O-mannosylation of misfolded proteins promotes ERAD
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ABSTRACT: Protein quality control (PQC) in the secretory pathway, a process critically linked to numerous human diseases, begins in the endoplasmic reticulum (ER) and involves ER-associated degradation (ERAD) of terminally misfolded proteins. In this study, we conducted genome-wide screens in baker's yeast (Saccharomyces cerevisiae) to investigate the degradation of Gas1*, a misfolded version of an O-mannosylated, glycosylphosphatidylinositol (GPI)-anchored protein. In combination with detailed biochemical and genetic analyses, these screens revealed an unexpected bifunctionality of the evolutionarily conserved heteromeric enzyme complex Pbn1-Gpi14: while it has been previously recognised as a GPI-mannosyltransferase, we here find that it catalyses the O-mannosylation of misfolded proteins, thereby
SUBMITTER: Leticia Lemus
PROVIDER: S-SCDT-10_1038-S44318-025-00647-2 | biostudies-other |
REPOSITORIES: biostudies-other
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