Peroxisomal core structures segregate diverse metabolic pathways
Peroxisomes are single membrane-bounded oxidative organelles with various metabolic functions including β-oxidation of fatty acids. Peroxisomes of many species confine certain metabolic enzymes into sub-compartments sometimes visible as electron dense cores. Why these structures form is largely unknown. Here, we report that in the smut fungus Ustilago maydis detergent resistant core structures are enriched for different enzymes excluding several key enzymes of the β-oxidation pathway. This confinement contributes to generation of peroxisome subpopulations that differ in their enzyme content. We identify short amino acid motifs necessary and sufficient for protein self-assembly into aggregates in vitro. The motifs trigger enrichment in cores in vivo and are active in mammalian cells. Perturbation of core assembly via variation of such motifs affects peroxisome function in U. maydis strains challenged with fatty acids. Thus, protein core structures serve to compartmentalize the lumen of peroxisomes thereby preventing interference of biochemical reactions. Metabolic compartmentalization of peroxisomes via assembly of specific proteins may occur in other organisms as well.
Authors
- Nils Bäcker
- Christopher-Nils Mais (ORCID: https://orcid.org/0000-0003-1927-2885)
- Christian CR Renicke (ORCID: https://orcid.org/0000-0003-3226-9840)
- Domenica Martorana
- Thomas Heimerl
- Julia Ast (ORCID: https://orcid.org/0000-0002-0039-4762)
- Gert Bange (ORCID: https://orcid.org/0000-0002-7826-0932)
- Björn Sandrock (ORCID: https://orcid.org/0000-0002-0478-2877)
- Jan Pané‐Farré (ORCID: https://orcid.org/0000-0003-2723-2568)
- Christof Taxis (ORCID: https://orcid.org/0000-0001-5952-7091)
- Valentin Wernet (ORCID: https://orcid.org/0000-0002-3747-6171)
- Marvin Christ
- Michael Bölker (ORCID: https://orcid.org/0000-0002-7366-3855)
- James D. Berger
- Johannes Freitag (ORCID: https://orcid.org/0000-0002-8251-4878)
- Kay Oliver Schink (ORCID: https://orcid.org/0000-0002-5903-4059)
- Thorsten Stehlik (ORCID: https://orcid.org/0000-0002-1097-244X)
- Judith M. Klatt
Institutions
- Oslo University Hospital (NO)
- Philipps University of Marburg (DE)
- University of Oslo (NO)
- University of Erfurt (DE)
- Norwegian Cancer Society (NO)
- Cancer Registry of Norway (NO)
- Loewe Center for Synthetic Microbiology (DE)
- Max Planck Institute for Terrestrial Microbiology (DE)
- Stanford University (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-02-20
- DOI
- https://doi.org/10.1038/s41467-025-57053-9
- Citations
- 4
- Primary Topic
- Peroxisome Proliferator-Activated Receptors
- Type
- article
- Field-Weighted Citation Impact
- 3.22
Funders
- Philipps-Universität Marburg
- Deutsche Forschungsgemeinschaft
- Norges Forskningsråd
- Helse Sør-Øst RHF