Evidence map›Paper›PMID 32430326›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

β-Oxidation and autophagy are critical energy providers during acute glucose depletion in S

Carmen A Weber, Karthik Sekar, Jeffrey H Tang, Philipp Warmer, Uwe Sauer, Karsten Weis

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
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  5. Article
  6. bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Engineering yeast for tailored fatty acid profiles.Applied microbiology and biotechnology · 2025
    Review
  10. Article
  11. Article
  12. Microbial life in slow and stopped lanes.Trends in microbiology · 2024
    Review
  13. Article
  14. Contrasting views on the role of AMPK in autophagy.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

6 authors.

Carmen A WeberDepartment of Biology, Institute of Biochemistry, ETH (Eidgenössische Technische Hochschule) Zurich, 8093 Zurich, Switzerland.ORCID 0000-0002-9425-9771
Karthik SekarDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, 8093 Zurich, Switzerland.ORCID 0000-0003-2045-9364
Jeffrey H TangDepartment of Biology, Institute of Biochemistry, ETH (Eidgenössische Technische Hochschule) Zurich, 8093 Zurich, Switzerland.
Philipp WarmerDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, 8093 Zurich, Switzerland.
Uwe SauerDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, 8093 Zurich, Switzerland.
Karsten WeisDepartment of Biology, Institute of Biochemistry, ETH (Eidgenössische Technische Hochschule) Zurich, 8093 Zurich, Switzerland; karsten.weis@bc.biol.ethz.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to tolerate and thrive in diverse environments is paramount to all living organisms, and many organisms spend a large part of their lifetime in starvation. Upon acute glucose starvation, yeast cells undergo drastic physiological and metabolic changes and reestablish a constant-although lower-level of energy production within minutes. The molecules that are rapidly metabolized to fuel energy production under these conditions are unknown. Here, we combine metabolomics and genetics to characterize the cells' response to acute glucose depletion and identify pathways that ensure survival during starvation. We show that the ability to respire is essential for maintaining the energy status and to ensure viability during starvation. Measuring the cells' immediate metabolic response, we find that central metabolites drastically deplete and that the intracellular AMP-to-ATP ratio strongly increases within 20 to 30 s. Furthermore, we detect changes in both amino acid and lipid metabolite levels. Consistent with this, both bulk autophagy, a process that frees amino acids, and lipid degradation via β-oxidation contribute in parallel to energy maintenance upon acute starvation. In addition, both these pathways ensure long-term survival during starvation. Thus, our results identify bulk autophagy and β-oxidation as important energy providers during acute glucose starvation.

Indexed as

AutophagyEnergy MetabolismLipid MetabolismAdenosine TriphosphateAmino AcidsGene Expression Regulation, FungalGlucoseMetabolomicsOxidation-ReductionSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStarvationAdenosine TriphosphateAmino AcidsGlucoseSaccharomyces cerevisiae Proteinsacute glucose starvationlipidomicsmetabolomicsSaccharomyces cerevisiaeβ-oxidation

Identifiers

PMID32430326
PMCPMC7275744

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.