of Molecular Biology, Biomedical Center Munich, Faculty of Medicine, LMU Munich, Martinsried, Germany.ORCID 0000-0003-2119-8741
Toshiharu IchinoseGraduate School of Life Sciences, Tohoku University, Sendai, Japan.
Mai KannoGraduate School of Life Sciences, Tohoku University, Sendai, Japan.
Ignasi ForneProtein Analysis Unit, Faculty of Medicine, Biomedical Center Munich, LMU Munich, Martinsried, Germany.ORCID 0000-0003-0309-907X
Hiromu TanimotoGraduate School of Life Sciences, Tohoku University, Sendai, Japan.
Shahaf PelegResearch Group Epigenetics, Metabolism and Longevity, Institute for Farm Animal Biology, Dummerstorf, Germany.ORCID 0000-0003-2646-3807
Axel ImhofDepartment of Molecular Biology, Biomedical Center Munich, Faculty of Medicine, LMU Munich, Martinsried, Germany.ORCID 0000-0003-2993-8249

Funding

Deutsche Forschungsgemeinschaft (DFG) 213249687Deutsche Forschungsgemeinschaft (DFG) 325871075Deutsche Forschungsgemeinschaft (DFG) 458246576Impetus grant from the Norn groupLeibniz-Institut für Nutztierbiologie (FBN)
6 · The paper itself

Abstract

Proteins involved in cellular metabolism and molecular regulation can extend lifespan of various organisms in the laboratory. However, any improvement in aging would only provide an evolutionary benefit if the organisms were able to survive under non-ideal conditions. We have previously shown that Drosophila melanogaster carrying a loss-of-function allele of the acetyltransferase chameau (chm) has an increased healthy lifespan when fed ad libitum. Here, we show that loss of chm and reduction in its activity results in a substantial reduction in weight and a decrease in starvation resistance. This phenotype is caused by failure to properly regulate the genes and proteins required for energy storage and expenditure. The previously observed increase in survival time thus comes with the inability to prepare for and cope with nutrient stress. As the ability to survive in environments with restricted food availability is likely a stronger evolutionary driver than the ability to live a long life, chm is still present in the organism's genome despite its apparent negative effect on lifespan.

Indexed as

AcetyltransferasesDrosophila melanogasterDrosophila ProteinsLongevityStarvationAnimalsPhenotypeAcetyltransferasesDrosophila ProteinsacetylationchameauDrosophilaHBO1starvation

Identifiers

PMID37724628
PMCPMC10561354

What OpenQuestion holds

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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.