Evidence map›Paper›PMID 30679426›Full record

ArticleNature communications2019

LC3/GABARAPs drive ubiquitin-independent recruitment of Optineurin and NDP52 to amplify mitophagy.

Benjamin Scott Padman, Thanh Ngoc Nguyen, Louise Uoselis, Marvin Skulsuppaisarn, Lan K Nguyen, Michael Lazarou

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 2 pooled it
18.8field-weighted citation impact, top 1% 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

147 citing papers in PubMed, 2 syntheses or guidelines pooled it, 222 citations in OpenAlex.

  1. Pooled it
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  5. Selective autophagy in kidney health and disease.Nature reviews. Nephrology · 2026
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87 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Benjamin Scott PadmanDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia. Benjamin.Padman@monash.edu.ORCID http://orcid.org/0000-0002-5710-6100
Thanh Ngoc NguyenDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia.ORCID http://orcid.org/0000-0001-9698-0020
Louise UoselisDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia.ORCID http://orcid.org/0000-0001-8538-9817
Marvin SkulsuppaisarnDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia.ORCID http://orcid.org/0000-0003-4041-7014
Lan K NguyenDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia.ORCID http://orcid.org/0000-0003-4040-7705
Michael LazarouDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, 3800, Australia. Michael.Lazarou@monash.edu.ORCID http://orcid.org/0000-0003-2150-5545
Australian Regenerative Medicine Institute · AUDiscovery Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current models of selective autophagy dictate that autophagy receptors, including Optineurin and NDP52, link cargo to autophagosomal membranes. This is thought to occur via autophagy receptor binding to Atg8 homologs (LC3/GABARAPs) through an LC3 interacting region (LIR). The LIR motif within autophagy receptors is therefore widely recognised as being essential for selective sequestration of cargo. Here we show that the LIR motif within OPTN and NDP52 is dispensable for Atg8 recruitment and selectivity during PINK1/Parkin mitophagy. Instead, Atg8s play a critical role in mediating ubiquitin-independent recruitment of OPTN and NDP52 to growing phagophore membranes via the LIR motif. The additional recruitment of OPTN and NDP52 amplifies mitophagy through an Atg8-dependent positive feedback loop. Rather than functioning in selectivity, our discovery of a role for the LIR motif in mitophagy amplification points toward a general mechanism by which Atg8s can recruit autophagy factors to drive autophagosome growth and amplify selective autophagy.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid MotifsApoptosis Regulatory ProteinsAutophagosomesAutophagyAutophagy-Related Protein 8 FamilyCarrier ProteinsCell Cycle ProteinsHeLa CellsHumansMembrane Transport ProteinsMicrotubule-Associated ProteinsMitochondriaMitophagyNuclear ProteinsProtein BindingAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsAutophagy-Related Protein 8 FamilyCALCOCO2 protein, humanCarrier ProteinsCell Cycle ProteinsGABARAPL2 protein, humanGABARAP protein, humanMAP1LC3A protein, humanMembrane Transport ProteinsMicrotubule-Associated ProteinsNuclear ProteinsOPTN protein, humanparkin proteinProtein KinasesPTEN-Induced Putative KinaseTranscription Factor TFIIIAUbiquitinUbiquitin-Protein Ligases

Identifiers

PMID30679426
PMCPMC6345886
OpenAlexW2913143413

What OpenQuestion holds

Textmetadata
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.