Evidence map›Paper›PMID 39509463›Full record

ArticleeLife2024

Autophagosome development and chloroplast segmentation occur synchronously for piecemeal degradation of chloroplasts.

Masanori Izumi, Sakuya Nakamura, Kohei Otomo, Hiroyuki Ishida, Jun Hidema, Tomomi Nemoto, Shinya Hagihara

Abstract read
In one paragraph

Article in eLife, 2024. 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. Review
  2. Review
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  4. PLETHORA-autophagy axis activates organ regeneration through ROS modulation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Review
  7. 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

7 authors.

Masanori IzumiFrontier Research Institute for Interdisciplinary Sciences (FRIS), Tohoku University, Sendai, Japan.ORCID https://orcid.org/0000-0001-5222-9163
Sakuya NakamuraCenter for Sustainable Resource Science (CSRS), RIKEN, Wako, Japan.ORCID https://orcid.org/0000-0002-8218-6894
Kohei OtomoExploratory Research Center on Life and Living Systems (ExCELLs), National Institutes of Natural Sciences, Okazaki, Japan.ORCID https://orcid.org/0000-0002-5322-6295
Hiroyuki IshidaGraduate School of Agricultural Science, Tohoku University, Sendai, Japan.ORCID https://orcid.org/0000-0002-8682-4566
Jun HidemaGraduate School of Life Sciences, Tohoku University, Sendai, Japan.ORCID https://orcid.org/0000-0002-3798-8257
Tomomi NemotoExploratory Research Center on Life and Living Systems (ExCELLs), National Institutes of Natural Sciences, Okazaki, Japan.ORCID https://orcid.org/0000-0001-6102-1495
Shinya HagiharaCenter for Sustainable Resource Science (CSRS), RIKEN, Wako, Japan.ORCID https://orcid.org/0000-0003-0348-7873

Funding

Japan Society for the Promotion of Science JP16H06280Japan Society for the Promotion of Science JP18H04852Japan Society for the Promotion of Science JP20H04916Japan Society for the Promotion of Science JP20H05352Japan Society for the Promotion of Science JP22H04627Japan Society for the Promotion of Science JP22H04660Joint Research by Exploratory Research Center on Life and Living Systems 20-314
6 · The paper itself

Abstract

Plants distribute many nutrients to chloroplasts during leaf development and maturation. When leaves senesce or experience sugar starvation, the autophagy machinery degrades chloroplast proteins to facilitate efficient nutrient reuse. Here, we report on the intracellular dynamics of an autophagy pathway responsible for piecemeal degradation of chloroplast components. Through live-cell monitoring of chloroplast morphology, we observed the formation of chloroplast budding structures in sugar-starved leaves. These buds were then released and incorporated into the vacuolar lumen as an autophagic cargo termed a Rubisco-containing body. The budding structures did not accumulate in mutants of core autophagy machinery, suggesting that autophagosome creation is required for forming chloroplast buds. Simultaneous tracking of chloroplast morphology and autophagosome development revealed that the isolation membranes of autophagosomes interact closely with part of the chloroplast surface before forming chloroplast buds. Chloroplasts then protrude at the site associated with the isolation membranes, which divide synchronously with autophagosome maturation. This autophagy-related division does not require DYNAMIN-RELATED PROTEIN 5B, which constitutes the division ring for chloroplast proliferation in growing leaves. An unidentified division machinery may thus fragment chloroplasts for degradation in coordination with the development of the chloroplast-associated isolation membrane.

Indexed as

ArabidopsisAutophagosomesAutophagyChloroplastsPlant LeavesArabidopsis ProteinsArabidopsis ProteinsA. thalianaautophagycell biologychloroplastplantplant biology

Identifiers

PMID39509463
PMCPMC11542923

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Registered trials

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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.