Evidence map›Paper›PMID 37917025›Full record

ArticleThe Journal of cell biology2023

The mechanism of Atg15-mediated membrane disruption in autophagy.

Yoko Kagohashi, Michiko Sasaki, Alexander I May, Tomoko Kawamata, Yoshinori Ohsumi

Abstract read
In one paragraph

Article in The Journal of cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
  5. The fate and function of theFrontiers in plant science · 2025
    Article
  6. Article
  7. Article
  8. 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

5 authors.

Yoko KagohashiResearch Center for Cell Biology, Institute of Innovative Research, Tokyo Institute of Technology , Yokohama, Japan.ORCID 0009-0002-9050-4570
Michiko SasakiResearch Center for Cell Biology, Institute of Innovative Research, Tokyo Institute of Technology , Yokohama, Japan.ORCID 0009-0001-0879-9334
Alexander I MayResearch Center for Cell Biology, Institute of Innovative Research, Tokyo Institute of Technology , Yokohama, Japan.ORCID 0000-0002-3758-1545
Tomoko KawamataResearch Center for Cell Biology, Institute of Innovative Research, Tokyo Institute of Technology , Yokohama, Japan.ORCID 0000-0002-3990-1194
Yoshinori OhsumiResearch Center for Cell Biology, Institute of Innovative Research, Tokyo Institute of Technology , Yokohama, Japan.ORCID 0000-0003-2384-2166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a lysosomal/vacuolar delivery system that degrades cytoplasmic material. During autophagy, autophagosomes deliver cellular components to the vacuole, resulting in the release of a cargo-containing autophagic body (AB) into the vacuole. AB membranes must be disrupted for degradation of cargo to occur. The lipase Atg15 and vacuolar proteases Pep4 and Prb1 are known to be necessary for this disruption and cargo degradation, but the mechanistic underpinnings remain unclear. In this study, we establish a system to detect lipase activity in the vacuole and show that Atg15 is the sole vacuolar phospholipase. Pep4 and Prb1 are required for the activation of Atg15 lipase function, which occurs following delivery of Atg15 to the vacuole by the MVB pathway. In vitro experiments reveal that Atg15 is a phospholipase B of broad substrate specificity that is likely implicated in the disruption of a range of membranes. Further, we use isolated ABs to demonstrate that Atg15 alone is able to disrupt AB membranes.

Indexed as

AutophagosomesAutophagyAutophagy-Related ProteinsPhospholipasesVacuolesCell MembraneLipaseAutophagy-Related ProteinsLipasePhospholipases

Identifiers

PMID37917025
PMCPMC10622257

What OpenQuestion holds

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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.