Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26

Guder, Philipp; Lotz-Havla, Amelie S.; Woidy, Mathias; Reiss, Dunja D.; Danecka, Marta K.; Schatz, Ulrich A.; Becker, Marc; Ensenauer, Regina; Pagel, Philipp; Buettner, Lars; Muntau, Ania C. und Gersting, Soren W. (2019): Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26. In: Biochimica et Biophysica Acta-Molecular Cell Research, Bd. 1866, Nr. 3: S. 518-531

Abstract

Peroxisomal biogenesis factor PEX26 is a membrane anchor for the multi-subunit PEX1-PEX6 protein complex that controls ubiquitination and dislocation of PEX5 cargo receptors for peroxisomal matrix protein import. PEX26 associates with the peroxisomal translocation pore via PEX14 and a splice variant (PEX26 Delta ex5) of unknown function has been reported. Here, we demonstrate PEX26 homooligomerization mediated by two heptad repeat domains adjacent to the transmembrane domain. We show that isoform-specific domain organization determines PEX26 oligomerization and impacts peroxisomal beta-oxidation and proliferation. PEX26 and PEX26 Delta ex5 displayed different patterns of interaction with PEX2-PEX10 or PEX13-PEX14 complexes, which relate to distinct pre-peroxisomes in the de novo synthesis pathway. Our data support an alternative PEX14-dependent mechanism of peroxisomal membrane association for the splice variant, which lacks a transmembrane domain. Structure-function relationships of PEX26 isoforms explain an extended function in peroxisomal homeostasis and these findings may improve our understanding of the broad phenotype of PEX26-associated human disorders.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 0167-4889
• Sprache: Englisch