Evidence map›Paper›PMID 37409490›Full record

ArticleThe EMBO journal2023

TECPR1 conjugates LC3 to damaged endomembranes upon detection of sphingomyelin exposure.

Keith B Boyle, Cara J Ellison, Paul R Elliott, Martina Schuschnig, Krista Grimes, Marc S Dionne, Chihiro Sasakawa, Sean Munro, Sascha Martens, Felix Randow

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
13.7field-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

52 citing papers in PubMed, 64 citations in OpenAlex.

  1. Emerging mechanisms of ATG8-independent non-canonical autophagy.Journal of physiology and biochemistry · 2026
    Review
  2. Review
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  8. Contradictory Effects on Hepatocytes in ASMD.International journal of molecular sciences · 2026
    Review
  9. Article
  10. Full length TECPR1 displays 'cis' Dysferlin domain architecture.bioRxiv : the preprint server for biology · 2026
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
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  19. ATG16L1 controls mammalian vacuolar proton ATPase.The Journal of cell biology · 2025
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Keith B BoyleDivision of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-0745-3964
Cara J EllisonDivision of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.
Paul R ElliottDivision of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.
Martina SchuschnigMax Perutz Labs, Vienna BioCenter (VBC), University of Vienna, Vienna, Austria.
Krista GrimesMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Marc S DionneMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.ORCID 0000-0002-8283-1750
Chihiro SasakawaMedical Mycology Research Center, Chiba University, Chiba, Japan.
Sean MunroDivision of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0001-6160-5773
Sascha MartensMax Perutz Labs, Vienna BioCenter (VBC), University of Vienna, Vienna, Austria.ORCID 0000-0003-3786-8199
Felix RandowDivision of Protein and Nucleic Acid Chemistry, MRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0003-0694-5315
MRC Laboratory of Molecular Biology · GBImperial College London · GBUniversity of Vienna · ATChiba University Hospital · JP

Funding

Austrian Science Fund FWF W 1261Medical Research Council MC_U105170648Medical Research Council MC_U105178783Wellcome Trust
6 · The paper itself

Abstract

Invasive bacteria enter the cytosol of host cells through initial uptake into bacteria-containing vacuoles (BCVs) and subsequent rupture of the BCV membrane, thereby exposing to the cytosol intraluminal, otherwise shielded danger signals such as glycans and sphingomyelin. The detection of glycans by galectin-8 triggers anti-bacterial autophagy, but how cells sense and respond to cytosolically exposed sphingomyelin remains unknown. Here, we identify TECPR1 (tectonin beta-propeller repeat containing 1) as a receptor for cytosolically exposed sphingomyelin, which recruits ATG5 into an E3 ligase complex that mediates lipid conjugation of LC3 independently of ATG16L1. TECPR1 binds sphingomyelin through its N-terminal DysF domain (N'DysF), a feature not shared by other mammalian DysF domains. Solving the crystal structure of N'DysF, we identified key residues required for the interaction, including a solvent-exposed tryptophan (W154) essential for binding to sphingomyelin-positive membranes and the conjugation of LC3 to lipids. Specificity of the ATG5/ATG12-E3 ligase responsible for the conjugation of LC3 is therefore conferred by interchangeable receptor subunits, that is, the canonical ATG16L1 and the sphingomyelin-specific TECPR1, in an arrangement reminiscent of certain multi-subunit ubiquitin E3 ligases.

Indexed as

Microtubule-Associated ProteinsSphingomyelinsAnimalsAutophagyAutophagy-Related Protein 5Autophagy-Related ProteinsCarrier ProteinsMammalsUbiquitin-Protein LigasesAutophagy-Related Protein 5Autophagy-Related ProteinsCarrier ProteinsMicrotubule-Associated ProteinsSphingomyelinsUbiquitin-Protein LigasesATG5-ATG12 E3 ligaseautophagyDysFmembrane damagesphingomyelin

Identifiers

PMID37409490
PMCPMC10476172
OpenAlexW4383302022

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.