Evidence map›Paper›PMID 29519802›Full record

ArticleThe Journal of cell biology2018

Autophagy balances mtDNA synthesis and degradation by DNA polymerase POLG during starvation.

Tânia Catarina Medeiros, Ryan Lee Thomas, Ruben Ghillebert, Martin Graef

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
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  6. NADCells · 2025
    Review
  7. Review
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  9. Review
  10. Review
  11. Flow-cytometry reveals mitochondrial DNA accumulation inFrontiers in cell and developmental biology · 2024
    Article
  12. Article
  13. The Fate of Oxidative Strand Breaks in Mitochondrial DNA.Antioxidants (Basel, Switzerland) · 2023
    Article
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Tânia Catarina MedeirosMax Planck Institute for Biology of Ageing, Cologne, Germany.
Ryan Lee ThomasMax Planck Institute for Biology of Ageing, Cologne, Germany.
Ruben GhillebertMax Planck Institute for Biology of Ageing, Cologne, Germany.ORCID 0000-0002-0747-7499
Martin GraefMax Planck Institute for Biology of Ageing, Cologne, Germany martin.graef@age.mpg.de.ORCID 0000-0002-6820-1533
Max Planck Institute for Biology of Ageing · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria contain tens to thousands of copies of their own genome (mitochondrial DNA [mtDNA]), creating genetic redundancy capable of buffering mutations in mitochondrial genes essential for cellular function. However, the mechanisms regulating mtDNA copy number have been elusive. Here we found that DNA synthesis and degradation by mtDNA polymerase γ (POLG) dynamically controlled mtDNA copy number in starving yeast cells dependent on metabolic homeostasis provided by autophagy. Specifically, the continuous mtDNA synthesis by POLG in starving wild-type cells was inhibited by nucleotide insufficiency and elevated mitochondria-derived reactive oxygen species in the presence of autophagy dysfunction. Moreover, after prolonged starvation, 3'-5' exonuclease-dependent mtDNA degradation by POLG adjusted the initially increasing mtDNA copy number in wild-type cells, but caused quantitative mtDNA instability and irreversible respiratory dysfunction in autophagy-deficient cells as a result of nucleotide limitations. In summary, our study reveals that mitochondria rely on the homeostatic functions of autophagy to balance synthetic and degradative modes of POLG, which control copy number dynamics and stability of the mitochondrial genome.

Indexed as

AutophagyDNA, MitochondrialDNA Polymerase gammaGene DosageModels, BiologicalMutationNucleotidesReactive Oxygen SpeciesSaccharomyces cerevisiaeDNA, MitochondrialDNA Polymerase gammaNucleotidesPOLG protein, humanReactive Oxygen Species

Identifiers

PMID29519802
PMCPMC5940314
OpenAlexW2791353847

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.