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The separate axes of TECPR1 and ATG16L1 in CASM
Centre for Cancer Cell Reprogramming, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Centre for Cancer Cell Reprogramming, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
2024 (English)In: Autophagy, ISSN 1554-8627, E-ISSN 1554-8635, Vol. 20, no 1, p. 214-215Article in journal (Refereed) Published
Abstract [en]

Conjugation of ATG8 to single membranes (CASM) is a fundamental cellular process that entails the conjugation of mammalian Atg8 homologs, here referred to as ATG8, to phosphatidylethanolamine (PE) and phosphatidylserine (PS) on endolysosomal compartments. Our current research, together with recent reports from the Randow, Wu, and Wileman labs, has uncovered yet another layer to this process. We discovered that, in addition to ATG16L1-containing complexes, TECPR1 (tectonin beta-propeller repeat containing 1)-containing ATG12–ATG5 E3 complexes can facilitate CASM, thereby providing a broader understanding of this pathway.

Place, publisher, year, edition, pages
Taylor & Francis Group, 2024. Vol. 20, no 1, p. 214-215
Keywords [en]
CASM, DysF, membrane damage, non-canonical autophagy, SopF, sphingomyelin
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-214413DOI: 10.1080/15548627.2023.2255462ISI: 001063992100001PubMedID: 37676042Scopus ID: 2-s2.0-85169885096OAI: oai:DiVA.org:umu-214413DiVA, id: diva2:1798227
Note

Published online: 07 Sep 2023.

Available from: 2023-09-18 Created: 2023-09-18 Last updated: 2024-01-15Bibliographically approved

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Carlsson, Sven R.

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