Evidence map›Paper›PMID 32896087›Full record

ArticleEMBO reports2020

Mitochondrial respiration is required to provide amino acids during fermentative proliferation of fission yeast.

Michal Malecki, Stephan Kamrad, Markus Ralser, Jürg Bähler

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Can Unicellular Organisms Sequester a Germline? The Yeast-Germline Hypothesis.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  7. Article
  8. Article
  9. InFrontiers in fungal biology · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Kinetic and Regulatory Properties ofInternational journal of molecular sciences · 2023
    Article
  18. Article
  19. Role of amino acid metabolism in mitochondrial homeostasis.Frontiers in cell and developmental biology · 2023
    Review
  20. Article
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

4 authors at 2 institutions in 2 countries.

Michal MaleckiInstitute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Warsaw, Poland.ORCID 0000-0002-1525-5036
Stephan KamradInstitute of Healthy Ageing and Research Department of Genetics, Evolution & Environment, University College London, London, UK.ORCID 0000-0002-5957-4661
Markus RalserMolecular Biology of Metabolism Laboratory, The Francis Crick Institute, London, UK.
Jürg BählerInstitute of Healthy Ageing and Research Department of Genetics, Evolution & Environment, University College London, London, UK.ORCID 0000-0003-4036-1532
The Francis Crick Institute · GBUniversity College London · GB

Funding

Foundation for Polish Science POIR.04.04.00-00-4316/17Wellcome Trust FC001134Wellcome Trust (WT) 095598/Z/11/Z
6 · The paper itself

Abstract

When glucose is available, many organisms repress mitochondrial respiration in favour of aerobic glycolysis, or fermentation in yeast, that suffices for ATP production. Fission yeast cells, however, rely partially on respiration for rapid proliferation under fermentative conditions. Here, we determined the limiting factors that require respiratory function during fermentation. When inhibiting the electron transport chain, supplementation with arginine was necessary and sufficient to restore rapid proliferation. Accordingly, a systematic screen for mutants growing poorly without arginine identified mutants defective in mitochondrial oxidative metabolism. Genetic or pharmacological inhibition of respiration triggered a drop in intracellular levels of arginine and amino acids derived from the Krebs cycle metabolite alpha-ketoglutarate: glutamine, lysine and glutamic acid. Conversion of arginine into these amino acids was required for rapid proliferation when blocking the respiratory chain. The respiratory block triggered an immediate gene expression response diagnostic of TOR inhibition, which was muted by arginine supplementation or without the AMPK-activating kinase Ssp1. The TOR-controlled proteins featured biased composition of amino acids reflecting their shortage after respiratory inhibition. We conclude that respiration supports rapid proliferation in fermenting fission yeast cells by boosting the supply of Krebs cycle-derived amino acids.

Indexed as

SchizosaccharomycesAmino AcidsCell ProliferationFermentationRespirationAmino Acidsargininecellular metabolismfermentationrespirationS. pombe

Identifiers

PMID32896087
PMCPMC7645267
OpenAlexW3084357471

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.