Evidence map›Paper›PMID 36184612›Full record

ArticleAutophagy2023

The Cys-N-degron pathway modulates pexophagy through the N-terminal oxidation and arginylation of ACAD10.

Sang Mi Shim, Ha Rim Choi, Soon Chul Kwon, Hye Yeon Kim, Ki Woon Sung, Eui Jung Jung, Su Ran Mun, Tae Hyun Bae, Dong Hyun Kim, Yeon Sung Son and 5 more

Open access · greenAbstract read
In one paragraph

Article in Autophagy, 2023. 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
3.0field-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

20 citing papers in PubMed, 40 citations in OpenAlex.

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  7. ACAD10 and ACAD11 enable mammalian 4-hydroxy acid lipid catabolism.Nature structural & molecular biology · 2025
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  17. When autophagy meets placenta development and pregnancy complications.Frontiers in cell and developmental biology · 2024
    Review
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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

15 authors at 3 institutions in 1 country.

Sang Mi ShimDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Ha Rim ChoiDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Soon Chul KwonDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-7271-6284
Hye Yeon KimDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-8895-2396
Ki Woon SungDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Eui Jung JungDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Su Ran MunDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-5320-1135
Tae Hyun BaeDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Dong Hyun KimAnticancer Agents Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongwon, Korea.ORCID 0000-0002-7463-209X
Yeon Sung SonNeuroscience Research Institute, Medical Research Center, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Chan Hoon JungDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Jihoon LeeCellular Degradation Biology Center, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-6686-3974
Min Jae LeeDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-3252-6467
Joo-Won ParkDepartment of Biochemistry, College of Medicine, Ewha Womans University, Seoul, Republic of Korea.ORCID 0000-0002-9765-0477
Yong Tae KwonDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-8115-3150
Seoul National University · KREwha Womans University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the N-degron pathway, N-recognins recognize cognate substrates for degradation via the ubiquitin (Ub)-proteasome system (UPS) or the autophagy-lysosome system (hereafter autophagy). We have recently shown that the autophagy receptor SQSTM1/p62 (sequestosome 1) is an N-recognin that binds the N-terminal arginine (Nt-Arg) as an N-degron to modulate autophagic proteolysis. Here, we show that the N-degron pathway mediates pexophagy, in which damaged peroxisomal fragments are degraded by autophagy under normal and oxidative stress conditions. This degradative process initiates when the Nt-Cys of ACAD10 (acyl-CoA dehydrogenase family, member 10), a receptor in pexophagy, is oxidized into Cys sulfinic (Cys

Indexed as

AutophagyMacroautophagyAnimalsArginineCysteamineCysteineMiceReactive Oxygen SpeciesSequestosome-1 ProteinTransferasesUbiquitinArginineCysteamineCysteineReactive Oxygen SpeciesSequestosome-1 ProteinTransferasesUbiquitinAcyl-CoA dehydrogenase family, member 10N-degron pathwayoxidative stressperoxisomal biogenesis disordersperoxisomepexophagy

Identifiers

PMID36184612
PMCPMC10262816
OpenAlexW4300003476

What OpenQuestion holds

Textmetadata
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.