Evidence map›Paper›PMID 32986716›Full record

ArticlePLoS genetics2020

Snf1 AMPK positively regulates ER-phagy via expression control of Atg39 autophagy receptor in yeast ER stress response.

Tomoaki Mizuno, Kei Muroi, Kenji Irie

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Core principles of autophagy initiation mechanisms.Nature structural & molecular biology · 2026
    Review
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  6. Omic AI reveals new autophagy regulators from the Atg1 interactome inFrontiers in cell and developmental biology · 2025
    Article
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  8. The p53 target DRAM1 modulates calcium homeostasis and ER stress by promoting contact between lysosomes and the ER through STIM1.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Methods to Monitor Nucleophagy in Yeast.Methods in molecular biology (Clifton, N.J.) · 2024
    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

3 authors at 1 institution in 1 country.

Tomoaki MizunoDepartment of Molecular Cell Biology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID 0000-0002-6630-5363
Kei MuroiDepartment of Molecular Cell Biology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID 0000-0002-6752-4648
Kenji IrieDepartment of Molecular Cell Biology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID 0000-0001-6364-1487
University of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a fundamental process responsible for degradation and recycling of intracellular contents. In the budding yeast, non-selective macroautophagy and microautophagy of the endoplasmic reticulum (ER) are caused by ER stress, the circumstance where aberrant proteins accumulate in the ER. The more recent study showed that protein aggregation in the ER initiates ER-selective macroautophagy, referred to as ER-phagy; however, the mechanisms by which ER stress induces ER-phagy have not been fully elucidated. Here, we show that the expression levels of ATG39, encoding an autophagy receptor specific for ER-phagy, are significantly increased under ER-stressed conditions. ATG39 upregulation in ER stress response is mediated by activation of its promoter, which is positively regulated by Snf1 AMP-activated protein kinase (AMPK) and negatively by Mig1 and Mig2 transcriptional repressors. In response to ER stress, Snf1 promotes nuclear export of Mig1 and Mig2. Our results suggest that during ER stress response, Snf1 mediates activation of the ATG39 promoter and consequently facilitates ER-phagy by negatively regulating Mig1 and Mig2.

Indexed as

AutophagyAutophagy-Related ProteinsEndoplasmic Reticulum StressGene Expression Regulation, FungalMicroorganisms, Genetically-ModifiedMitophagyMutationPhosphorylationPromoter Regions, GeneticProtein Serine-Threonine KinasesReceptors, Cytoplasmic and NuclearRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsAtg39 protein, S cerevisiaeAutophagy-Related ProteinsMIG1 protein, S cerevisiaeMig2 protein, S cerevisiaeProtein Serine-Threonine KinasesReceptors, Cytoplasmic and NuclearRepressor ProteinsSaccharomyces cerevisiae ProteinsSNF1-related protein kinases

Identifiers

PMID32986716
PMCPMC7544123
OpenAlexW3090100347

What OpenQuestion holds

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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.