The proximity interactome of <scp>PML</scp> isoforms I and <scp>II</scp> under fatty acid stress
Promyelocytic leukemia (PML) protein forms the scaffold for PML nuclear bodies (PML NB) that reorganize into Lipid-Associated PML Structures (LAPS) under fatty acid stress. We determined how the fatty acid oleate alters the interactome of PMLI or PMLII by expressing fusions with the ascorbate peroxidase APEX2 in U2OS cells. The resultant interactome included ESCRT and COPII transport protein nodes. Proximity ligation assay (PLA) revealed that COPII proteins SEC23B, SEC24A and USO1 preferentially associated with PML NBs. Nuclear localization of USO1, but not SEC23B and SEC24A, was reduced in PML knockout cells and restored by PMLII expression. Thus, proximity-labelling methods identified COPII transport protein interactions with PML NBs that are disrupted by fatty acid stress.
Authors
- Jayme Salsman (ORCID: https://orcid.org/0000-0001-9788-652X)
- François‐Michel Boisvert (ORCID: https://orcid.org/0000-0001-8882-8619)
- Graham Dellaire (ORCID: https://orcid.org/0000-0002-3466-6316)
- Jordan Thompson
- Neale D. Ridgway (ORCID: https://orcid.org/0000-0002-0441-6228)
- Dominique Lévesque (ORCID: https://orcid.org/0000-0001-7660-0457)
Institutions
- Dalhousie University (CA)
- Université de Sherbrooke (CA)
Publication Details
- Journal
- FEBS Letters
- Published
- 2024-12-20
- DOI
- https://doi.org/10.1002/1873-3468.15081
- Citations
- 3
- Primary Topic
- Retinoids in leukemia and cellular processes
- Type
- article
- Field-Weighted Citation Impact
- 0.70
Funders
- Cancer Research Institute
- Beatrice Hunter Cancer Research Institute
- Dalhousie University
- Canadian Institutes of Health Research
- Natural Sciences and Engineering Research Council of Canada
- Fonds de Recherche du Québec - Santé
- Institute of Nutrition, Metabolism and Diabetes